Advanced search
Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 34, 2004 - Issue 10
Submit an article Journal homepage
140
Views
6
CrossRef citations to date
0
Altmetric
Original Articles

A Facile Synthesis of Dispiro[oxindole‐cyclohexanone] Pyrroloisoquinoline by Formal 1,3‐Dipolar Cycloaddition Strategy

G. Subramaniyan Department of Organic Chemistry, University of Madras, Guindy Campus, Chennai, 600 025, India
&
R. Raghunathan Department of Organic Chemistry, University of Madras, Guindy Campus, Chennai, 600 025, IndiaCorrespondence[email protected]
Pages 1825-1830 | Received 01 Jan 2004, Published online: 20 Aug 2006
 
Sample our Physical Sciences journals, sign in here to start your FREE access for 14 days

Abstract

The conformationally locked s‐trans enone functionality present in the (E)‐2‐arylidene‐1‐cyclohexanones undergoes regioselective 1,3‐dipolar cycloaddition reaction with azomethine ylides generated by the decarboxylative route from tetrahydroisoquinoline‐3‐carboxylic acid and isatin. The regio and stereochemistry of the title compound was established by spectroscopic techniques.

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.