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Absolute configuration of the carboxyethyl (lactyl) side chain of muramic acid [2-amino-3-O-(D-1 carboxyethyl)-2-deoxy-D-glucose].

作者信息

Veyrières A, Jeanloz R W

出版信息

Biochemistry. 1970 Oct 13;9(21):4153-9. doi: 10.1021/bi00823a018.

DOI:10.1021/bi00823a018
PMID:4318804
Abstract
摘要

相似文献

1
Absolute configuration of the carboxyethyl (lactyl) side chain of muramic acid [2-amino-3-O-(D-1 carboxyethyl)-2-deoxy-D-glucose].胞壁酸[2-氨基-3-O-(D-1-羧乙基)-2-脱氧-D-葡萄糖]羧乙基(乳酸基)侧链的绝对构型
Biochemistry. 1970 Oct 13;9(21):4153-9. doi: 10.1021/bi00823a018.
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Structural studies of 4-acetamido-2-amino-2,4,6-trideoxy-D-glucose (N-acetylbacillosamine), the N-acetyldiamino sugar of Bacillus licheniformis.地衣芽孢杆菌的N-乙酰二氨基糖4-乙酰氨基-2-氨基-2,4,6-三脱氧-D-葡萄糖(N-乙酰芽孢胺)的结构研究
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Arch Biochem Biophys. 1968 Feb;123(2):240-6. doi: 10.1016/0003-9861(68)90130-6.
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Synthesis of muramic acid 6-phosphate (2-amino-3-O-(D-1-carboxyethyl)-2-deoxy-D-glucose 6-(dihydrogen phosphate)).磷酸穆糖酸(2-氨基-3-O-(D-1-羧乙基)-2-脱氧-D-葡萄糖6-(磷酸二氢酯))的合成
Biochemistry. 1971 Jan 5;10(1):192-6. doi: 10.1021/bi00777a028.
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AN IMPROVED, STEREOSELECTIVE SYNTHESIS OF 2-AMINO-3-O-(D-1-CARBOXYETHYL)-2-DEOXY-D-GLUCOSE (MURAMIC ACID).2-氨基-3-O-(D-1-羧乙基)-2-脱氧-D-葡萄糖(胞壁酸)的一种改进的立体选择性合成方法
J Org Chem. 1965 Feb;30:448-50. doi: 10.1021/jo01013a037.
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Characterization of the 4-acetamido-4,6-dideoxyhexoses from Escherichia coli strains.大肠杆菌菌株中4-乙酰氨基-4,6-二脱氧己糖的特性分析。
J Biol Chem. 1973 Jan 10;248(1):104-9.
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The synthesis of guanosine 5'-diphosphate D-rhamnose.
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Synthesis of the four pairs of side-chain epoxides epimeric at carbon 20 derived from 5-beta-pregnan-3-alpha-ol.
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Structures and activities of oligosaccharides produced by alkaline degradation of a blood group substance lacking A, B, H, Le b specificities.
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The oxidation of 2-acetamido-2-deoxyaldoses with aqueous bromine. Two diastereoisomeric 2-acetamido-2,3-dideoxyhex-2-enono-1,4-lactones from 2-acetamido-2-deoxy-D-glucose, -mannose, and -galactose.用溴水氧化2-乙酰氨基-2-脱氧醛糖。由2-乙酰氨基-2-脱氧-D-葡萄糖、-甘露糖和-半乳糖生成两种非对映异构的2-乙酰氨基-2,3-二脱氧己-2-烯糖酸-1,4-内酯。
Carbohydr Res. 1971 Oct;19(3):339-52. doi: 10.1016/s0008-6215(00)86164-9.