Document Detail


The Decarboxylative Strecker Reaction.
MedLine Citation:
PMID:  22087753     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
α-Amino acids react with aldehydes in the presence of a cyanide source to form α-amino nitriles in what can be considered a decarboxylative variant of the classical Strecker reaction. This unprecedented transformation does not require the use of a metal catalyst and provides facile access to valuable α-amino nitriles that are inaccessible by traditional Strecker chemistry.
Authors:
Deepankar Das; Matthew T Richers; Longle Ma; Daniel Seidel
Related Documents :
10350493 - Oleate salt formation and mesomorphic behavior in the propranolol/oleic acid binary sys...
19637983 - Chitosan and its salts for mucosal and transmucosal delivery.
16214973 - Enteral formula use in children after small bowel transplant.
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2011-11-16
Journal Detail:
Title:  Organic letters     Volume:  -     ISSN:  1523-7052     ISO Abbreviation:  -     Publication Date:  2011 Nov 
Date Detail:
Created Date:  2011-11-17     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  100890393     Medline TA:  Org Lett     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Affiliation:
Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854, United States.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Fluorescence Dynamics and Dipole Moment Evolution of Singlet Exciton Decay in Conjugated Polymers.
Next Document:  Exposure to repetitive tasks induces motor changes related to skill acquisition and inflammation in ...