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The Crucial Role of S ‐oxidation State on the Selectivity and Reaction Rate of the 1,3‐Dipolar Cycloaddition of Azomethine Ylides and Homochiral Thiazolines
Author(s) -
GraciaVitoria Jaime,
Osante Iñaki,
Cativiela Carlos
Publication year - 2021
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.202100237
Subject(s) - chemistry , enantiopure drug , cycloaddition , regioselectivity , selectivity , sulfoxide , azomethine ylide , thiazoline , reactivity (psychology) , thiazolidine , sulfone , sulfur , medicinal chemistry , oxidation state , pyrrolidine , 1,3 dipolar cycloaddition , catalysis , organic chemistry , enantioselective synthesis , medicine , alternative medicine , pathology
The novel enantiopure synthesis of protected proline‐cysteine analogs by means of 1,3‐dipolar cycloaddition of homochiral thiazolines and azomethine ylides is described. The important role of the oxidation state of the sulfur atom of the dipolarophile in such reaction is demonstrated affecting strongly the regioselectivity and reactivity of the 1,3‐dipolar cycloaddition. Mono‐oxidized sulfur atom (sulfoxide group) and di‐oxidized (sulfone group) led to 2,3 regio‐addition whereas reactions starting from non‐oxidized sulfur atom resulted in the 2,4 addition. Besides, sulfur oxidized thiazolines reacted smoothly upon heating in an organic solvent media but the non‐oxidized sulfur thiazoline required metal catalysis. Diastereofacial selectivity was observed to be independent of the oxidation state of the sulfur atom but controlled by the bulky tert ‐butyl group at the thiazoline ring. The highly substituted and functionalized enantiopure pyrrolidine‐thiazolidine bicyclic compounds are considered as novel (homo)cysteine‐proline analogs with important properties to discover.