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  • Organocatalytic, asymmetric synthesis of 3-sulfenylated N-Boc-protected oxindoles.

Organocatalytic, asymmetric synthesis of 3-sulfenylated N-Boc-protected oxindoles.

Chemistry (Weinheim an der Bergstrasse, Germany) (2012-07-28)
Chuan Wang, Xuena Yang, Charles C J Loh, Gerhard Raabe, Dieter Enders
ABSTRACT

Sulfenylated oxindoles: The first asymmetric sulfenylation of N-Boc-protected oxindoles has been developed to provide products containing a tetrasubstituted stereogenic center in high to excellent yields (86-98 %) and, in most cases, excellent enantioselectivities (up to 96 % ee; see scheme).

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
(S)-(+)-2-Pyrrolidinemethanol, 97%