[O-(5-乙酰氨基-3,5-二脱氧-D-甘油-α-D-半乳糖-2-壬酮糖醛酸)-(2→3)-O-β-D-吡喃半乳糖基-(1→3)-2-乙酰氨基-2-脱氧-D-吡喃半乳糖的合成] - Suppr

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超能文献

[Synthesis of O-(5-acetamido-3,5-dideoxy-D-glycero-alpha-D-galacto-2- nonulo-pyranosyluronic)-(2----3)-O-beta-D-galactopyrano sylp61 ----3)-2-acetamido-2-deoxy-D-galactopyranose].

作者信息

Paulsen H, von Deessen U

机构信息

Institut für Organische Chemie der Universität Hamburg, Bundesrepublik Deutschland.

出版信息

Carbohydr Res. 1988 Apr 15;175(2):283-93. doi: 10.1016/0008-6215(88)84150-8.

DOI:10.1016/0008-6215(88)84150-8

PMID:3401880

Abstract

摘要

相似文献

[Synthesis of O-(5-acetamido-3,5-dideoxy-D-glycero-alpha-D-galacto-2- nonulo-pyranosyluronic)-(2----3)-O-beta-D-galactopyrano sylp61 ----3)-2-acetamido-2-deoxy-D-galactopyranose].[O-(5-乙酰氨基-3,5-二脱氧-D-甘油-α-D-半乳糖-2-壬酮糖醛酸)-(2→3)-O-β-D-吡喃半乳糖基-(1→3)-2-乙酰氨基-2-脱氧-D-吡喃半乳糖的合成]

Carbohydr Res. 1988 Apr 15;175(2):283-93. doi: 10.1016/0008-6215(88)84150-8.

Synthetic mucin fragments: benzyl 2-acetamido-3-O-[3-O-(2-acetamido-2-deoxy-beta-D-glucopyranosyl) -beta-D-galactopyranosyl]-2-deoxy-alpha-D-galactopyranoside.合成粘蛋白片段：苄基 2-乙酰氨基-3-O-[3-O-(2-乙酰氨基-2-脱氧-β-D-吡喃葡萄糖基)-β-D-吡喃半乳糖基]-2-脱氧-α-D-吡喃半乳糖苷。

Carbohydr Res. 1984 Sep 1;132(1):137-41. doi: 10.1016/0008-6215(84)85071-5.

Total synthesis of sialosylcerebroside, GM4.唾液酸神经酰胺（GM4）的全合成

Carbohydr Res. 1987 Jun 15;163(2):209-25. doi: 10.1016/0008-6215(87)80182-9.

Synthesis of a fully protected derivative of O-(N-acetyl-alpha-D-neuraminyl)-(2----3)-O-beta-D-galactopyranosyl-(1- ---3)-O- [(N-acetyl-alpha-D-neuraminyl)-(2----6)]-O-(2-acetamido-2-deoxy-alpha- D-galactopyranosyl)-(1----3)-L-serine.O-（N-乙酰基-α-D-神经氨酰基）-（2→3）-O-β-D-吡喃半乳糖基-（1→3）-O- [（N-乙酰基-α-D-神经氨酰基）-（2→6）]-O-（2-乙酰氨基-2-脱氧-α-D-吡喃半乳糖基）-（1→3）-L-丝氨酸的全保护衍生物的合成

Carbohydr Res. 1989 Feb 15;186(1):107-18. doi: 10.1016/0008-6215(89)84009-1.

Synthesis of a mucin-type O-glycosylated amino acid, beta-Gal-(1----3)-[alpha-Neu5Ac-(2----6)]-alpha-GalNAc-(1----3)- Ser.一种粘蛋白型O-糖基化氨基酸β-Gal-(1→3)-[α-Neu5Ac-(2→6)]-α-GalNAc-(1→3)-丝氨酸的合成

Carbohydr Res. 1989 Feb 15;186(1):95-106. doi: 10.1016/0008-6215(89)84008-x.

Chemoenzymatic synthesis of the sialyl-alpha-(2-->3')-lactosamine trisaccharide with a 3-aminopropyl group as a spacer at the reducing end.以3-氨丙基作为还原端间隔基团的唾液酸-α-(2→3')-乳糖胺三糖的化学酶法合成。

Carbohydr Res. 2003 Jun 16;338(12):1265-70. doi: 10.1016/s0008-6215(03)00167-8.

Synthesis and NMR spectroscopic investigation of oligosaccharides containing Kdo and L-glycero-D-manno-heptopyranosyl residues.含有Kdo和L-甘油-D-甘露庚糖残基的寡糖的合成及核磁共振光谱研究

Carbohydr Res. 1993 May 7;243(2):273-91. doi: 10.1016/0008-6215(93)87033-o.

Synthetic mucin fragments: methyl 3-O-(2-acetamido-2-deoxy-beta-D-galactopyranosyl-beta-D- 3-O-(2-acetamido-2-deoxy-3-O-beta-D-galactopyranosyl- beta-D-glucopyranosyl)-beta-D-galactoyranoside. pyranosyl)-beta-D-galactopyranoside.合成粘蛋白片段：3-O-（2-乙酰氨基-2-脱氧-β-D-吡喃半乳糖基）-β-D-吡喃半乳糖苷甲酯。3-O-（2-乙酰氨基-2-脱氧-3-O-β-D-吡喃半乳糖基-β-D-吡喃葡萄糖基）-β-D-吡喃半乳糖苷。

Carbohydr Res. 1984 Sep 1;132(1):127-35. doi: 10.1016/0008-6215(84)85070-3.

Chemical synthesis of the desialylated human Cad-anti-genic determinant.去唾液酸人Cad抗原决定簇的化学合成

Carbohydr Res. 1986 Nov 1;155:131-40. doi: 10.1016/s0008-6215(00)90139-3.

Synthesis of 4-nitrophenyl O-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)- (1-->2)-O-(6-O-methyl-alpha-D-mannopyranosyl)-(1-->6)-beta-D- glucopyranoside and its 4',6'-di-O-methyl analog. Potential inhibitors of N-acetylglucosaminyl-transferase V (GnT-V).4-硝基苯基 O-(2-乙酰氨基-2-脱氧-β-D-吡喃葡萄糖基)-(1→2)-O-(6-O-甲基-α-D-吡喃甘露糖基)-(1→6)-β-D-吡喃葡萄糖苷及其 4',6'-二-O-甲基类似物的合成。N-乙酰葡糖胺基转移酶 V（GnT-V）的潜在抑制剂。

Carbohydr Res. 1993 Apr 23;243(1):29-42. doi: 10.1016/0008-6215(93)84079-l.

引用本文的文献

Sequential two-step multienzyme synthesis of tumor-associated sialyl T-antigens and derivatives.肿瘤相关唾液酸化 T 抗原及其衍生物的两步顺序多酶合成。

Org Biomol Chem. 2011 Apr 21;9(8):2784-9. doi: 10.1039/c0ob01269f. Epub 2011 Mar 1.

Synthesis of phosphites and phosphates of neuraminic acid and their glycosyl donor properties--convenient synthesis of GM3.神经氨酸的亚磷酸酯和磷酸酯的合成及其糖基供体性质——GM3的简便合成

Glycoconj J. 1993 Feb;10(1):16-25. doi: 10.1007/BF00731182.

Processing O-glycan core 1, Gal beta 1-3GalNAc alpha-R. Specificities of core 2, UDP-GlcNAc: Gal beta 1-3 GalNAc-R(GlcNAc to GalNAc) beta 6-N-acetylglucosaminyltransferase and CMP-sialic acid: Gal beta 1-3GalNAc-R alpha 3-sialyltransferase.O-聚糖核心1（Galβ1-3GalNAcα-R）的加工。核心2的特异性，UDP-N-乙酰葡糖胺：Galβ1-3GalNAc-R（从GlcNAc到GalNAc）β6-N-乙酰葡糖胺基转移酶和CMP-唾液酸：Galβ1-3GalNAc-Rα3-唾液酸转移酶。

Glycoconj J. 1993 Oct;10(5):381-94. doi: 10.1007/BF00731043.

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