Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Vladimir P. Magloire"'
Publikováno v:
Tetrahedron: Asymmetry. 15:3005-3009
Use of solid-supported reagents simplified routine acylation of primary and secondary alcohols because it eliminated traditional purification. Using a parallel synthesizer, eight primary or secondary alcohols reacted with acid chloride in the presenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c443f5c0a43d3eee3a339b559198cab5
https://doi.org/10.1016/j.tetasy.2004.07.048
https://doi.org/10.1016/j.tetasy.2004.07.048
Publikováno v:
Journal of the American Chemical Society. 127(7)
We report the first biocatalytic route to sulfinamides (R-S(O)-NH2), whose sulfur stereocenter makes them important chiral auxiliaries for the asymmetric synthesis of amines. Subtilisin E did not catalyze hydrolysis of N-acetyl or N-butanoyl arylsulf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fcf249a4f31255946ebe05b15103ff1
https://pubmed.ncbi.nlm.nih.gov/15713087
https://pubmed.ncbi.nlm.nih.gov/15713087
Publikováno v:
Journal of the American Chemical Society. 127:6536-6537
Subtilisin Carlsberg-catalyzed hydrolysis of N-chloroacetyl p-toluenesulfinamide favored cleavage of the sulfinamide (S(O)-N) bond with a minor amount ( approximately 25%) of the expected carboxamide (C(O)-N) bond. The sulfinamide hydrolysis was enan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::364e2b2b3b08e9167ec985cf026937ec
https://doi.org/10.1021/ja0506105
https://doi.org/10.1021/ja0506105