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1)  chiral alcohol
手性醇
1.
Asymmetric reduction carbonyl compounds to chiral alcohols by baker's yeast;
面包酵母催化羰基不对称还原合成手性醇的研究
2.
Progress of asymmetric reduction of chiral alcohol with genetic engineering strain;
基因工程菌在不对称还原制备手性醇中的应用进展
3.
Asymmetric reduction of prochiral ketone to these chiral alcohols by active microbe cells is one of the most promising routes.
以4-氯苯乙酮(C l-ACP)为苯环上含卤素的芳香酮的模型底物,研究了活性酵母细胞在水相体系中催化该类芳香酮不对称还原合成相应手性醇的反应特性。
2)  chiral amino alcohol
手性胺醇
1.
Three new C2-symmetric chiral amino alcohols (PhOHCHCH2)2NCH2C6H4R (R=OCH3, L1; R=CH3, L2; R=Cl, L3) and their lanthanide complexes LLnCl·2THF (L=L1, L2, L3; Ln=La, Sm, Gd) were prepared and characterized.
合成了三种新的含C2-对称轴的手性胺醇(PhOHCHCH2)2NCH2C6H4R(R=OCH3,L1;R=CH3,L2;R=Cl,L3),将其与无水氯化稀土LnCl3·4THF(Ln=La,Sm,Gd)反应生成了九个新的胺醇类稀土配合物LLnCl·2THF(L=L1,L2,L3;Ln=La,Sm,Gd)。
3)  chiral diol
手性二醇
1.
Some chiral diols were also investigated as the ligands, with those derived from indene exhibiting better enantioselectivity.
又考察一些手性二醇配体,其中,茚衍生的配体有着较好的手性诱导性能。
4)  chiral cyanohydrins
手性氰醇
5)  D-Chiro-Inositol
手性肌醇
1.
TLC determination method research of D-Chiro-Inositol in buckwheat seed;
荞麦籽粒中手性肌醇的薄层层析定性检测方法研究
2.
Determination of D-Chiro-Inositol in Fagopyrum tataricum Seed by RP-HPLC
反相高效液相色谱法测定选荞1号中的手性肌醇
3.
Using gas chromatography-mass spectrometry (GC-MS), gas chromatography (GC) an d high performance liquid chromatography (HPLC), the soluble carbohydrates were identified as D-chiro-inositol (DCI), fructose, glucose, sorbitol, myo-inositol, sucrose, ethyl-β-rutinoside and two unknown substances in the extracts of different milling fractions of Fagopyrum tataricum seeds.
通过气相色谱 质谱联用、气相色谱、高效液相色谱等手段,在苦荞籽粒中检测出了手性肌醇(DCI)、木糖醇、果糖、葡萄糖、山梨醇、肌醇、蔗糖、乙基 β 芸香糖苷等可溶性糖(醇)和两种未知化合物,苦荞籽粒各部分(壳、麸皮、外层粉、心粉)所含糖(醇)种类基本相同。
6)  chiral secondary alcohol
手性仲醇
补充资料:手性碳原子
分子式:
CAS号:

性质:又称不对称碳原子(asymmetric carbon atom),即连有4个不同原子或基团的碳原子。如HC*FClBr(常以*标记手性碳原子)。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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