Catalytic Enantioselective Synthesis of Tertiary Thiols From 5<i>H</i>‐Thiazol‐4‐ones and Nitroolefins: Bifunctional Ureidopeptide‐Based Brønsted Base Catalysis

Abstract

Alles dran: Die difunktionelle Brønsted-Base 1 mit Ureidopeptid-Gerüst vermittelt die erste direkte katalytische Michael-Reaktion von α-Mercaptocarboxylat-Surrogaten mit Nitroolefinen. Hierbei wird ein vollständig substituiertes Kohlenstoffzentrum in α-Stellung aufgebaut. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.