Baylis–Hillman Reaction of 1‐Formyl‐β‐carboline: One‐Step Synthesis of the Canthin‐6‐one Framework by an Unprecedented Cascade Cyclization Reaction | Zendy

Singh Virender | Zendy; Hutait Samiran | Zendy; Batra Sanjay | Zendy

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Baylis–Hillman Reaction of 1‐Formyl‐β‐carboline: One‐Step Synthesis of the Canthin‐6‐one Framework by an Unprecedented Cascade Cyclization Reaction

Author(s) -

Singh Virender,

Hutait Samiran,

Batra Sanjay

Publication year - 2009

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.200900962

Subject(s) - chemistry , cascade , cascade reaction , baylis–hillman reaction , stereochemistry , medicinal chemistry , combinatorial chemistry , organic chemistry , adduct , catalysis , chromatography

A one‐step access to the canthin‐6‐one architecture by the Baylis–Hillman reaction of methyl 1‐formyl‐9 H ‐β‐carboline‐3‐carboxylate or 1‐formyl‐9 H ‐β‐carboline involving an unprecedented cascade cyclization reaction is reported. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

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