Organocatalytic Asymmetric Michael Addition of Rhodanines to Azadienes for Assembling of Sulfur‐containing Tetrasubstituted Carbon Stereocenters
Stereocenter
Rhodanine
Squaramide
Michael reaction
DOI:
10.1002/adsc.201801422
Publication Date:
2018-11-20T03:26:33Z
AUTHORS (6)
ABSTRACT
Abstract The squaramide catalyzed enantioselective Michael addition of rhodanines to 2‐arylidene‐ N ‐tosylbenzofuran‐3(2 H )‐imines has been established, which enables the formation benzofurans bearing both rhodanine and sulfur‐containing tetrasubstituted stereocenter structural motif in good high yields with excellent enantio‐ diastereoselectivities. magnified image
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