[有化]氨基醇
alcohol───n.酒精,乙醇
amino acids───[生化]氨基酸(aminoacid的复数);n.氨基酸( amino acid的名词复数 ); 氨基酸类
amino acid───n.[生化]氨基酸;n.氨基酸
gnaws alcohol───啃酒
alcohol abuse───酒精滥用,酗酒
spirituous alcohol───烈酒
alcohol poisoning───醇类中毒
headers amino───头部氨基
drugging alcohol───麻醉酒精
A basic, long-chain, unsaturated amino alcohol, C18H 37NO 2, found combined with lipids in the brain and in nerve tissue.───一种不饱合的长链氨基醇,化学式为C18H 37NO 2,与脂结合而存在于脑中或神经组织中。
Chiral amino alcohol is a kind of the ligand or catalyst with great potential for the development of catalytic asymmetric synthesis.───手性氨基醇是一类具有很大发展潜力的用于催化不对称合成反应的配体或催化剂。
Synthesis of new chiral amino alcohol derived from camphor;───制备合成龙脑与合成樟脑的新工艺。
The results indicate that the larger steric hindrance in the amino alcohol unit of Schiff base ligands leads to higher enantioselectivity.───结果表明,氨基醇部分的结构空间位阻越大,产物亚砜的对映选择性越高;
Two types of C2 symmetric chiral ligands, namely, chiral Schiff bases and chiral amino alcohol, have been prepared.───本项目制备了两类具有C2对称的手性配体,即手性席夫碱和手性胺醇。
Synthesis of a Polymer(fiber)-Supported Chiral Amino Alcohol and Its Application to Enantioselective Addition of Diethylzinc to Benzaldehyde───高分子(纤维)负载手性氨基醇的合成及其催化二乙基锌对苯甲醛的不对称加成
Synthesis and Fluorescence of Chiral Amino Alcohol Lanthanide Complexes and Their Catalytic Asymmetric Hydrogenation for Aromatic Ketones───手性胺醇稀土配合物的合成、荧光性质及其催化芳香酮的不对称氢化反应
Accurate Mass Determination of Amino Alcohol Derivatives by Turboionspray-Time-of-flight Mass Spectrometry───电喷雾-飞行时间质谱测定氨基醇类化合物及衍生物的准确质量
Synthesis and Characterization of Chiral Oxygen Nucleophile of Amino-alcohol───氨基醇类手性氧亲核试剂的合成及表征
Chiral amino alcohol has extensively applicates in the asymmetric synthesis and intermediate areas, and a lot of scientific research personnel have deep interests in it .
Chiral amino alcohol is a kind of the ligand or catalyst with great potential for the development of catalytic asymmetric synthesis.
A basic, long-chain, unsaturated amino alcohol, C18H 37NO 2, found combined with lipids in the brain and in nerve tissue.
Two N-monoalkyl and N-dialkyl novel chiral amino alcohol ligands with different configuration were prepared.
The results indicate that the larger steric hindrance in the amino alcohol unit of Schiff base ligands leads to higher enantioselectivity.
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