A new, modulated, oxidative ring cleavage of alpha-nitrocycloalkanones by Oxone (R): Synthesis of alpha,omega-dicarboxylic acids and alpha,omega-dicarboxylic acid monomethyl esters (pg 1049, 1998)

Authors
Ballini, R Curini, M Epifano, F Marcotullio, MC Rosati, O
Citation
R. Ballini et al., A new, modulated, oxidative ring cleavage of alpha-nitrocycloalkanones by Oxone (R): Synthesis of alpha,omega-dicarboxylic acids and alpha,omega-dicarboxylic acid monomethyl esters (pg 1049, 1998), SYNLETT, (12), 1998, pp. 1461
Citations number
24
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
SYNLETT
ISSN journal
09365214 → ACNP
Issue
12
Year of publication
1998
Database
ISI
SICI code
0936-5214(199812):12<1461:ANMORC>2.0.ZU;2-O
Abstract
By the appropriate choice of the reaction conditions Oxone(R) produces the ring cleavage of alpha-nitrocycloalkanones affording good yields of alpha,o mega-dicarboxylic acids and alpha,omega-dicarboxylic acid monomethyl esters , respectively, regardless of the ring size and/or the presence of an alkyl group as substituent.