4.8 Article

Ruthenium-Catalyzed Alkene-Alkyne Coupling of Disubstituted Olefins: Application to the Stereoselective Synthesis of Trisubstituted Enecarbamates

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 137, Issue 2, Pages 620-623

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja511911b

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Funding

  1. NSF [NSF CHE-1360634]
  2. Direct For Mathematical & Physical Scien
  3. Division Of Chemistry [1360634] Funding Source: National Science Foundation

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The Ru-catalyzed alkene-alkyne coupling reaction has been demonstrated to be an enabling methodology for the synthesis of complex molecules. However, to date, it has been limited to monosubstituted olefins. Herein we report the first general utilization of disubstituted olefins in the Ru-catalyzed alkene-alkyne coupling reaction by employing carbamate directing groups. The products are stereodefined trisusbstituted enecarbamates. The elaboration of these structures toward the asymmetric synthesis of complex aminocyclopentitols and 1,2-amino alcohols is discussed.

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