The Baylis–Hillman acetates in organic synthesis: Unprecedented sodium nitrite induced intramolecular Friedel–Crafts cyclization of secondary nitro compounds-Reference-Cited by-同舟云学术

The Baylis–Hillman acetates in organic synthesis: Unprecedented sodium nitrite induced intramolecular Friedel–Crafts cyclization of secondary nitro compounds

Published:2014 Issue:46 Volume:4 Page:23966-23970
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Basavaiah Deevi¹²³,Reddy Daggula Mallikarjuna¹²³

Affiliation:

1. School of Chemistry

2. University of Hyderabad

3. Hyderabad-500 046, India

Abstract

Unprecedented sodium nitrite mediated intramolecular Friedel–Crafts cyclization of alkyl (E)-2-arylidene-4-nitroalkanoates and (E)-3-arylidene-5-nitroalkan-2-ones derived from Baylis–Hillman acetates has been described.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA03573A

Reference64 articles.

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2. Nitro and related groups

3. The Henry reaction: recent examples

4. Nitroalkanes as new, ideal precursors for the synthesis of benzene derivatives

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