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

Andrea Buzas 1 Florin M. Istrate 1 X. F Le Goff 2 yann Odabachian 1 Fabien L. Gagosz 1 
1 DCSO - Laboratoire de synthèse organique
2 DCPH - Laboratoire Hétéroéléments et Coordination
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.
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https://hal-polytechnique.archives-ouvertes.fr/hal-00968361
Contributor : Denis Roura Connect in order to contact the contributor
Submitted on : Monday, March 31, 2014 - 9:18:58 PM
Last modification on : Friday, February 4, 2022 - 9:02:01 AM

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X | CNRS | X-DCSO | X-DCPH | X-DEP-CHIM | INC-CNRS

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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, Elsevier, 2009, 694 (4), pp.515-519. ⟨10.1016/j.jorganchem.2008.11.004⟩. ⟨hal-00968361⟩

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