| Literature DB >> 20104842 |
Abstract
New reactions of azomethine ylides with nontraditional dipolarophiles are reported. Azomethine ylides, formed in situ via decarboxylative condensations of alpha-amino acids with aldehydes, undergo reactions with naphthols, indoles, alkynes, and nitroalkanes.Entities:
Mesh:
Substances:
Year: 2010 PMID: 20104842 DOI: 10.1021/ja910719x
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419