Advanced search
Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 31, 2001 - Issue 7
Submit an article Journal homepage
100
Views
17
CrossRef citations to date
0
Altmetric
Original Articles

PALLADIUM-CATALYZED ARYLATION AND ARYLOYLATION OF ORGANOSTANNANES WITH TRIARYLBISMUTH(V) DERIVATIVES

Suk-Ku Kang Department of Chemistry, Sungkyunkwan University, Natural Science Campus, Suwon, 440-746, Korea
,
Hyung-Chul Ryu Department of Chemistry, Sungkyunkwan University, Natural Science Campus, Suwon, 440-746, Korea
&
Sang-Woo Lee Department of Chemistry, Sungkyunkwan University, Natural Science Campus, Suwon, 440-746, Korea
Pages 1027-1034 | Accepted 08 May 2000, Published online: 09 Nov 2006
 
Sample our Physical Sciences journals, sign in here to start your FREE access for 14 days

Abstract

The palladium-catalyzed cross-coupling and carbonylative cross-coupling of pentavalent bismuth(V) derivatives with organostannanes have been achieved in CH3CN at room temperature.

ACKNOWLEDGMENTS

Generous financial support from KOSEF-Center for Molecular Design and Synthesis (CMDS) is gratefully acknowledged.

Log in via your institution

Access through your institution

Log in to Taylor & Francis Online

Restore content access

Restore content access for purchases made as guest
Purchase options * Save for later

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 422.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.