Reactions of metallocarbenes derived from N-sulfonyl-1,2,3-triazoles
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Abstract
Metal-stabilized carbenes derived from diazo compounds have become broadly useful reactive intermediates for organic synthesis. This tutorial review will describe the recent advances in using N-sulfonyl-1,2,3-triazoles as precursors for the formation of metal-bound imino carbene intermediates. These intermediates undergo a variety of synthetically useful transformations, which include transannulation reactions to generate new heterocycles, cyclopropanation and subsequent ring expansions, ylide formation with subsequent rearrangements, and C-H functionalization. Furthermore, many of these transformations can be conducted with high levels of enantioselectivity by use of chiral rhodium(II) catalysts.
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600
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Authors
2Topics & keywords
Topics
Keywords
- Carbene
- Diazo
- Sulfonyl
- Cyclopropanation
- Ylide
- Chemistry
- Rhodium
- Catalysis
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