Ramanujan, V. B and Sreenivasulu, R and Chavali, M and Sai Pavan Kumar, N. S (2017) Stereoselective total synthesis of decarestrictine J. Monatsh Chem, 148. p. 1865. ISSN 1434-4475
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Official URL: http://dx.doi.org/10.1007/s00706-017-1947-3
Abstract
Abstract
Stereoselective total synthesis of decarestrictine J has been accomplished from inexpensive and commercially available starting materials. This concise synthesis utilizes Jacobsen’s hydrolytic kinetic resolution, regioselective ring opening of epoxide, and Yamaguchi macrolactonisation as key steps.
Graphical abstract Keywords Hydroxy acid Jacobsen’s hydrolytic kinetic resolution Yamaguchi macrolactonisation Stereoselective synthesis Decarestrictine
Item Type: | Article |
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Subjects: | AC Rearch Cluster |
Depositing User: | Unnamed user with email techsupport@mosys.org |
Date Deposited: | 03 Nov 2023 05:51 |
Last Modified: | 03 Nov 2023 05:51 |
URI: | https://ir.vignan.ac.in/id/eprint/273 |