Titlebook: Carbohydrate Chemistry; D. R. Bundle,G. Descotes,J. Thiem Conference proceedings 1990 Springer-Verlag Berlin Heidelberg 1990 Chemical synt

sulfonylureas

書目名稱Carbohydrate Chemistry影響因子(影響力)




書目名稱Carbohydrate Chemistry影響因子(影響力)學(xué)科排名




書目名稱Carbohydrate Chemistry網(wǎng)絡(luò)公開度




書目名稱Carbohydrate Chemistry網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Carbohydrate Chemistry被引頻次




書目名稱Carbohydrate Chemistry被引頻次學(xué)科排名




書目名稱Carbohydrate Chemistry年度引用




書目名稱Carbohydrate Chemistry年度引用學(xué)科排名




書目名稱Carbohydrate Chemistry讀者反饋




書目名稱Carbohydrate Chemistry讀者反饋學(xué)科排名

笨重

蹣跚

Deterministic Slow-Fast Systems, stereoelectronic factors. The preferential α-attack of anomeric radicals is a well documented example of such transformations..Some new methodologies using single electron transfer reactions are also indicated in this review.

libertine

SKIFF

https://doi.org/10.1007/1-84628-186-5crylic acid. The Diels-Alder adduct was readily resolved by means of optically active amines as resolution reagents into the two antipodes, which were then used as starting compounds for the synthesis of enantiomeric pseudo-sugars. Also, a chiral synthesis from true sugars has been used for the preparation of enantiomeric pseudo-sugars.

FIS

FIS

Synthesis of glycolipids, very active field of research, most of the new synthetic techniques introduced into carbohydrate chemistry in the last decade are discussed. The syntheses of sphingosine bases and glycerol derivatives from carbohydrate precursors acting as ‘chiral templates’ are also reviewed with a more historical perspective.

Ambulatory

Chemistry of pseudo-sugars,crylic acid. The Diels-Alder adduct was readily resolved by means of optically active amines as resolution reagents into the two antipodes, which were then used as starting compounds for the synthesis of enantiomeric pseudo-sugars. Also, a chiral synthesis from true sugars has been used for the preparation of enantiomeric pseudo-sugars.

Monocle

暫時(shí)中止

Synthetic saccharide photochemistry,xidation reactions. The use of photoremovable protecting groups in osidic syntheses is also evoked..The recent development of such radical reactions using photoinitiators is mainly due to their regio and stereoselectivities interpreted in terms of stabilized conformations of carbohydrate radicals by