Journal article
Generation and in situ Diels–Alder reactions of activated nitroethylene derivatives
Tetrahedron letters, v 43(14), pp 2585-2588
2002
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
Dienes readily undergo Diels–Alder reaction with CH
2C(NO
2)SO
2Ph (
2a
), CH
2C(NO
2)CO
2Et (
2b
), and CH
2C(NO
2)COPh (
2c
), all observed in situ by
1H NMR. The cycloadducts of
2a
undergo S
RN1 reactions.
Activated nitroethylene derivatives can be easily generated and used in situ for Diels–Alder reactions.
Metrics
Details
- Title
- Generation and in situ Diels–Alder reactions of activated nitroethylene derivatives
- Creators
- Peter A. Wade - Drexel UniversityJames K. Murray - Drexel UniversitySharmila Shah-Patel - Drexel UniversityPatrick J. Carroll - University of Pennsylvania
- Publication Details
- Tetrahedron letters, v 43(14), pp 2585-2588
- Publisher
- Elsevier
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- [Retired Faculty]
- Web of Science ID
- WOS:000174978100024
- Scopus ID
- 2-s2.0-0036532542
- Other Identifier
- 991019167883804721
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- Collaboration types
- Domestic collaboration
- Web of Science research areas
- Chemistry, Organic