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Asymmetric Synthesis of Bicyclic Amidines via Rhodium-Catalyzed [2+2+2] Cycloaddition of Carbodiimides

A highly enantioselective rhodium-catalyzed [2+2+2] cycloaddition of terminal alkynes and alkenyl carbodiimides has been developed. This reaction demonstrates the feasibility of olefin insertion into carbodiimide-derived metalacycles and provides a new class of chiral bicyclic amidines as the major...

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Published in:Journal of the American Chemical Society 2008-03, Vol.130 (11), p.3262-3263
Main Authors: Yu, Robert T, Rovis, Tomislav
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Language:English
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cited_by cdi_FETCH-LOGICAL-a507t-865aa710a1e7ebf70fd16f2770fd4fd856c1fbd210821e96d9cd631b764385293
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description A highly enantioselective rhodium-catalyzed [2+2+2] cycloaddition of terminal alkynes and alkenyl carbodiimides has been developed. This reaction demonstrates the feasibility of olefin insertion into carbodiimide-derived metalacycles and provides a new class of chiral bicyclic amidines as the major products. An isonitrile migration process responsible for the formation of the minor cycloadduct can be observed and is highly sensitive to the electronics of alkynyl substrates.
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source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
subjects Alkynes - chemistry
Amidines - chemical synthesis
Amidines - chemistry
Bridged Bicyclo Compounds - chemical synthesis
Bridged Bicyclo Compounds - chemistry
Carbodiimides - chemistry
Catalysis
Cyclization
Ligands
Molecular Structure
Rhodium - chemistry
Stereoisomerism
title Asymmetric Synthesis of Bicyclic Amidines via Rhodium-Catalyzed [2+2+2] Cycloaddition of Carbodiimides
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