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)]

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URI:

https://eprints.hud.ac.uk/id/eprint/22276

URI:

https://eprints.hud.ac.uk/id/eprint/22276

URI:

https://eprints.hud.ac.uk/id/eprint/22276

URI:

https://eprints.hud.ac.uk/id/eprint/22276

URI:

https://eprints.hud.ac.uk/id/eprint/22276

URI:

https://eprints.hud.ac.uk/id/eprint/22276

URI:

https://eprints.hud.ac.uk/id/eprint/22276

URI:

https://eprints.hud.ac.uk/id/eprint/22276

URI:

https://eprints.hud.ac.uk/id/eprint/22276

URI:

https://eprints.hud.ac.uk/id/eprint/22276

Title:

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

Creators:

Ngwerume, Simbarashe and Camp, Jason

Identification Number:

10.1039/c0cc04372a

Official URL:

http://dx.doi.org/10.1039/c0cc04372a

Date:

January 2011

Subjects:

Q Science > Q Science (General)
Q Science > QD Chemistry

Schools:

School of Applied Sciences

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

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Item Type:

Article

Depositing User:

Sara Taylor

Date Deposited:

13 Nov 2014 16:43

Revision:

Last Modified:

28 Aug 2021 11:43