Total Synthesis of Bryostatin8 Using an Organosilane-Based Strategy
Convergent total synthesis of bryostatin8 has been accomplished by an organosilane-based strategy. The Cring is constructed stereoselectively through a geminal bis(silane)-based [1,5]-Brook rearrangement, and the Bring through geminal bis(silane)-based Prins cyclization, thus efficiently joining the...
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Published in | Angewandte Chemie International Edition Vol. 57; no. 4; p. 942 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
Wiley Subscription Services, Inc
22.01.2018
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Edition | International ed. in English |
Subjects | |
Online Access | Get full text |
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Summary: | Convergent total synthesis of bryostatin8 has been accomplished by an organosilane-based strategy. The Cring is constructed stereoselectively through a geminal bis(silane)-based [1,5]-Brook rearrangement, and the Bring through geminal bis(silane)-based Prins cyclization, thus efficiently joining the northern and southern parts of the molecule. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.201711452 |