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Employing α‐Diazocarbonyl Compound Chemistry in the Assembly of Medicinally Important Aryl(alkyl)thiolactam Scaffold
Author(s) -
Barkhatova Darina,
Zhukovsky Daniil,
Dar'in Dmitry,
Krasavin Mikhail
Publication year - 2019
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.201900944
Subject(s) - diazo , chemistry , aryl , alkyl , steric effects , combinatorial chemistry , organic chemistry
RH 2 (OAc) 4 ‐catalyzed coupling of α‐diazo‐γ‐butyrolactams with a wide range of aliphatic and aromatic thiols leads to α‐aryl(alkyl)thiolactams in generally good yields. The transformation was found to be tolerant to sterically hindered thiols in contrast to analogous O–H insertion. Moreover, the same diazo lactams can be easily converted to β‐aryl(alkyl)thiolactams in two steps using one‐pot protocol. Consequently, the continued synthetic exploration of α‐diazo‐γ‐butyrolactams paves the way toward two medicinally important scaffolds.

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