Total synthesis of complex terpenoids employing radical cascade processes.

Abstract:

:Covering: 2011-2017Radical 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 2011-2017) employing C-C bond-forming radical cascade sequences.

journal_name

Nat Prod Rep

journal_title

Natural product reports

authors

Hung K,Hu X,Maimone TJ

doi

10.1039/c7np00065k

subject

Has Abstract

pub_date

2018-02-21 00:00:00

pages

174-202

issue

2

eissn

0265-0568

issn

1460-4752

journal_volume

35

pub_type

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