Journal article
Formation and [3,3]-sigmatropic rearrangement of O-allyl nitronic esters: a new route to gamma,delta-unsaturated nitro compounds
Chemical communications (Cambridge, England), (24), pp 3531-3532
28 Jun 2009
PMID: 19521597
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
O-Allyl nitronic esters that are obtained from tin(IV) catalyzed Diels-Alder reactions undergo thermal rearrangement to gamma,delta-unsaturated nitro compounds.
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Details
- Title
- Formation and [3,3]-sigmatropic rearrangement of O-allyl nitronic esters: a new route to gamma,delta-unsaturated nitro compounds
- Creators
- Peter A Wade - Drexel UniversityAlma Pipic - Drexel UniversityManikandan Santhanaraman - Drexel UniversityHung T Le - Drexel University
- Publication Details
- Chemical communications (Cambridge, England), (24), pp 3531-3532
- Publisher
- Royal Society of Chemistry
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- [Retired Faculty]
- Web of Science ID
- WOS:000266913400005
- Scopus ID
- 2-s2.0-67650588876
- Other Identifier
- 991019168005204721
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Data related to this publication, from InCites Benchmarking & Analytics tool:
- Web of Science research areas
- Chemistry, Multidisciplinary