Journal article
Selective reductions of conjugated acetylenes with magnesium in methanol and methanol-D
Tetrahedron letters, v 30(1)
1989
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
The combination of magnesium in methanol or methanol-d offers an efficient, convenient and selective method for reduction of acetylenic bonds conjugated to esters (but not acids) or to two phenyl groups to the saturated or tetradeuterated derivatives, respectively.
The combination of Mg in methanol or methanol-d provides a convenient and effective system for the reduction of acetylenic bonds conjugated to esters or to two phenyl groups to the saturated or tetradeuterated derivatives.
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Details
- Title
- Selective reductions of conjugated acetylenes with magnesium in methanol and methanol-D
- Creators
- Robert O. Hutchins - Drexel UniversitySuchismita - Drexel UniversityRobert E. Zipkin - BIOMOL Research Laboratories, Inc., 5166 Campus Drive, Plymouth Meeting, PA 19462 USAIra M. Taffer - BIOMOL Research Laboratories, Inc., 5166 Campus Drive, Plymouth Meeting, PA 19462 USAR. Sivakumar - BIOMOL Research Laboratories, Inc., 5166 Campus Drive, Plymouth Meeting, PA 19462 USAArthur Monaghan - BIOMOL Research Laboratories, Inc., 5166 Campus Drive, Plymouth Meeting, PA 19462 USAE.Michael Elisseou - BIOMOL Research Laboratories, Inc., 5166 Campus Drive, Plymouth Meeting, PA 19462 USA
- Publication Details
- Tetrahedron letters, v 30(1)
- Publisher
- Elsevier
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- College of Arts and Sciences
- Web of Science ID
- WOS:A1989R911300013
- Scopus ID
- 2-s2.0-0002686380
- Other Identifier
- 991019173893104721
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- Web of Science research areas
- Chemistry, Organic