Publication: Pyrrolidine and α-methylene-α-lactam from the cyclization of α-(alkylaminoethyl)acrylate: Synthesis of aza-sarkomycins
dc.contributor.author | Bonkoch Tarnchompoo | en_US |
dc.contributor.author | Chachanat Thebtaranonth | en_US |
dc.contributor.author | Yodhathai Thebtaranonth | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.date.accessioned | 2018-06-14T09:01:05Z | |
dc.date.available | 2018-06-14T09:01:05Z | |
dc.date.issued | 1987-01-01 | en_US |
dc.description.abstract | Diene 1 readily adds primary amines to give 2 which can cyclize either in a Michael addition fashion or via a displacement reaction to give, respectively, pyrrolidine 3 or methylene lactam 4 which further isomerizes to 5 under the employed reaction conditions. Compound 4 can be obtained as the sole product from the reaction of diene precursor 7 with amines followed by vacuum pyrolysis. © 1987. | en_US |
dc.identifier.citation | Tetrahedron Letters. Vol.28, No.52 (1987), 6675-6678 | en_US |
dc.identifier.doi | 10.1016/S0040-4039(00)96943-0 | en_US |
dc.identifier.issn | 00404039 | en_US |
dc.identifier.other | 2-s2.0-0023579210 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/15321 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0023579210&origin=inward | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | Pyrrolidine and α-methylene-α-lactam from the cyclization of α-(alkylaminoethyl)acrylate: Synthesis of aza-sarkomycins | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0023579210&origin=inward | en_US |