Zobrazeno 1 - 10
of 103
pro vyhledávání: '"Yuzo Inouye"'
Publikováno v:
Angewandte Chemie. 94:465-466
Das vollstandige Manuskript dieser Zuschrift erscheint in: Angew. Chem. Suppl. 1982, 1021. DOI: 10.1002/ange.198210210
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e32867366cc3ecf9954d46236420cdb8
https://doi.org/10.1002/ange.19820940631
https://doi.org/10.1002/ange.19820940631
Publikováno v:
Tetrahedron Letters. 20:1683-1686
Asymmetric reduction of α-ketoester with a chiral dihydronicotinamide was significantly affected by chiral aromatic additives, capable of exerting an attractive interaction with dihydropyridine ring, which was further consolidated through with magne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f34ea39f885a9b618fcb0b53bc1952c
https://doi.org/10.1016/s0040-4039(01)93623-8
https://doi.org/10.1016/s0040-4039(01)93623-8
Publikováno v:
Agricultural and Biological Chemistry. 39:2065-2068
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0487943c91712c1c456a225dc072a98
https://doi.org/10.1080/00021369.1975.10861887
https://doi.org/10.1080/00021369.1975.10861887
Publikováno v:
Agricultural and Biological Chemistry. 39:2065-2068
The enantioselective addition of chiral benzylic amines to dimethyl maleate and fumarate gives optically active aspartic acid in satisfactory yields. The re-face favorably meets the stereochemical requirements of the chiral R-amines than does the si-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::936d0aca57266d6da5ffaf2013eb14e3
https://doi.org/10.1271/bbb1961.39.2065
https://doi.org/10.1271/bbb1961.39.2065
Publikováno v:
Agricultural and Biological Chemistry. 41:201-204
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b60339473c7acd42de7807a73d5af41
https://doi.org/10.1080/00021369.1977.10862448
https://doi.org/10.1080/00021369.1977.10862448
Publikováno v:
The Journal of Organic Chemistry. 41:300-303
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e0da80c712c272ee9fa883ae1496923
https://doi.org/10.1021/jo00864a024
https://doi.org/10.1021/jo00864a024
Asymmetric reduction of α,β-unsaturated iminium salts with 1,4-dihydronicotinamide sugar pyranosides
Publikováno v:
Canadian Journal of Chemistry. 58:387-392
3,3,5-Trimethyl-2-cyclohexylidene iminium salts were reduced with 1,4-dihydronicotinamide sugar pyranosides to give optically active 3,3,5-trimethylcyclohexanone in enantiomeric excess ranging over 3–31%. The product stereochemistry changed sensiti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07162f25312d12e873cd6a7e8aaa21dd
https://doi.org/10.1139/v80-062
https://doi.org/10.1139/v80-062
Publikováno v:
The Journal of Organic Chemistry. 48:1370-1373
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a07ec810fb585b50409e92819309ead0
https://doi.org/10.1021/jo00156a051
https://doi.org/10.1021/jo00156a051
Publikováno v:
Tetrahedron Letters. 19:3107-3110
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15e7950b9ca6f97c0635c0d6ea22bb87
https://doi.org/10.1016/s0040-4039(01)94955-x
https://doi.org/10.1016/s0040-4039(01)94955-x
Publikováno v:
Israel Journal of Chemistry. 25:236-240
Asymmetric reduction of ethyl benzoylformate were conducted using chiral NADH model compounds with various substituents at the 3- and N1-positions of the dihydronicotinamide. In one case, in which l-prolinamide resides at the terminal of the N1-subst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27f1b2f801a33f3db7054103f1e3a6cf
https://doi.org/10.1002/ijch.198500037
https://doi.org/10.1002/ijch.198500037