BROWSE

Related Researcher

Author's Photo

Park, Cheol-Min
Synthetic & Medicinal Chemistry Lab
Research Interests
  • Organic synthesis, medicinal chemistry, chemical biology

ITEM VIEW & DOWNLOAD

Stereoselective Synthesis of alpha-Diazo Oxime Ethers and Their Application in the Synthesis of Highly Substituted Pyrroles through a [3+2] Cycloaddition

Cited 41 times inthomson ciCited 33 times inthomson ci
Title
Stereoselective Synthesis of alpha-Diazo Oxime Ethers and Their Application in the Synthesis of Highly Substituted Pyrroles through a [3+2] Cycloaddition
Author
Lourdusamy, EmmanuvelYao, LinPark, Cheol-Min
Keywords
Carbenoids; Cycloaddition; Diazo compounds; Heterocycles
Issue Date
2010-10
Publisher
WILEY-V C H VERLAG GMBH
Citation
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.49, no.43, pp.7963 - 7967
Abstract
The stereoselective diazo transfer reaction with oxime ethers offers an efficient route to the corresponding α-diazo oxime ethers. The utility of these compounds has been demonstrated by the synthesis of highly substituted pyrroles through a [3+2] cycloaddition of α-oximino carbenoids with enamines (see scheme).
URI
Go to Link
DOI
10.1002/anie.201004073
ISSN
1433-7851
Appears in Collections:
PHY_Journal Papers
Files in This Item:
2-s2.0-78349243665.pdf Download

find_unist can give you direct access to the published full text of this article. (UNISTARs only)

Show full item record

qrcode

  • mendeley

    citeulike

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

MENU