Synthesis of sialic acid derivatives based on chiral substrate-controlled stereoselective aldol reactions using pyruvic acid oxabicyclo[2.2.2]octyl orthoester
accomplished based on substrate-controlled asymmetric aldol reactions between sterically complicated aldehydes easily prepared from commercially available carbohydrates and a novel pyruvic acid oxabicyclo[2.2.2]octyl orthoester. Systematic aldol reactionstudies using chiral aldehydes revealed that α,β,γ-benzyloxy-substituted aldehydes with an α,β-anti relative configuration preferentially provided the
唾液酸及其类似物的合成是基于易于从市售碳水化合物制备的空间复杂醛与新型丙酮酸草酸双环[2.2.2]辛基原酸酯之间的受底物控制的不对称醛醇缩合反应完成的。使用手性醛的系统羟醛反应研究表明,具有α,β-反相对构型的α,β,γ-苄氧基取代的醛优先为Felkin产物提供具有高非对映选择性的4,5-抗构型。具有α,β-顺式排列的α,β,γ-苄氧基取代的醛中的相对β,γ构型对醛醇缩合反应中形成的立构中心的非对映选择性具有次要作用。syn - β ,γ-抗苄氧基醛显示出比α,β- syn - β ,γ- syn苄氧基醛更高的非对映选择性,从而生成Felkin产物。
A mild and general method for preparation of α-glycosyl chlorides
作者:Chih-Wei Chang、Shih-Sheng Chang、Chin-Sheng Chao、Kwok-Kong T. Mong
DOI:10.1016/j.tetlet.2009.05.077
日期:2009.8
A mild and efficient chlorination method for production of glycosyl chlorides is first described which employs inexpensive trichlorotriazine (TCT) and DMF as a chlorination reagent and is compatible with typical acid-labile hydroxyl protecting functions. The scope and limitations, reaction mechanism and its application in the sequential glycosylations are discussed. (C) 2009 Elsevier Ltd. All rights reserved.
[EN] CONJUGATES OF A GLYCOPROTEIN OR A GLYCAN WITH A TOXIC PAYLOAD<br/>[FR] CONJUGUÉS D'UNE GLYCOPROTÉINE OU D'UN GLYCANE AVEC UNE CHARGE TOXIQUE
申请人:GLYKOS FINLAND OY
公开号:WO2014177771A1
公开(公告)日:2014-11-06
The invention relates to a glycoprotein-toxic pay- load molecule conjugate, a toxic payload molecule- glycan conjugate, and a pharmaceutical composi- tion.The invention further relates to a method for preparing the glycoprotein-toxic payload mole- cule conjugate, the method for modulating growth of a cell population and a method of treating tu- mour cells.