Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2675
Title: p-Nitrophenyl carbonate promoted ring-opening reactions of DBU and DBN affording lactam carbamates
Authors: VANGALA, MADHURI
Shinde, Ganesh P.
Dept. of Chemistry
Keywords: Carbonates
DBN
DBU
lactams
p-nitrophenyl
Organic bases
2016
Issue Date: Sep-2016
Publisher: Beilstein-Institute
Citation: Beilstein Journal of Organic Chemistry, 12(1), 2086-2092.
Abstract: The amidine bases DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) and DBN (1,5-diazabicyclo[4.3.0]non-5-ene) display nucleophilic behaviour towards highly electrophilic p-nitrophenyl carbonate derivatives with ring opening of the bicyclic ring to form corresponding substituted ε-caprolactam and γ-lactam derived carbamates. This simple method presents a unified strategy to synthesize structurally diverse ε-caprolactam and γ-lactam compounds with a large substrate scope.
URI: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2675
https://doi.org/10.3762/bjoc.12.197
ISSN: 1860-5397
1860-5397
Appears in Collections:JOURNAL ARTICLES

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