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Total synthesis of complex terpenoids employing radical cascade processes.
- Source :
-
Natural Product Reports . Feb2018, Vol. 35 Issue 2, p174-202. 29p. - Publication Year :
- 2018
-
Abstract
- Covering: 2011ā2017 Radical cyclizations have a rich history in organic chemistry and have been particularly generous to the field of natural product synthesis. Owing to their ability to operate in highly congested molecular quarters, and with significant functional group compatibility, these transformations have enabled the synthesis of numerous polycyclic terpenoid natural products over the past several decades. Moreover, when programmed accordingly into a synthetic plan, radical cascade processes can be used to rapidly assemble molecular complexity, much in the same way nature rapidly constructs terpene frameworks through cationic cyclization pathways. This review highlights recent total syntheses of complex terpenoids (from 2011ā2017) employing CāC bond-forming radical cascade sequences. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 02650568
- Volume :
- 35
- Issue :
- 2
- Database :
- Academic Search Index
- Journal :
- Natural Product Reports
- Publication Type :
- Academic Journal
- Accession number :
- 128123801
- Full Text :
- https://doi.org/10.1039/c7np00065k