Zobrazeno 1 - 10
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pro vyhledávání: '"Nagabushanam Kalyanam"'
Publikováno v:
Tetrahedron Letters. 54:5155-5158
Ornithine methyl ester reacts with aromatic aldehydes to generate bis-Schiff bases, which depending on the structure of the aromatic aldehyde, further undergo an intramolecular cycloaddition through the transient formation of a reactive 1,3-dipole.
Publikováno v:
Tetrahedron: Asymmetry. 24:663-668
The synthesis of chemically and enantiomerically pure (S)-3-amino tetrahydrofuran hydrochloride starting from the natural amino acids, l -aspartic acid or l -methionine is described. The process involves no chromatography and can be easily carried ou
Publikováno v:
ChemInform. 45
Ornithine methyl ester reacts with aromatic aldehydes to generate bis-Schiff bases, which depending on the structure of the aromatic aldehyde, further undergo an intramolecular cycloaddition through the transient formation of a reactive 1,3-dipole.
Publikováno v:
ChemInform. 22
A reaction of tetrahydro-1,5-benzodiazepines with aromatic aldehydes which yields the hitherto unknown 1,5-methanotetrahydro-1,5-benzodiazepines as a single stereoismer is described. The stereochemistry of the products is established using proton nmr
Autor:
Nagabushanam Kalyanam, Muhammed Majeed
Publikováno v:
ChemInform. 40
A readily available γ-glutamyl transfer reagent, namely, N-phthaloyl-L-glutamic anhydride (NPGLA.) offers a simple solution for the raceinization free synthesis of γ-glutamyl amino acids with usefully enhanced properties γ-glutamyi dipeptides (γ-
Publikováno v:
ChemInform. 40
Akademický článek
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Publikováno v:
HETEROCYCLES. 51:237
Publikováno v:
HETEROCYCLES. 51:2119
Publikováno v:
HETEROCYCLES. 32:1131
A reaction of tetrahydro-1,5-benzodiazepines with aromatic aldehydes which yields the hitherto unknown 1,5-methanotetrahydro-1,5-benzodiazepines as a single stereoismer is described. The stereochemistry of the products is established using proton nmr