Zobrazeno 1 - 10
of 12
pro vyhledávání: '"John H. Buzby"'
Publikováno v:
Synthetic Communications. 24:427-432
N-Benzylidenebenzenesulfonamide was shown to be a useful benzaldehyde equivalent in the Knoevenagel Reaction for cyana - containing active methylene compunds. The intermediate β-N-benzenesulfonylamino carbonyl derivatives from other active methylene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cf5e385606d8734c0f0d53c6d82f006
https://doi.org/10.1080/00397919408011202
https://doi.org/10.1080/00397919408011202
Publikováno v:
The Journal of Organic Chemistry. 58:6712-6715
The diimine, N,N'-dibenzylidene-2,3-diamino-2,3-dimethylbutane (10), was successfully synthesized from 2,3-diamino-2,3-dimethylbutane (3) by reaction with excess benzaldehyde. The reaction of diimine (10) with permanganate/PTC at pH=4.1 did not give
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96a53309e86908e298038fdfc9bd7a02
https://doi.org/10.1021/jo00076a034
https://doi.org/10.1021/jo00076a034
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5240d50e8628065ad3703d03eb88e272
https://doi.org/10.1002/chin.199412128
https://doi.org/10.1002/chin.199412128
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5deb073361ba8da5186dfb7583f97fd5
https://doi.org/10.1002/chin.199637067
https://doi.org/10.1002/chin.199637067
Publikováno v:
The Journal of Organic Chemistry. 55:3555-3562
A series of carbohydrate-derived dienes with different patterns of substitution on the pyranose ring were synthesized and their Diels-Alder reactions investigated. The diene moiety was incorporated into the pyranose ring by oxidation of 4-O-methanesu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f307e3100b812692ee0e6fda220e53a4
https://doi.org/10.1021/jo00298a033
https://doi.org/10.1021/jo00298a033
Publikováno v:
The Journal of Organic Chemistry. 61:3545-3547
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7858422366a837434b3d81396c6581a8
https://doi.org/10.1021/jo950596m
https://doi.org/10.1021/jo950596m
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e0c5ae0f422d9e0e8360584e83895ea
https://doi.org/10.1002/chin.199030091
https://doi.org/10.1002/chin.199030091
Autor:
John H. Buzby, Robert M. Giuliano
Publikováno v:
Carbohydrate Research. 158:C1-C4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da68ed06321ffa2ad0961755b6a69cfe
https://doi.org/10.1016/0008-6215(86)84026-5
https://doi.org/10.1016/0008-6215(86)84026-5
Autor:
John H. Buzby, Robert M. Giuliano
Publikováno v:
Journal of Carbohydrate Chemistry. 6:541-552
Selective reductions of the aldehyde and alkene functionalities in methyl 2, 3-di-O-benzyl-4-deoxy-β-L-threo-hex-4-enodialdopyranoside (4) are described. The title compound was synthesized in six steps from methyl α-D-glucopyranoside. Catalytic red
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77381c934b18f5621d763a8748f7f38a
https://doi.org/10.1080/07328308708058884
https://doi.org/10.1080/07328308708058884