Zobrazeno 1 - 6
of 6
pro vyhledávání: '"John M. Motto"'
Autor:
Erin Sheepwash, Adrian L. Schwan, Laura K. Montemayer, John M. Motto, Alexander Greer, Alvaro Castillo
Publikováno v:
Tetrahedron. 67:1002-1010
We present an experimental and computational study of the reaction of aryl substituted benzyl 1-alkynyl sulfides with potassium alkoxide in acetonitrile, which produces 2-aryl 2,3-dihydrothiophenes in poor to good yields. The cyclization is most effi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d32a80da30be423c7259215ac2c7feff
https://doi.org/10.1016/j.tet.2010.11.104
https://doi.org/10.1016/j.tet.2010.11.104
Publikováno v:
Journal of Sulfur Chemistry. 25:29-37
Using established and new 1H NMR data for sulfinate esters and sulfinyl chlorides, the parameters required for predicting position-dependent alkene 1H NMR chemical shifts of vinylic sulfinate esters and vinylic sulfinyl chlorides have been obtained.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4abf5281459a55e00ecb1822fa532f12
https://doi.org/10.1080/17415990410001662383
https://doi.org/10.1080/17415990410001662383
Publikováno v:
Canadian Journal of Chemistry. 81:423-430
Enantiomerically enriched α,β-unsaturated sulfinate esters of ()-cholesterol undergo stereospecific substitutions at sulfur when treated in benzene at 6°C with Grignard reagents. Sulfoxides with ees of 8599.5% are obtained when enantiopure sul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2ce63e8bbd4e49ca5c222cbb3dbe10c
https://doi.org/10.1139/v03-002
https://doi.org/10.1139/v03-002
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 46:613-622
A convenient synthesis of leflunomide and its primary pharmacologically active metabolite A77 1726, each labeled with four 13C atoms has been achieved. Starting from 13C4-ethyl acetoacetate, each step of the synthesis proceeds in 60–82% yield. Anal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85906e098b9f09d8fc365ee48da075ce
https://doi.org/10.1002/jlcr.701
https://doi.org/10.1002/jlcr.701
Publikováno v:
Journal of the American Chemical Society. 125:12676-12677
The electrochemical reduction of benzyl thiocyanate and p-nitrobenzyl thiocyanate was investigated in acetonitrile at an inert electrode. These two compounds reveal a change in the reductive cleavage mechanism, and more interestingly, they show a cle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62fcc7ad70e001f5a1efd2dba89e131f
https://doi.org/10.1021/ja036710x
https://doi.org/10.1021/ja036710x
Publikováno v:
Journal of Labelled Compounds & Radiopharmaceuticals; Jun2003, Vol. 46 Issue 7, p613, 10p