標題: Titlebook: Carbohydrate Chemistry; D. R. Bundle,G. Descotes,J. Thiem Conference proceedings 1990 Springer-Verlag Berlin Heidelberg 1990 Chemical synt [打印本頁] 作者: sulfonylureas 時間: 2025-3-21 18:08
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)學科排名
書目名稱Carbohydrate Chemistry網(wǎng)絡公開度
書目名稱Carbohydrate Chemistry網(wǎng)絡公開度學科排名
書目名稱Carbohydrate Chemistry被引頻次
書目名稱Carbohydrate Chemistry被引頻次學科排名
書目名稱Carbohydrate Chemistry年度引用
書目名稱Carbohydrate Chemistry年度引用學科排名
書目名稱Carbohydrate Chemistry讀者反饋
書目名稱Carbohydrate Chemistry讀者反饋學科排名
作者: 笨重 時間: 2025-3-21 21:27 作者: 蹣跚 時間: 2025-3-22 02:48
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.作者: libertine 時間: 2025-3-22 08:37 作者: SKIFF 時間: 2025-3-22 11:32
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.作者: FIS 時間: 2025-3-22 15:14 作者: FIS 時間: 2025-3-22 18:33
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.作者: Ambulatory 時間: 2025-3-22 21:20
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.作者: Monocle 時間: 2025-3-23 05:22 作者: 暫時中止 時間: 2025-3-23 08:43
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作者: 縮影 時間: 2025-3-23 10:15
Synthesis of glycolipids,s of the complete glycosphingolipids) and of myoinositol-containing lipids derived from esters of glycerol, which were reported between 1977 and 1987, are reviewed. This article therefore brings up to date a previous review published in Chemistry and Physics of Lipids (1980) 26: 287. Since this is a作者: engrossed 時間: 2025-3-23 14:58 作者: Antimicrobial 時間: 2025-3-23 18:43 作者: 改正 時間: 2025-3-23 23:31 作者: 灰心喪氣 時間: 2025-3-24 04:05
Syntheses of deoxy oligosaccharides,owing a short review on the biosynthesis of these sugars, the general techniques including classical methods as well as recent stereospecific procedures for the preparation of deoxy glycosides are outlined..For these oligosaccharide-containing pharmaceuticals, brief explanations of their current emp作者: 地牢 時間: 2025-3-24 09:55 作者: anthesis 時間: 2025-3-24 12:25 作者: 哺乳動物 時間: 2025-3-24 16:26 作者: 夜晚 時間: 2025-3-24 21:51 作者: 惡心 時間: 2025-3-25 02:20
https://doi.org/10.1007/BFb0111557Chemical synthesis; Chemische Synthese; Oligosaccarid; Oligosaccharid; carbohydrate chemistry; chemistry; 作者: 品嘗你的人 時間: 2025-3-25 06:49
978-3-662-15053-5Springer-Verlag Berlin Heidelberg 1990作者: 行乞 時間: 2025-3-25 10:39
Preparation of selectively alkylated saccharides as synthetic intermediates,ing groups known, only those widely used in synthetic chemistry of saccharides are discussed. Benzyl, allyl, triphenylmethyl and other arylalkyl ethers, trimethylsilyl, .-butyldimethylsilyl, and .-butyldiphenylsilyl ethers are the main topics of the article.作者: occult 時間: 2025-3-25 13:29
https://doi.org/10.1007/1-84628-186-5es, comparatively rare monosaccharides. The oligosaccharides that constitute the repeating units of these polysaccharide antigens provide a demanding challenge in terms of glycoside synthesis, an objective which is particularly important since these structures act as antigenic determinants which are作者: Progesterone 時間: 2025-3-25 18:40 作者: Cabinet 時間: 2025-3-25 23:52 作者: Crohns-disease 時間: 2025-3-26 03:43
Multi-Dimensional Slow-Fast Systems,Conformational analysis of oligosaccharides makes the three dimensional structure available. The analysis of the conformation of oligosaccharides is usually determined by a combination of computational methods and experimental techniques. NMR spectroscopy is the most important experimental tool. The作者: 匍匐 時間: 2025-3-26 07:31 作者: Needlework 時間: 2025-3-26 09:13 作者: 絕緣 時間: 2025-3-26 13:07 作者: needle 時間: 2025-3-26 17:56 作者: keloid 時間: 2025-3-26 21:08
Multi-Dimensional Slow-Fast Systems,. This review covers conformational analyses of blood group antigens of .-linked and of .-linked oligosaccharide chains, of glycolipids, of oligosaccharides related to O-specific polysaccharides of bacteria, and of oligosaccharides related to proteoglycans.作者: debble 時間: 2025-3-27 03:00
Synthesis of oligosaccharides related to bacterial O-antigens,ating units. The most intensive synthetic efforts have focused on the O-antigens of ., and ., although increasing attention is being given to the synthesis of antigenic determinants of other Gram-negative pathogens, including those of ..作者: Abominate 時間: 2025-3-27 07:20
Conformational aspects of oligosaccharides,. This review covers conformational analyses of blood group antigens of .-linked and of .-linked oligosaccharide chains, of glycolipids, of oligosaccharides related to O-specific polysaccharides of bacteria, and of oligosaccharides related to proteoglycans.作者: 頂點 時間: 2025-3-27 13:02
9樓作者: 寬度 時間: 2025-3-27 17:01
9樓作者: 他很靈活 時間: 2025-3-27 18:55
9樓作者: 誓言 時間: 2025-3-27 23:39
10樓作者: CANON 時間: 2025-3-28 03:49
10樓作者: 獸皮 時間: 2025-3-28 08:55
10樓作者: Deject 時間: 2025-3-28 11:41
10樓
