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Gold-catalyzed rearrangement of O-vinyl oximes for the synthesis of highly substituted pyrroles.

Ngwerume, Simbarashe and Camp, Jason (2011) Gold-catalyzed rearrangement of O-vinyl oximes for the synthesis of highly substituted pyrroles. Chemical Communications, 47 (6). pp. 1857-1859. ISSN 1359-7345

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Abstract

O-Vinyl oximes were synthesized from the reaction of oximes with activated alkynes and subsequently rearranged using gold catalysis to afford highly substituted pyrroles in an efficient and regiocontrolled process. Addnl., pyrroles were formed directly from oximes and activated alkynes in a multifaceted catalysis process. [on SciFinder(R)]

Item Type: Article
Additional Information: Unmapped bibliographic data: PY - 2011/// [EPrints field already has value set] M3 - 10.1039/c0cc04372a [Field not mapped to EPrints] JA - Chem. Commun. (Cambridge, U. K.) [Field not mapped to EPrints]
Uncontrolled Keywords: Vinyl oxime prepn rearrangement gold catalyst, acetylenecarboxylate ketoxime addn
Subjects: Q Science > Q Science (General)
Q Science > QD Chemistry
Schools: School of Applied Sciences
Related URLs:
Depositing User: Sara Taylor
Date Deposited: 13 Nov 2014 16:43
Last Modified: 13 Nov 2014 16:43
URI: http://eprints.hud.ac.uk/id/eprint/22276

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