Zobrazeno 1 - 10
of 33
pro vyhledávání: '"M. A. M. NASSR"'
Publikováno v:
ChemInform. 23
Publikováno v:
ChemInform. 23
Publikováno v:
Journal of Carbohydrate Chemistry. 11:305-318
Reaction of 1-(2,3,4,5-tetra-o-acetylgalactaroy1)bis-2-[thiomethyl or thiobenzy1(thiocarbony1)]hydrazine 1 or 2 with different bifunctional amines [piperazine (PPZ), tetraethyl-ethylenediamine (TEED), tetramethylethylenediamine (TMED), and tetramethy
Publikováno v:
Journal f�r Praktische Chemie. 333:339-344
The syntheses of galactaric acid acetate bis[alkylthio-(thiocarbonyl)]hydrazides (1,2) are described. Selective cyclisation of both hydrazide 1 and 2 was investigated. Using phosphorous oxychloride as a cyclising agent, loss of water produced 1,2,3,4
Publikováno v:
Journal of Carbohydrate Chemistry. 10:429-438
The syntheses of galactaric acid acetate bis[alkylthio-(thiocarbonyl)]hydrazides (1,2) are described. Selective cyclisation of both hydrazide 1 and 2 was investigated. Using phosphorous oxychloride as a cyclising agent, loss of water produced 1,2,3,4
Publikováno v:
Carbohydrate Research. 121:119-124
d -Glucono-1,5-lactone reacts with aroylhydrazines to give the corresponding 1-aroyl-2- d -gluconylhydrazines. Condensative cyclization of these compounds using triethyl orthoformate gave the corresponding 5-aryl-2-ethoxy-3- d -gluconyl-2,3-dihydro-1
Publikováno v:
Journal of the Chinese Chemical Society. 32:65-73
Opianic acid reacts with various hydrazines to yield either hydrazone (3, 6) or phthalazinone (4) derivatives depending upon the electronic properties of the substituent attached to the hydrazine molecule. Oxidative cyclization of opianic acid aroylh
Publikováno v:
Carbohydrate Research. 77:99-105
Condensation of benzyl 2-acetamido-3,6-di- O -benzyl-2-deoxy-α- D -glucopyranoside with 2,3,4,6-tetra- O -benzyl-1- O -( N -methyl)acetimidoyl-β- D -glucopyranose gave benzyl 2-acetamido-3,6-di- O -benzyl-2-deoxy-4- O -(2,3,4,6-tetra- O -benzyl-α-
Publikováno v:
Bulletin of the Chemical Society of Japan. 60:3405-3409
The synthesis of some acyclic C-nucleoside analogs possessing thiadiazole rings was achieved by the heterocyclization of the 4-arylthiosemicarbazones of D-galactose, D-glucose, D-mannose, D-arabinose, and lactose, Acetylation of the thiadiazoles affo
Autor:
M. A. M. Nassr
Publikováno v:
Organic Preparations and Procedures International. 15:329-333