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Colon, Aude, Hoffman, Thomas J., Gebauer, Julian, Dash, Jyotirmayee, Rigby, James H., Arseniyadis, Stellios, Cossy, Janine (2012) Catalysis-based enantioselective total synthesis of myxothiazole Z, (14S)-melithiazole G and (14S)-cystothiazole F. Chemical Communications, 48 (85). 10508pp. doi:10.1039/c2cc35721f

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Reference TypeJournal (article/letter/editorial)
TitleCatalysis-based enantioselective total synthesis of myxothiazole Z, (14S)-melithiazole G and (14S)-cystothiazole F
JournalChemical Communications
AuthorsColon, AudeAuthor
Hoffman, Thomas J.Author
Gebauer, JulianAuthor
Dash, JyotirmayeeAuthor
Rigby, James H.Author
Arseniyadis, StelliosAuthor
Cossy, JanineAuthor
Year2012Volume48
Issue85
PublisherRoyal Society of Chemistry (RSC)
DOIdoi:10.1039/c2cc35721fSearch in ResearchGate
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Mindat Ref. ID8142777Long-form Identifiermindat:1:5:8142777:8
GUID0
Full ReferenceColon, Aude, Hoffman, Thomas J., Gebauer, Julian, Dash, Jyotirmayee, Rigby, James H., Arseniyadis, Stellios, Cossy, Janine (2012) Catalysis-based enantioselective total synthesis of myxothiazole Z, (14S)-melithiazole G and (14S)-cystothiazole F. Chemical Communications, 48 (85). 10508pp. doi:10.1039/c2cc35721f
Plain TextColon, Aude, Hoffman, Thomas J., Gebauer, Julian, Dash, Jyotirmayee, Rigby, James H., Arseniyadis, Stellios, Cossy, Janine (2012) Catalysis-based enantioselective total synthesis of myxothiazole Z, (14S)-melithiazole G and (14S)-cystothiazole F. Chemical Communications, 48 (85). 10508pp. doi:10.1039/c2cc35721f
In(2012) Chemical Communications Vol. 48 (85) Royal Society of Chemistry (RSC)

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Hoffman, Thomas J., Dash, Jyotirmayee, Rigby, James H., Arseniyadis, Stellios, Cossy, Janine (2009) Enantioselective Organocatalytic Conjugate Reduction of β-Azole-Containing α,β-Unsaturated Aldehydes. Organic Letters, 11. 2756-2759 doi:10.1021/ol900893e
Gebauer, Julian, Arseniyadis, Stellios, Cossy, Janine (2007) A Concise Total Synthesis of Melithiazole C†. Organic Letters, 9. 3425-3427 doi:10.1021/ol701459j
ElMarrouni, Abdelatif, Lebeuf, Raphael, Gebauer, Julian, Heras, Montserrat, Arseniyadis, Stellios, Cossy, Janine (2012) Total Synthesis of Nominal Lyngbouilloside Aglycon. Organic Letters, 14. 314-317 doi:10.1021/ol203064r
Hoffman, Thomas J., Kolleth, Amandine, Rigby, James H., Arseniyadis, Stellios, Cossy, Janine (2010) Stereoselective Synthesis of the C1−C11 and C12−C34 Fragments of Mycalolide A. Organic Letters, 12. 3348-3351 doi:10.1021/ol101145t
Kolleth, Amandine, Christoph, Sarah, Arseniyadis, Stellios, Cossy, Janine (2012) Kinetic resolution of propargylamines via a highly enantioselective non-enzymatic N-acylation process. Chemical Communications, 48 (85). 10511pp. doi:10.1039/c2cc35719d
ElMarrouni, Abdelatif, Joolakanti, Shyamsunder R., Colon, Aude, Heras, Montserrat, Arseniyadis, Stellios, Cossy, Janine (2010) Two Concise Total Syntheses of (−)-Bitungolide F. Organic Letters, 12. 4074-4077 doi:10.1021/ol101659y
Kolleth, Amandine, Gebauer, Julian, ElMarrouni, Abdelatif, Lebeuf, Raphael, Prévost, Céline, Brohan, Eric, Arseniyadis, Stellios, Cossy, Janine (2016) Total Synthesis of Putative 11-epi-Lyngbouilloside Aglycon. Frontiers in Chemistry, 4. doi:10.3389/fchem.2016.00034
Kolleth, Amandine, Cattoen, Martin, Arseniyadis, Stellios, Cossy, Janine (2013) Non-enzymatic acylative kinetic resolution of primary allylic amines. Chemical Communications, 49 (81). 9338pp. doi:10.1039/c3cc45453c
Fournier, Jeremy, Arseniyadis, Stellios, Cossy, Janine (2012) A Modular and Scalable One-Pot Synthesis of Polysubstituted Furans. Angewandte Chemie, 124 (30). 7680-7684 doi:10.1002/ange.201202486
Duchemin, Nicolas, Benedetti, Erica, Bethge, Lucas, Vonhoff, Stefan, Klussmann, Sven, Vasseur, Jean-Jacques, Cossy, Janine, Smietana, Michael, Arseniyadis, Stellios (2016) Expanding biohybrid-mediated asymmetric catalysis into the realm of RNA. Chemical Communications, 52 (55). 8604-8607 doi:10.1039/c6cc03540j
Bressy, Cyril, Vors, Jean-Pierre, Hillebrand, Stefan, Arseniyadis, Stellios, Cossy, Janine (2008) Asymmetric Total Synthesis of the Immunosuppressant (−)-Pironetin. Angewandte Chemie, 120 (52). 10291-10294 doi:10.1002/ange.200802423
 
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