Profiles
Research Units
Publications
Sign Up
Faculty Login
X
Articles
Formation of pentacyclic structures by a domino sequence on cyclic enamides
Satyanarayana Gedu
,
C. Maichle-Mössmer
,
M.E. Maier
Published in Royal Society of Chemistry
2009
DOI:
10.1039/b820636h
Issue: 12
Pages: 1571 - 1573
Abstract
Novel spiropentacyclic compounds 11 were obtained from cyclic enamides of type 9, featuring a (2-bromophenyl)propyl substituent in the 5-position, through a Pd-mediated domino sequence taking place via Heck insertion and C-H activation. © 2009 The Royal Society of Chemistry.
Request full-text
Cite
Content may be subject to copyright.
Journal Details
Authors (1)
About the journal
Journal
Data powered by Typeset
Chemical Communications
Publisher
Data powered by Typeset
Royal Society of Chemistry
ISSN
13597345
Authors (1)
Satyanarayana Gedu
Department of Chemistry
Recent publications
Recyclable Aliphatic Nitrile-Template Enabled Remote meta-C-H Functionalization at Room Temperature
A simple removable aliphatic nitrile template 2-cyano-2,2-di-isobutyl acetic acid for remote meta -selective C-H functionalization
1,2,3,4-Tetrahydroisoquinolines as inhibitors of HIV-1 integrase and human LEDGF/p75 interaction
A Metal-Free Path to 2-Iodo-3-alkyl-1-arylbut-2-en-1-ones and Their Application to the Domino Synthesis of Functionalized 2 H-Pyran-2-ones
Get all the updates for this publication
Follow