Bromo–nitro substitution on a tertiary α carbon—a previously uncharacterized facet of the Kornblum substitution-Reference-Cited by-同舟云学术

Bromo–nitro substitution on a tertiary α carbon—a previously uncharacterized facet of the Kornblum substitution

Published:2015 Issue:93 Volume:5 Page:76401-76418
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Leonard Matthew J.¹²³,McKay Peter G.¹²³,Lingham Anthony R.¹²³

Affiliation:

1. RMIT University

2. Melbourne 3001

3. Australia

Abstract

Sodium nitrite in dimethylformamide substitutes nitro for bromine alpha to an amide carbonyl in high yield at a tertiary site.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA14798K

Reference105 articles.

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3. A New Synthesis of α-Nitroesters1,2

4. N. Ono , The nitro group in organic synthesis, Wiley publishing, 1991

5. N. Ono , The nitro group in organic synthesis, Wiley publishing, ISBNs: 0-471-31611-3 (Hardback); 0-471-22448-0 (Electronic), 2001

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