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Synthesis 2016; 48(24): 4347-4380
DOI: 10.1055/s-0035-1562530
DOI: 10.1055/s-0035-1562530
short review
Recent Advances in the Synthesis and Reactivity of Vinylcyclopropanes
Further Information
Publication History
Received: 11 May 2016
Accepted after revision: 05 July 2016
Publication Date:
09 September 2016 (online)
Abstract
In this review, we present the recent advances in the synthesis and reactivity of vinylcyclopropanes (VCPs). Various important methodologies involving ylides, carbenoid chemistry, metal-mediated cycloaddition reactions, and allylic cyclization methodologies for the synthesis of VCPs are described. Based on the type of VCPs, their reactivity is dealt under electrophile-, radical-, and nucleophile-mediated reactions. Several examples from transition-metal-mediated ring-opening reactions are discussed.
1 Introduction
2 Synthetic Routes to Vinylcyclopropanes
2.1 Ylide Chemistry
2.2 Transition-Metal-Mediated Synthesis
3 Reactivity of Vinylcyclopropanes
3.1 Electrophile-Mediated Ring-Opening Reactions
3.2 Radical-Mediated Ring-Opening Reactions
3.3 Nucleophile-Mediated Ring-Opening Reactions
3.4 Transition-Metal-Mediated Ring-Opening Reactions
4 Conclusion
-
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