Advanced search
Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 36, 2006 - Issue 21
Submit an article Journal homepage
154
Views
5
CrossRef citations to date
0
Altmetric
Original Articles

Mild and Efficient Solvent‐Free Friedel–Crafts Acylation of Reserpine

Sabira Begum H.E.J. Research Institute of Chemistry, International Center for Chemical Sciences, University of Karachi, Karachi, PakistanCorrespondence[email protected]
,
Syeda Qamar Zehra H.E.J. Research Institute of Chemistry, International Center for Chemical Sciences, University of Karachi, Karachi, Pakistan
&
Bina S. Siddiqui H.E.J. Research Institute of Chemistry, International Center for Chemical Sciences, University of Karachi, Karachi, Pakistan
Pages 3203-3224 | Received 10 Apr 2006, Published online: 24 Nov 2006
 
Sample our Physical Sciences journals, sign in here to start your FREE access for 14 days

Abstract

The first mild, efficient, solvent‐free Friedel–Crafts acylation of reserpine has been developed, which resulted in the synthesis of 10‐ and 12‐acylated homologues in high overall yields.

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.