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Oxidative alkoxycarbonylation of terminal alkenes with carbazates.

A range of terminal alkenes smoothly underwent palladium-catalyzed oxidative alkoxycarbonylation with carbazates under an oxygen atmosphere to afford structurally diverse α,β-unsaturated esters in moderate to good yields with excellent regioselectivity and E selectivity.

Journal Title: Chemical communications (Cambridge England), July 25, 2013, Vol.49(58), pp.6528-6530
Main Author: Su, Yu-Han
Other Authors: Wu, Zhao , Tian, Shi-Kai
Format: Electronic Article Electronic Article
Language: English
Subjects:
ID: E-ISSN: 1364-548X ; DOI: 1364-548X ; DOI: 10.1039/c3cc42994f
Link: http://search.proquest.com/docview/1372080743/?pq-origsite=primo
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recordid: proquest1372080743
title: Oxidative alkoxycarbonylation of terminal alkenes with carbazates.
format: Article
creator:
  • Su, Yu-Han
  • Wu, Zhao
  • Tian, Shi-Kai
subjects:
  • Alkenes–Chemistry
  • Copper–Chemistry
  • Esters–Chemistry
  • Hydrazines–Chemistry
  • Oxidation-Reduction–Chemistry
  • Oxygen–Chemistry
  • Palladium–Chemistry
  • Alkenes
  • Esters
  • Hydrazines
  • Palladium
  • Copper
  • Oxygen
ispartof: Chemical communications (Cambridge, England), July 25, 2013, Vol.49(58), pp.6528-6530
description: A range of terminal alkenes smoothly underwent palladium-catalyzed oxidative alkoxycarbonylation with carbazates under an oxygen atmosphere to afford structurally diverse α,β-unsaturated esters in moderate to good yields with excellent regioselectivity and E selectivity.
language: eng
source:
identifier: E-ISSN: 1364-548X ; DOI: 1364-548X ; DOI: 10.1039/c3cc42994f
fulltext: fulltext
issn:
  • 1364548X
  • 1364-548X
url: Link


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