NDLI: A New Modulated Oxidative Ring Cleavage of α-Nitrocycloalkanones by Oxone®: Synthesis of α,ω-Dicarboxylic Acids and α,ω-Dicarboxylic Acid Monomethyl Esters

Content Provider	Scilit
Author	Ballini, Roberto Curini, Massimo Epifano, Francesco Marcotullio, Maria Carla Rosati, Ornelio
Copyright Year	1998
Description	By the appropriate choice of the reaction conditions $Oxone^{®}$ produces the ring cleavage of α-nitrocycloalkanones affording good yields of α,ω-dicarboxylic acids and α,ω-dicarboxylic acid monomethyl esters, respectively, regardless the ring size and/or the presence of an alkyl group as substituent.
Related Links	http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-1998-5740.pdf
Ending Page	1050
Page Count	2
Starting Page	1049
ISSN	09365214
e-ISSN	14372096
DOI	10.1055/s-1998-5740
Journal	Synlett
Issue Number	10
Volume Number	1998
Language	English
Publisher	Georg Thieme Verlag KG
Publisher Date	1998-10-01
Access Restriction	Open
Subject Keyword	Organic Chemistry Α-nitrocycloalkanones Ω-dicarboxylic Acids Ω-dicarboxylic Acid Monomethyl Esters
Content Type	Text
Resource Type	Article
Subject	Organic Chemistry

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A New Modulated Oxidative Ring Cleavage of α-Nitrocycloalkanones by Oxone®: Synthesis of α,ω-Dicarboxylic Acids and α,ω-Dicarboxylic Acid Monomethyl Esters