Merck
CN

Asymmetric bromolactonization using amino-thiocarbamate catalyst.

Journal of the American Chemical Society (2010-10-16)
Ling Zhou, Chong Kiat Tan, Xiaojian Jiang, Feng Chen, Ying-Yeung Yeung
ABSTRACT

A novel amino-thiocarbamate-catalyzed bromolactonization of unsaturated carboxylic acids has been developed. The scope of the reaction is evidenced by 22 examples of γ-lactones with up to 99% yield and 93% ee. The protocol was applied in the enantioselective synthesis of the key intermediates of VLA-4 antagonists.

MATERIALS
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Brand
Product Description

Sigma-Aldrich
Methylboronic acid, 97%