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Journal article
Alkenenitrile Transmissive Olefination: Synthesis of the Putative Lignan "Morinol I"
European journal of organic chemistry, v 2011(34), pp 6843-6846
Dec 2011
PMID: 22545004
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Abstract
Grignard reagents trigger an additionelimination with a'-hydroxy acrylonitriles to selectively generate Z-alkenenitriles. The modular assembly of Z-alkenenitriles from a Grignard reagent, acrylonitrile, and an aldehyde is ideal forstereoselectively synthesizing alkenes, as illustrated in the synthesis of the putative lignan morinol I.
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Details
- Title
- Alkenenitrile Transmissive Olefination: Synthesis of the Putative Lignan "Morinol I"
- Creators
- Fraser F. Fleming - Duquesne UniversityWang Liu - The Ohio State UniversityLihua Yao - Duquesne UniversityBhaskar Pitta - Duquesne UniversityMatthew Purzycki - Duquesne UniversityP. C. Ravikumar - Indian Institute of Technology Mandi
- Publication Details
- European journal of organic chemistry, v 2011(34), pp 6843-6846
- Publisher
- Wiley
- Number of pages
- 4
- Grant note
- 2R15AI051352-03 / National Institutes of Health; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA R15AI051352 / NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Allergy & Infectious Diseases (NIAID) 0808996; 0614785; 024872; 0421252 / National Science Foundation; National Science Foundation (NSF)
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- Chemistry
- Web of Science ID
- WOS:000297205800002
- Scopus ID
- 2-s2.0-81855206130
- Other Identifier
- 991020898499704721
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- Collaboration types
- Domestic collaboration
- International collaboration
- Web of Science research areas
- Chemistry, Organic