| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5215512 | Tetrahedron | 2015 | 25 Pages |
Abstract
An enantioconvergent synthesis of the advanced intermediate of macroviracin A has been developed, using enantioselective lipase-catalyzed acylation, asymmetric allylation, and asymmetric dihydroxylation reaction to install the required stereogenic centers. The key reactions proceeded with good to excellent stereoselectivity.
Related Topics
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Chemistry
Organic Chemistry
Authors
Seema V. Kanojia, Sucheta Chatterjee, Sunita Gamre, Subrata Chattopadhyay, Anubha Sharma,