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Dr Stellios Arseniyadis

Stellios Arseniyadis

Reader in Organic Chemistry

School of Biological and Chemical Sciences
Room G.08, Joseph Priestley Building
+44 (0)20 7882 8445

www.sbcs.qmul.ac.uk/staff/stelliosarseniyadis.html

Research

Organic Chemistry

Research Interests

I am principally interested in the development of new synthetic methods to attain high structural and functional complexity. Methods lie within the areas of organocatalysis, transition metal catalysis and, more recently, bio-hybrid catalysis. In addition to that, I am interested in developing new drug-delivery devices by combining acoustics and microfluidics.

Find out more on our website

Research department

Chemistry and Biochemistry

Publications of specific relevance to Materials Research

Publications

2021

  • Selmi-Higashi E, Zhang J, Cambeiro XC and Arseniyadis S (2021). Synthesis of α-Difluoromethyl Aryl Ketones through a Photoredox Difluoromethylation of Enol Silanes. Organic Letters  vol. 23, (11) 4239-4243. 10.1021/acs.orglett.1c01177
  • Richard F, Mateos C and Arseniyadis S (2021). 4-Cyano-3-oxotetrahydrothiophene (c-THT): An Ideal Acrylonitrile Anion Equivalent. Synopen  vol. 5, (1) 10.1055/s-0040-1706019

2020

  • Kerim MDE, Katsina T, Cattoen M, Fincias N, Arseniyadis S and Kaim LE (2020). O-Allylated Pudovik and Passerini Adducts as Versatile Scaffolds for Product Diversification. American Chemical Society  Journal of Organic Chemistry  10.1021/acs.joc.0c01721
  • Katsina T, Clavier L, Giffard J-F, Macedo Portela da Silva N, Fournier J, Tamion R, Copin C, Arseniyadis S and Jean A (2020). Scalable Aerobic Oxidation of Alcohols Using Catalytic DDQ/HNO3. American Chemical Society  Organic Process Research and Development  10.1021/acs.oprd.9b00513
  • Mansot J, Lauberteaux J, Aurélien L, Marc M, Jean-Jacques V, Marcia de Figueiredo R, Arseniyadis S, Jean-Marc C and Smietana M (2020). DNA-Based Asymmetric Inverse Electron-Demand Hetero-Diels Alder. Wiley  Chemistry: a European Journal  10.1002/chem.202000516

2019

  • Katsina T, Sharma S, Buccafusca R, Quinn D, Moody T and Arseniyadis S (2019). A Sequential palladium‑catalyzed allylic alkylation/retro-Dieckmann fragmentation strategy for the synthesis of α-substituted acrylonitriles. American Chemical Society  Organic Letters  10.1021/acs.orglett.9b03522
  • Aubert S, Bezagu M, Spivey AC and Arseniyadis S (2019). Spatial and temporal control of chemical processes. Springer Science and Business Media Llc  Nature Reviews Chemistry  10.1038/s41570-019-0139-6
  • Duchemin N, Buccafusca R, Daumas M, Ferey V and Arseniyadis S (2019). A Unified Strategy for the Synthesis of Difluoromethyl- and Vinylfluoride-Containing Scaffolds. American Chemical Society (Acs)  Organic Letters  10.1021/acs.orglett.9b02887
  • Mansot J, Vasseur JJ, Arseniyadis S and Smietana M (2019). α,β‐Unsaturated 2‐Acyl‐Imidazoles in Asymmetric Biohybrid Catalysis. Wiley  Chemcatchem  10.1002/cctc.201900743
  • ARSENIYADIS S, Smietana M, DUCHEMIN N, AUBERT S, Mansot J and Vasseur J-J (2019). A rational quest for selectivity through precise ligand-positioning in the tandem DNA-catalysed Friedel-Crafts alkylation/asymmetric protonation. Royal Society of Chemistry  Chemical Science  (10) 10.1039/C8SC05543B
  • ARSENIYADIS S, AUBERT S and KATSINA S (2019). A Sequential Pd-AAA/Cross-Metathesis/Cope Rearrangement Strategy for the Stereoselective Synthesis of Chiral Butenolides. American Chemical Society  Organic Letters  10.1021/acs.orglett.9b00521
  • ARSENIYADIS S, Song T and Cossy J (2019). Asymmetric Synthesis of α-Quaternary γ-Lactams through Palladium-Catalyzed Asymmetric Allylic Alkylation. American Chemical Society  Organic Letters  10.1021/acs.orglett.8b03613

2018

  • ARSENIYADIS S and Smietana M (2018). Challenges and Opportunities in DNA-based Asymmetric Catalysis. Schweizerische Chemische Gesellschaft  Chimia  10.2533/chimia.2018.630
  • Benedetti E, Bressy C, Smietana M and Arseniyadis S (2018). Recent Applications of Kagan's Reagent (SmI2) in Natural Product Synthesis. Efficiency in Natural Product Total Synthesis  10.1002/9781118940228.ch6
  • Smietana M, Benedetti E, Bressy C and Arseniyadis S (2018). Multicomponent Reactions in Natural Product Synthesis. Efficiency in Natural Product Total Synthesis  10.1002/9781118940228.ch8
  • Duchemin N, Skiredj A, Mansot J, Leblanc K, Vasseur J, Beniddir MA, Evanno L, Poupon E, Smietana M and Arseniyadis S (2018). DNA‐Templated [2+2] Photocycloaddition: A Straightforward Entry into the Aplysinopsin Family of Natural Products. Angewandte Chemie  vol. 130, (36) 11960-11965. 10.1002/ange.201806357
  • ARSENIYADIS S, DUCHEMIN N, Skiredj A, Mansot J, Leblanc K, Vasseur J-J, Beniddir M, Evanno E, Poupon E and Smietana M (2018). DNA‐Templated [2 2] Photocycloaddition: A Straightforward Entry into the Aplysinopsin Family of Natural Products. Wiley  Angewandte Chemie International Edition  10.1002/anie.201806357
  • ARSENIYADIS S, Song T and Cossy J (2018). Highly Enantioselective, Base‐Free Synthesis of α‐Quaternary Succinimides through Catalytic Asymmetric Allylic Alkylation. Wiley  Chemistry - a European Journal  10.1002/chem.201800920
  • ARSENIYADIS S (2018). Palladium-catalyzed asymmetric allylic alkylation of 4-substituted isoxazolidin-5-ones: A straightforward access to b2,2-amino acids. Wiley  Chemistry - a European Journal  10.1002/chem.201800641
  • ARSENIYADIS S (2018). Dinucleating Schiff base ligand in Zn/4f coordination chemistry: synthetic challenges and catalytic activity evaluation. Royal Society of Chemistry  Dalton Transactions  10.1039/C8DT00538A
  • Kerim MD, Cattoen M, Fincias N, Dos¿Santos A, Arseniyadis S and El¿Kaïm L (2018). Palladium-catalysedO-Allylation of α-Hydroxyphosphonates: An Expedient Entry into Phosphono-oxaheterocycles. Wiley  Advanced Synthesis & Catalysis  vol. 360, (3) 449-454. 10.1002/adsc.201701150

2017

  • Dolé Kerim M, Cattoen M, Fincias N, Dos Santos A, Arseniyadis S and El Kaim L (2017). Palladium-catalysed O-Allylation of alpha-Hydroxyphosphonates: An Expedient entry into Phosphono-oxaheterocycles. Advanced Synthesis & Catalysis  10.1002/adsc.201701150
  • Duchemin N, Heath-Apostolopoulos I, Smietana M and Arseniyadis S (2017). A decade of DNA-hybrid catalysis: from innovation to comprehension. Org. Biomol. Chem.  10.1039/C7OB00176B
  • Arseniyadis S, Duchemin N and Smietana M (2017). Innovative DNA-based asymmetric catalysis. Actualite Chimique  (417) 17-27.
  • Bezagu M, Clarhaut J, Renoux B, Monti F, Tanter M, Tabeling P, Cossy J, Couture O, Papot S and Arseniyadis S (2017). In situ targeted activation of an anticancer agent using ultrasound-triggered release of composite droplets. European Journal of Medicinal Chemistry  10.1016/j.ejmech.2017.03.057
  • Nascimento de Oliveira M, Fournier J, Arseniyadis S and Cossy J (2017). A Palladium-Catalyzed Asymmetric Allylic Alkylation Approach to α-Quaternary γ-Butyrolactones. Organic Letters  vol. 19, (1) 14-17. 10.1021/acs.orglett.6b02971

2016

  • El Mamouni EH, Cattoen M, Cordier M, Cossy J, Arseniyadis S, Ilitki H and El Kaïm L (2016). Selective Tsuji–Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles. Chem. Commun.  vol. 52, (100) 14490-14493. 10.1039/C6CC08171A
  • Kolleth A, Gebauer J, ElMarrouni A, Lebeuf R, Prévost C, Brohan E, Arseniyadis S and Cossy J (2016). Total Synthesis of Putative 11-epi-Lyngbouilloside Aglycon. Frontiers Media  Frontiers in Chemistry  vol. 4, 10.3389/fchem.2016.00034
  • ARSENIYADIS S, Bressy C, Smietana M and Benedetti E (2016). Acetate Biosynthetic Pathway - Polyketides. From Biosynthesis to Total Synthesis Strategies and Tactics For Natural Products  John Wiley & Sons 
  • Amirbekyan K, Duchemin N, Benedetti E, Joseph R, Colon A, Markarian SA, Bethge L, Vonhoff S, Klussmann S, Cossy J, Vasseur J-J, Arseniyadis S and Smietana M (2016). Design, Synthesis, and Binding Affinity Evaluation of Hoechst 33258 Derivatives for the Development of Sequence-Specific DNA-Based Asymmetric Catalysts. American Chemical Society  Acs Catalysis  3096-3105. 10.1021/acscatal.6b00495
  • Schaefers F, Gulder TAM, Bressy C, Smietana M, Benedetti E, Arseniyadis S, Kalesse M and Cordes M (2016). Polyketides. From Biosynthesis to Total Synthesis: Strategies and Tactics For Natural Products  10.1002/9781118754085.ch2

2015

  • Bezagu M, Arseniyadis S, Cossy J, Couture O, Tanter M, Monti F and Tabeling P (2015). A fast and switchable microfluidic mixer based on ultrasound-induced vaporization of perfluorocarbon. Lab On a Chip  vol. 15, (9) 2025-2029. 10.1039/c5lc00247h
  • Benedetti E, Duchemin N, Bethge L, Vonhoff S, Klussmann S, Vasseur JJ, Cossy J, Smietana M and Arseniyadis S (2015). DNA-cellulose: An economical, fully recyclable and highly effective chiral biomaterial for asymmetric catalysis. Chemical Communications  vol. 51, (28) 6076-6079. 10.1039/c4cc10190a

2014

  • Barbeyron R, Benedetti E, Cossy J, Vasseur J, Arseniyadis S and Smietana M (2014). ChemInform Abstract: Recent Developments in Alkyne Borylations. Cheminform  vol. 46, (2) no-no. 10.1002/chin.201502235
  • Barbeyron R, Benedetti E, Cossy J, Vasseur JJ, Arseniyadis S and Smietana M (2014). Recent developments in alkyne borylations. Tetrahedron  vol. 70, (45) 8431-8452. 10.1016/j.tet.2014.06.026
  • Arseniyadis S (2014). Stereoselective Organocatalysis. Bond Formation Methodologies and Activation Modes. Herausgegeben von Ramon Rios Torres. Angewandte Chemie  vol. 126, (43) 11596-11596. 10.1002/ange.201408884
  • Arseniyadis S (2014). Stereoselective Organocatalysis. Bond Formation Methodologies and Activation Modes. Edited by Ramon Rios Torres. Angewandte Chemie International Edition  vol. 53, (43) 11412-11412. 10.1002/anie.201408884
  • Arseniyadis S (2014). Young Career Focus: Dr. Stellios Arseniyadis (ESPCI ParisTech, Paris, France). Synthesis-Stuttgart  vol. 46, (17) A122-A124.
  • Bezagu M, Errico C, Chaulot-Talmon V, Monti F, Tanter M, Tabeling P, Cossy J, Arseniyadis S and Couture O (2014). High spatiotemporal control of spontaneous reactions using ultrasound-triggered composite droplets. Journal of The American Chemical Society  vol. 136, (20) 7205-7208. 10.1021/ja5019354
  • Kolleth A, Cattoen M, Arseniyadis S and Cossy J (2014). ChemInform Abstract: Non‐enzymatic Acylative Kinetic Resolution of Primary Allylic Amines. Cheminform  vol. 45, (7) no-no. 10.1002/chin.201407020
  • Arseniyadis S, Fournier J, Thangavelu S, Lozano O, Prevost S, Archambeau A, Menozzi C and Cossy J (2014). ChemInform Abstract: Palladium‐Catalyzed Allylic Alkylation of Allyl Dienol Carbonates: Reactivity, Regioselectivity, Enantioselectivity, and Synthetic Applications. Cheminform  vol. 45, (4) no-no. 10.1002/chin.201404235

2013

  • ARSENIYADIS S and Spivey AC (2013). Regio- and Position Selective Reactions and Desymmetrizations. Comprehensive Enantioselective Organocatalysis Catalysts, Reactions, and Applications, 3 Volume Set  Wiley-Vch  10.1002/9783527658862.ch41
  • Marrouni AE, Kolleth A, Lebeuf R, Gebauer J, Prevost S, Heras M, Arseniyadis S and Cossy J (2013). ChemInform Abstract: Lyngbouilloside and Related Macrolides from Marine Cyanobacteria. Cheminform  vol. 44, (49) no-no. 10.1002/chin.201349234
  • Wang J, Benedetti E, Bethge L, Vonhoff S, Klussmann S, Vasseur JJ, Cossy J, Smietana M and Arseniyadis S (2013). DNA vs. mirror-image DNA: A universal approach to tune the absolute configuration in DNA-based asymmetric catalysis. Angewandte Chemie - International Edition  vol. 52, (44) 11546-11549. 10.1002/anie.201306232
  • Wang J, Benedetti E, Bethge L, Vonhoff S, Klussmann S, Vasseur J, Cossy J, Smietana M and Arseniyadis S (2013). DNA vs. Mirror‐Image DNA: A Universal Approach to Tune the Absolute Configuration in DNA‐Based Asymmetric Catalysis. Angewandte Chemie  vol. 125, (44) 11760-11763. 10.1002/ange.201306232
  • Arseniyadis S, Fournier J, Thangavelu S, Lozano O, Prevost S, Archambeau A, Menozzi C and Cossy J (2013). Palladium-catalyzed allylic alkylation of allyl dienol carbonates: Reactivity, regioselectivity, enantioselectivity, and synthetic applications. Synlett  vol. 24, (18) 2350-2364. 10.1055/s-0033-1338987
  • Kolleth A, Cattoen M, Arseniyadis S and Cossy J (2013). Non-enzymatic acylative kinetic resolution of primary allylic amines. Chemical Communications  vol. 49, (81) 9338-9340. 10.1039/c3cc45453c
  • Smietana M, Vasseur J, Cossy J and Arseniyadis S (2013). ChemInform Abstract: DNA as a Tool for Molecular Discovery. Cheminform  vol. 44, (30) no-no. 10.1002/chin.201330243
  • ElMarrouni A, Kolleth A, Lebeuf R, Gebauer J, Prevost S, Heras M, Arseniyadis S and Cossy J (2013). Lyngbouilloside and related macrolides from marine cyanobacteria. Natural Product Communications  vol. 8, (7) 965-972. 10.1177/1934578x1300800723
  • Fournier J, Lozano O, Menozzi C, Arseniyadis S and Cossy J (2013). ChemInform Abstract: Palladium‐Catalyzed Asymmetric Allylic Alkylation of Cyclic Dienol Carbonates: Efficient Route to Enantioenriched γ‐Butenolides Bearing an All‐Carbon α‐Quaternary Stereogenic Center. Cheminform  vol. 44, (22) no-no. 10.1002/chin.201322104
  • Colon A, Hoffman TJ, Gebauer J, Dash J, Rigby JH, Arseniyadis S and Cossy J (2013). ChemInform Abstract: Catalysis‐Based Enantioselective Total Synthesis of Myxothiazole Z, (14S)‐Melithiazole G and (14S)‐Cystothiazole F. Cheminform  vol. 44, (10) no-no. 10.1002/chin.201310199
  • Kolleth A, Christoph S, Arseniyadis S and Cossy J (2013). ChemInform Abstract: Kinetic Resolution of Propargylamines via a Highly Enantioselective Non‐enzymatic N‐Acylation Process. Cheminform  vol. 44, (9) no-no. 10.1002/chin.201309022
  • Fournier J, Lozano O, Menozzi C, Arseniyadis S and Cossy J (2013). Palladium-catalyzed asymmetric allylic alkylation of cyclic dienol carbonates: Efficient route to enantioenriched γ-butenolides bearing an all-carbon α-quaternary stereogenic center. Angewandte Chemie - International Edition  vol. 52, (4) 1257-1261. 10.1002/anie.201206368
  • Fournier J, Arseniyadis S and Cossy J (2013). ChemInform Abstract: A Modular and Scalable One‐Pot Synthesis of Polysubstituted Furans. Cheminform  vol. 44, (1) no-no. 10.1002/chin.201301097

2012

  • Fournier J, Lozano O, Menozzi C, Arseniyadis S and Cossy J (2012). Palladium‐Catalyzed Asymmetric Allylic Alkylation of Cyclic Dienol Carbonates: Efficient Route to Enantioenriched γ‐Butenolides Bearing an All‐Carbon α‐Quaternary Stereogenic Center. Angewandte Chemie  vol. 125, (4) 1295-1299. 10.1002/ange.201206368
  • ARSENIYADIS S, Cossy J, Smietana M and Vasseur J-J (2012). DNA as a Tool for Molecular Discovery. Modern Tools For The Synthesis of Complex Bioactive Molecules  John Wiley & Sons  10.1002/9781118342886.ch16
  • Kolleth A, Christoph S, Arseniyadis S and Cossy J (2012). Kinetic resolution of propargylamines via a highly enantioselective non-enzymatic N-acylation process. Chemical Communications  vol. 48, (85) 10511-10513. 10.1039/c2cc35719d
  • Colon A, Hoffman TJ, Gebauer J, Dash J, Rigby JH, Arseniyadis S and Cossy J (2012). Catalysis-based enantioselective total synthesis of myxothiazole Z, (14S)-melithiazole G and (14S)-cystothiazole F. Chemical Communications  vol. 48, (85) 10508-10510. 10.1039/c2cc35721f
  • Cossy J and Arseniyadis S (2012). Modern Tools for the Synthesis of Complex Bioactive Molecules. 10.1002/9781118342886
  • Cossy J and Arseniyadis S (2012). Preface. 10.1002/9781118342886
  • Fournier J, Arseniyadis S and Cossy J (2012). A modular and scalable one-pot synthesis of polysubstituted furans. Angewandte Chemie - International Edition  vol. 51, (30) 7562-7566. 10.1002/anie.201202486
  • Fournier J, Arseniyadis S and Cossy J (2012). A Modular and Scalable One‐Pot Synthesis of Polysubstituted Furans. Angewandte Chemie  vol. 124, (30) 7680-7684. 10.1002/ange.201202486
  • Elmarrouni A, Lebeuf R, Gebauer J, Heras M, Arseniyadis S and Cossy J (2012). Total synthesis of nominal lyngbouilloside aglycon. Organic Letters  vol. 14, (1) 314-317. 10.1021/ol203064r

2011

  • Arseniyadis S, Mahesh M, McDaid P, Hampel T, Davey SG and Spivey AC (2011). Studies towards the N-Acylative kinetic resolution of NOBIN. Collection of Czechoslovak Chemical Communications  vol. 76, (10) 1239-1253. 10.1135/cccc2011034
  • Spivey AC and Arseniyadis S (2011). ChemInform Abstract: Amine, Alcohol and Phosphine Catalysts for Acyl Transfer Reactions. Cheminform  vol. 42, (23) no-no. 10.1002/chin.201123229
  • Dash J, Melillo B, Arseniyadis S and Cossy J (2011). A concise approach towards the synthesis of WS75624 a and WS75624 B via the cross-metathesis of vinyl-functionalized thiazoles. Tetrahedron Letters  vol. 52, (17) 2246-2249. 10.1016/j.tetlet.2011.01.027

2010

  • Elmarrouni A, Fukuda A, Heras M, Arseniyadis S and Cossy J (2010). Expedient synthesis of a stereoisomer of acremolide B. Journal of Organic Chemistry  vol. 75, (24) 8478-8486. 10.1021/jo1017487
  • Elmarrouni A, Joolakanti SR, Colon A, Heras M, Arseniyadis S and Cossy J (2010). Two concise total syntheses of (-)-bitungolide F. Organic Letters  vol. 12, (18) 4074-4077. 10.1021/ol101659y
  • Nicolaou KC, Ortiz A, Zhang H, Dagneau P, Lanver A, Jennings MP, Arseniyadis S, Faraoni R and Lizos DE (2010). ChemInform Abstract: Total Synthesis and Structural Revision of Vannusals A and B: Synthesis of the Originally Assigned Structure of Vannusal B. Cheminform  vol. 41, (37) no-no. 10.1002/chin.201037181
  • Hoffman TJ, Kolleth A, Rigby JH, Arseniyadis S and Cossy J (2010). Stereoselective synthesis of the C1-C11 and C12-C34 fragments of mycalolide A. Organic Letters  vol. 12, (15) 3348-3351. 10.1021/ol101145t
  • Cossy J, Arseniyadis S and Meyer C (2010). Metathesis in Natural Product Synthesis: Strategies, Substrates and Catalysts. 10.1002/9783527629626
  • Cossy J, Arseniyadis S and Meyer C (2010). Preface. 10.1002/9783527629626
  • Nicolaou KC, Ortiz A, Zhang H, Dagneau P, Lanver A, Jennings MP, Arseniyadis S, Faraoni R and Lizos DE (2010). Total synthesis and structural revision of vannusals A and B: Synthesis of the originally assigned structure of vannusal B. Journal of The American Chemical Society  vol. 132, (20) 7138-7152. 10.1021/ja100740t
  • ARSENIYADIS S and Spivey AC (2010). Amine, Alcohol & Phosphine Catalysts for Acyl Transfer Reactions. Asymmetric Organocatalysis  Springer Science & Business Media  10.1007/978-3-642-02815-1_25

2009

  • Hoffman TJ, Dash J, Rigby JH, Arseniyadis S and Cossy J (2009). ChemInform Abstract: Enantioselective Organocatalytic Conjugate Reduction of β‐Azole‐Containing α,β‐Unsaturated Aldehydes. Cheminform  vol. 40, (46) 10.1002/chin.200946133
  • Lebeuf R, Férézou I, Rossier J, Arseniyadis S and Cossy J (2009). Straightforward synthesis of the near-Infrared fluorescent voltagesensitive dye RH1691 and analogues thereof. Organic Letters  vol. 11, (21) 4822-4825. 10.1021/ol901846g
  • Bressy C, Bargiggia F, Guyonnet M, Arseniyadis S and Cossy J (2009). ChemInform Abstract: One‐Pot Hydrosilylation—RCM—Protodesilylation: Application to the Synthesis of ω‐Alkenyl α,β‐Unsaturated Lactones. Cheminform  vol. 40, (29) 10.1002/chin.200929133
  • Hoffman TJ, Dash J, Rlgby JH, Arseniyadis S and Cossy J (2009). Enantioselective organocatalytic conjugate reduction of β-AzoleContaining α,β-unsaturated aldehydes. Organic Letters  vol. 11, (13) 2756-2759. 10.1021/ol900893e
  • Sonawane RP, Joolakanti SR, Arseniyadis S and Cossy J (2009). ChemInform Abstract: Asymmetric Pentenylation of Aldehydes: A New Benchmark for the Preparation of Ethyl‐Substituted Homoallylic Alcohol. Cheminform  vol. 40, (22) 10.1002/chin.200922076
  • Bressy C, Bargiggia F, Guyonnet M, Arseniyadis S and Cossy J (2009). One-pot hydrosilylation-RCM-protodesilylation: Application to the synthesis of ω-alkenyl α,β-unsaturated lactones. Synlett  (4) 565-568. 10.1055/s-0028-1087910
  • Moise J, Sonawane RP, Corsi C, Wendeborn SV, Arseniyadis S and Cossy J (2009). ChemInform Abstract: Formal Synthesis of Leustroducsin B. Cheminform  vol. 40, (8) 10.1002/chin.200908208
  • Sonawane RP, Joolakanti SR, Arseniyadis S and Cossy J (2009). Asymmetric pentenylation of aldehydes: A new benchmark for the preparation of ethyl-substituted homoallylic alcohol. Synlett  (2) 213-216. 10.1055/s-0028-1087641

2008

  • Bressy C, Vors JP, Hillebrand S, Arseniyadis S and Cossy J (2008). Asymmetric total synthesis of the immunosuppressant (-)-pironetin. Angewandte Chemie - International Edition  vol. 47, (52) 10137-10140. 10.1002/anie.200802423
  • Bressy C, Vors J, Hillebrand S, Arseniyadis S and Cossy J (2008). Asymmetric Total Synthesis of the Immunosuppressant (−)‐Pironetin. Angewandte Chemie  vol. 120, (52) 10291-10294. 10.1002/ange.200802423
  • Moïse J, Sonawane RP, Corsi C, Wendeborn SV, Arseniyadis S and Cossy J (2008). Formal synthesis of Leustroducsin B. Synlett  (17) 2617-2620. 10.1055/s-0028-1083511
  • Gebauer J, Arseniyadis S and Cossy J (2008). ChemInform Abstract: Total Synthesis of Cystothiazole A by Microwave‐Assisted Olefin Cross‐Metathesis. Cheminform  vol. 39, (40) 10.1002/chin.200840206
  • Hoffman TJ, Rigby JH, Arseniyadis S and Cossy J (2008). ChemInform Abstract: Synthesis of Vinyl‐Functionalized Oxazoles by Olefin Cross‐Metathesis. Cheminform  vol. 39, (30) 10.1002/chin.200830125
  • Hoffman TJ, Rigby JH, Arseniyadis S and Cossy J (2008). Synthesis of vinyl-functionalized oxazoles by olefin cross-metathesis. Journal of Organic Chemistry  vol. 73, (6) 2400-2403. 10.1021/jo702305g
  • Gebauer J, Arseniyadis S and Cossy J (2008). Facile synthesis of the C1-C13 fragment of lyngbouilloside. Synlett  (5) 712-714. 10.1055/s-2008-1042805
  • Gebauer J, Arseniyadis S and Cossy J (2008). Facile Synthesis of the C1-C13 Fragment of Lyngbouilloside. Synlett  vol. 2008, (05) e1-e1. 10.1055/s-2008-1032212
  • Sabot C, Subhash PV, Valleix A, Arseniyadis S and Mioskowski C (2008). Nonenzymatic kinetic resolution of amines in ionic liquids. Synlett  (2) 268-272. 10.1055/s-2007-1000879
  • Gebauer J, Arseniyadis S and Cossy J (2008). Total synthesis of cystothiazole A by microwave-assisted olefin cross-metathesis. European Journal of Organic Chemistry  (16) 2701-2704. 10.1002/ejoc.200800203
  • Gebauer J, Arseniyadis S and Cossy J (2008). ChemInform Abstract: A Concise Total Synthesis of Melithiazole C. Cheminform  vol. 39, (1) 10.1002/chin.200801209

2007

  • Moise J, Arseniyadis S and Cossy J (2007). Cross‐Metathesis Between α‐Methylene‐γ‐butyrolactone and Olefins: A Dramatic Additive Effect. Cheminform  vol. 38, (36) 10.1002/chin.200736091
  • Gebauer J, Arseniyadis S and Cossy J (2007). A concise total synthesis of melithiazole C+. Organic Letters  vol. 9, (17) 3425-3427. 10.1021/ol701459j
  • Altmann K, Pfeiffer B, Arseniyadis S, Pratt BA and Nicolaou KC (2007). The Chemistry and Biology of Epothilones — The Wheel Keeps Turning. Cheminform  vol. 38, (28) 10.1002/chin.200728239
  • Dash J, Arseniyadis S and Cossy J (2007). Synthesis of Vinyl‐Functionalized Thiazoles by Cross‐Metathesis and Tandem Stille Coupling/Cross‐Metathesis. Cheminform  vol. 38, (18) 10.1002/chin.200718127
  • Moïse J, Arseniyadis S and Cossy J (2007). Cross-metathesis between α-methylene-γ-butyrolactone and olefins: A dramatic additive effect. Organic Letters  vol. 9, (9) 1695-1698. 10.1021/ol0703940
  • Altmann KH, Pfeiffer B, Arseniyadis S, Pratt BA and Nicolaou KC (2007). The chemistry and biology of epothilones - The wheel keeps turning. Chemmedchem  vol. 2, (4) 396-423. 10.1002/cmdc.200600206
  • Dash J, Arseniyadis S and Cossy J (2007). Synthesis of vinyl-functionalized thiazoles by cross-metathesis and tandem stille coupling/cross-metathesis. Advanced Synthesis and Catalysis  vol. 349, (1-2) 152-156. 10.1002/adsc.200600509

2006

  • Nicolaou KC, Pratt BA, Arseniyadis S#37101#, Wartmann M, O'Brate A and Giannakakou P (2006). Molecular Design and Chemical Synthesis of a Highly Potent Epothilone. Cheminform  vol. 37, (22) 10.1002/chin.200622208
  • Nicolaou KC, Pratt BA, Arseniyadis S#37101#, Wartmann M, O'Brate A and Giannakakou P (2006). Cover Picture: Molecular Design and Chemical Synthesis of a Highly Potent Epothilone (ChemMedChem 1/2006). Chemmedchem  vol. 1, (1) 1-1. 10.1002/cmdc.200690000
  • Spivey AC, Arseniyadis S, Fekner T, Maddaford A and Leese DP (2006). Rapid, room-temperature acylative kinetic resolution of sec-alcohols using atropisomeric 4-aminopyridine/triphenylphosphine catalysis. Tetrahedron  vol. 62, (2-3) 295-301. 10.1016/j.tet.2005.08.124
  • Nicolaou KC, Pratt BA, Arseniyadis S#37101#, Wartmann M, O'Brate A and Giannakakou P (2006). Molecular design and chemical synthesis of a highly potent epothilone. Chemmedchem  vol. 1, (1) 41-44. 10.1002/cmdc.200500056

2005

  • Arseniyadis S, Subhash PV, Valleix A, Wagner A and Mioskowski C (2005). Unprecedented, Fully Recyclable, Solid‐Supported Reagent for the Kinetic Resolution of Racemic Amines Through Enantioselective N‐Acetylation. Cheminform  vol. 36, (45) 10.1002/chin.200545087
  • Arseniyadis S, Subhash PV, Valleix A, Wagner A and Mioskowski C (2005). Unprecedented, fully recyclable, solid-supported reagent for the kinetic resolution of racemic amines through enantioselective N-acetylation. Chemical Communications  (26) 3310-3312. 10.1039/b504200c
  • Arseniyadis S, Subhash PV, Valleix A, Mathew SP, Blackmond DG, Wagner A and Mioskowski C (2005). Tuning the enantioselective N-acetylation of racemic amines: A spectacular salt effect. Journal of The American Chemical Society  vol. 127, (17) 6138-6139. 10.1021/ja051302+
  • Spivey AC and Arseniyadis S (2005). Nucleophilic Catalysis by 4‐(Dialkylamino)pyridines Revisited — The Search for Optimal Reactivity and Selectivity. Cheminform  vol. 36, (2) 10.1002/chin.200502244

2004

  • Spivey AC and Arseniyadis S (2004). Nucleophilic catalysis by 4-(dialkylamino)pyridines revisited--the search for optimal reactivity and selectivity. Angew Chem Int Ed Engl  vol. 43, (41) 5436-5441. 10.1002/anie.200460373
  • Arseniyadis S, Valleix A, Wagner A and Mioskowski C (2004). Kinetic resolution of amines: a highly enantioselective and chemoselective acetylating agent with a unique solvent-induced reversal of stereoselectivity. Angew Chem Int Ed Engl  vol. 43, (25) 3314-3317. 10.1002/anie.200453956
  • Arseniyadis S, Wagner A and Mioskowski C (2004). Resin-bound 4-phenyl-1,2-dihydroquinoline (DHQ): a new safety-catch linker for solid-phase organic synthesis (SPOS). Tetrahedron Letters  vol. 45, (10) 2251-2253. 10.1016/j.tetlet.2003.12.161

2002

1995

  • Arseniyadis S and Bressy C (1995). 2,6‐Bis[(4S)‐4,5‐dihydro‐4‐(1‐methylethyl)‐5,5‐diphenyl‐2‐oxazolyl]pyridine. Encyclopedia of Reagents For Organic Synthesis  10.1002/047084289x.rn01405
  • Arseniyadis S and Bressy C (1995). N‐[(1S)‐1‐(Hydroxydiphenylmethyl)‐3‐methylbutyl]‐2‐pyrrolidinecarboxamide. Encyclopedia of Reagents For Organic Synthesis  10.1002/047084289x.rn01406