Journal article
Competing Diels-Alder reactions of activated nitroethylene derivatives and [3,3]-sigmatropic rearrangements of the cycloadducts
Chemical communications (Cambridge, England), v 2(10), pp 1090-191
21 May 2002
PMID: 12122679
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
Diels-Alder reaction of nitroethylene derivatives with cyclohexa-1,3-diene afforded three pericyclic products some of which could be converted to others via a new [3,3]-sigmatropic rearrangement or via a Claisen rearrangement.
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Details
- Title
- Competing Diels-Alder reactions of activated nitroethylene derivatives and [3,3]-sigmatropic rearrangements of the cycloadducts
- Creators
- Peter A Wade - Drexel UniversityJames K Murray, JrSharmila Shah-Patel - Drexel UniversityHung T Le - Drexel University
- Publication Details
- Chemical communications (Cambridge, England), v 2(10), pp 1090-191
- Publisher
- Royal Society of Chemistry
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- [Retired Faculty]
- Web of Science ID
- WOS:000175509300035
- Scopus ID
- 2-s2.0-0037161886
- Other Identifier
- 991019167893704721
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InCites Highlights
Data related to this publication, from InCites Benchmarking & Analytics tool:
- Web of Science research areas
- Chemistry, Multidisciplinary