Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Matthias Scommoda"'
Publikováno v:
Journal of the American Chemical Society. 117:2453-2466
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e99d72667f045019e160c358adc36c95
https://doi.org/10.1021/ja00114a009
https://doi.org/10.1021/ja00114a009
Publikováno v:
Tetrahedron Letters. 35:7361-7364
Thermolysis of the enantiomerically pure allylic sulfoximines 3a,b leads to their partial rearrangement to the isomeric allylic sulfinamides 5a,b and 6a,b, respectively, with complete retention of configuration at the S-atom. Racemization of the ally
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e12916f21688eeca3ef556bc092ad8b8
https://doi.org/10.1016/0040-4039(94)85314-2
https://doi.org/10.1016/0040-4039(94)85314-2
Publikováno v:
ChemInform. 26
Thermolysis of the enantiomerically pure allylic sulfoximines 3a,b leads to their partial rearrangement to the isomeric allylic sulfinamides 5a,b and 6a,b, respectively, with complete retention of configuration at the S-atom. Racemization of the ally
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15a5a9c42b736cc126b349252cf873c4
https://doi.org/10.1002/chin.199510108
https://doi.org/10.1002/chin.199510108
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::445083d1693c897f558b62c606346035
https://doi.org/10.1002/chin.199531075
https://doi.org/10.1002/chin.199531075
Publikováno v:
ChemInform. 27
Enantiomerically pure N-methyl-, N-benzyl-, and N-(methoxyethyl)-S-(phenyl)cinnamylsulfoximines as well as the corresponding crotylsulfoximines have been prepared from N-methyl-, N-benzyl-, and N-(methoxyethyl)-S-(lithiomethyl)sulfoximines and carbon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::188e9d288016d4fad911ac39cd644072
https://doi.org/10.1002/chin.199645051
https://doi.org/10.1002/chin.199645051
Publikováno v:
The Journal of organic chemistry. 61(13)
Enantiomerically pure N-methyl-, N-benzyl-, and N-(methoxyethyl)-S-(phenyl)cinnamylsulfoximines as well as the corresponding crotylsulfoximines have been prepared from N-methyl-, N-benzyl-, and N-(methoxyethyl)-S-(lithiomethyl)sulfoximines and carbon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e65f669002f5a453d1ca4a5175df0f1c
https://pubmed.ncbi.nlm.nih.gov/11667341
https://pubmed.ncbi.nlm.nih.gov/11667341