Transannulation Reactions in the Synthesis of Natural Products - Research Database, The University of York

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Transannulation Reactions in the Synthesis of Natural Products

Research output: Contribution to journal › Literature review › peer-review

Published copy (DOI)

10.1055/s-0028-1083355

Author(s)

Paul A. Clarke
Andrew T. Reeder
Joby Winn

Department/unit(s)

Chemistry

Publication details

Journal	SYNTHESIS-STUTTGART
Date	Published - 2 Mar 2009
Issue number	5
Number of pages	19
Pages (from-to)	691-709
Original language	English

Abstract

An overview on the construction of polycyclic natural products by use of transannulation reactions across medium and large rings is presented.

Research areas

transannulation, polycyclic, natural products, ASYMMETRIC TOTAL-SYNTHESIS, TRANS-ANNULAR CYCLIZATION, FORMAL TOTAL-SYNTHESIS, DIELS-ALDER REACTIONS, DEF-RING CORE, ENANTIOSELECTIVE SYNTHESIS, RADICAL CYCLIZATIONS, HEXACYCLINIC ACID, STRATEGY, CASCADE

Research outputs

Studies on transannulation reactions across a nine-membered ring: the synthesis of natural product-like structures
Research output: Contribution to journal › Article › peer-review

Projects

Novel Transannulation Strategies for the Synthesis of Polycyclic Sesquiterpenoid Natural Products
Project: Research project (funded) › Research

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