Zobrazeno 1 - 10
of 27
pro vyhledávání: '"N. M. Mollov"'
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1afef5e936334d3d283e4e3043027ea2
https://doi.org/10.1002/chin.199111122
https://doi.org/10.1002/chin.199111122
Publikováno v:
Synthetic Communications. 20:2083-2090
Various α,α,α-trichloromethylcarbonyl compounds, namely chloral, trichloroacetone, trichloroacetophenone and benzyltrichloromethyl acetate are used in alkaline medium as acylating reagents for primary and secondary amides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54dc433660d058fb229fbcf57bda10da
https://doi.org/10.1080/00397919008053142
https://doi.org/10.1080/00397919008053142
Publikováno v:
ChemInform. 21
The reactivity of N-aryltrichloroacetamides as in situ generating isocyanates is used in the reaction with aminocarboxylic acids and their esters. N-aryl ureido-carboxylic acids, their esters or hydantoins are the obtained compounds.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aee5ba3d4c9db5314265faef58fbb84d
https://doi.org/10.1002/chin.199017141
https://doi.org/10.1002/chin.199017141
Publikováno v:
Synthetic Communications. 19:147-153
Treatment of N-benzylated trichloroacetamides 4, obtained by three different procedures, with potassium carbonate in dimethylsulfoxide affords simmetrical bisbenzylated ureas 5.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3feafad3d013d41c4b4e19c1224dac49
https://doi.org/10.1080/00397918908050963
https://doi.org/10.1080/00397918908050963
Publikováno v:
Synthetic Communications. 19:2947-2954
The reactivity of N-aryltrichloroacetamides as in situ generating isocyanates is used in the reaction with aminocarboxylic acids and their esters. N-aryl ureido-carboxylic acids, their esters or hydantoins are the obtained compounds.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14237554fb413a1f849fdafbb292b331
https://doi.org/10.1080/00397918908052688
https://doi.org/10.1080/00397918908052688
Publikováno v:
Monatshefte f�r Chemie. 94:904-913
Bei der Umsetzung von Hydrobenzamid mit dem Methyl-oder Athylester der Phenylessigsaure in Gegenwart von wasserfr. AlCl3 entstanden hauptsachlich die Ester der diastereomerendl-3-Amino-2,3-diphenylpropansauren neben geringen Mengen der einen freiendl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5acad18ea0cea145c729aa4f56f0e56f
https://doi.org/10.1007/bf00902363
https://doi.org/10.1007/bf00902363
Publikováno v:
Canadian Journal of Chemistry. 49:139-142
Fumarophycine, an alkaloid derived from Fumaria officinalis of Bulgarian origin, is shown by spectroscopic methods to be a new member of the spiroisoquinoline group. It has been related by chemical methods to the alkaloid, fumaritine, of known consti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e17fbfe8cf32e83125001c6f367b1d08
https://doi.org/10.1139/v71-022
https://doi.org/10.1139/v71-022
Publikováno v:
Monatshefte f�r Chemie. 95:64-73
Die diastereomerendl-3-Amino-2,3-diphenyl-propansauren bzw. ihre Ester werden mittels LiAlH4 in die entsprechendendl-1-Amino-1,2-diphenyl-3-propanole ubergefuhrt. Diethreo-Konfiguration ordnet man dem Diastereomeren zu, das in Losung vorwiegend in du
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18f3a9088c864148d88b5d5275c20727
https://doi.org/10.1007/bf00909253
https://doi.org/10.1007/bf00909253
Publikováno v:
Synthesis. 1987:734-736
Etude de la reaction entre des (N-aryl trichloro) acetamide et les benzamide et benzenesulfonamide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52667cd9d2f76c60d7fb333c5b237b64
https://doi.org/10.1055/s-1987-28067
https://doi.org/10.1055/s-1987-28067
Publikováno v:
Chemischer Informationsdienst. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8edcab47172d5994c7e7e85e636fc50
https://doi.org/10.1002/chin.198644268
https://doi.org/10.1002/chin.198644268