Gold(I)-catalyzed [4+2] cycloaddition of N-(hex-5-enynyl) tert-butyloxycarbamates - Archive ouverte HAL Access content directly
Journal Articles Journal of Organometallic Chemistry Year : 2009

Gold(I)-catalyzed [4+2] cycloaddition of N-(hex-5-enynyl) tert-butyloxycarbamates

(1) , (1) , (2) , (1) , (1)
1
2

Abstract

A study concerning the gold(I)-catalyzed transformation of N-(hex-5-enynyl) tert-butyloxycarbamates is described. The mild conditions employed allow the moderately efficient but stereoselective synthesis of a range of bicyclic carbamates following a formal [4+2] cycloaddition process.
Not file

Dates and versions

hal-00968361 , version 1 (31-03-2014)

Identifiers

Cite

Andrea Buzas, Florin M. Istrate, X. F Le Goff, Yann Odabachian, Fabien L. Gagosz. Gold(I)-catalyzed [4+2] cycloaddition of N-(hex-5-enynyl) tert-butyloxycarbamates. Journal of Organometallic Chemistry, 2009, 694 (4), pp.515-519. ⟨10.1016/j.jorganchem.2008.11.004⟩. ⟨hal-00968361⟩
52 View
0 Download

Altmetric

Share

Gmail Facebook Twitter LinkedIn More