1) chiral aminodiol
手性氨基二醇
1.
A first step is made to synthesize a kind of chiral aminodiol via reduction .
并对手性氨基二醇的合成途径进行了初步的探讨 ,合成了一种新型的手性氨基二醇 。
2) chiral ferrocenyl β-amino alcohols
手性二茂铁基β-氨基醇
3) Chiral amino alcohols
手性氨基醇
1.
The applications and recent progresses of chiral amino alcoholsas either ligands or catalysts in asymmetric synthesis are reviewed.
综述了手性氨基醇作为配体或催化剂在不对称合成中的应用及最新进展。
2.
Chiral amino alcohols are a class of optically active amino alcohols obtained by the reduction of α-amino acids as starting materials.
手性氨基醇是一类由α-氨基酸经过手性源还原得到的具有光学活性的氨基醇。
3.
A series of novel chiral amino alcohols containing benzimidazole group were synthesized by the reaction of D-phenylglycinol with different substituted 2-chlorobenzimidazole which were synthesized by bromination and nitration.
以2-氯苯并咪唑为原料,通过硝化反应和溴化反应,分别合成其硝化和溴化产物;再以二异丙基乙氨为溶剂,和D-苯甘氨醇反应,合成了一系列新型含苯并咪唑手性氨基醇类化合物,并对各产物进行了核磁共振(NMR)、红外(IR)、质谱(MS)表征。
4) chiral aminoalcohol
手性氨基醇
1.
In view of those properties, chiral aminoalcohol's serial products are steadily on the increase and show the great capacity of the potential market in the world.
手性氨基醇在不对称合成领域中是一类重要的手性源,同时,手性氨基醇在药物合成、外消旋体拆分等领域也具有广泛的用途。
5) chiral amino alcohol
手性氨基醇
1.
Synthesis of new chiral amino alcohol derived from camphor;
樟脑衍生的新手性氨基醇的合成
2.
methyl-pyrrolidine-2-ylmethyl)-amino]-1,1,3-triphenyl-propan-1-ol (6) synthesized from natural amino acids is a new multifunctional chiral amino alcohol ligand.
以天然手性氨基酸为原料 ,合成了一个新的多官能团手性氨基醇配体 ,并用红外、核磁、元素分析等测试方法确定了该化合物的结
3.
These chiral amino alcohols were first applied to the asymmetric reduction of acetophenone.
合成了（１Ｒ，２Ｓ）－１－二丁基氨基－１，２－二氢－２－茚醇及其对映体，首次将此类手性氨基醇用于苯乙酮的不对称还原反应研究，用温和的还原剂ＫＢＨ４，得到的还原产物１－苯基乙醇其最佳对映体过量值达８１％。
6) chiral β-aminoalcohol
手性β-氨基醇
1.
Application of a new chiral β-aminoalcohol in catalytic asymmetric addition of carbonyl compounds;
新型手性β-氨基醇在羰基化合物催化不对称加成反应中的应用
2.
Starting from correspongding olefins, eight chiral β-aminoalcohols were synthesized by Shar-pless asymmetric dihydroxylation and applied in the organocatalytic asymmetric epoxidation of α,β-enones.
将以烯烃为原料通过Sharpless不对称双羟化等多步反应合成的8种手性β-氨基醇,作为有机小分子催化剂,用于催化α,β-不饱和酮的不对称环氧化反应。
3.
Seven chiral β-aminoalcohols were synthesized by Sharpless asymmetric dihydroxylation and used as chiral catalysts in the asymmetric addition of diethylzinc to aldehydes.
以烯烃为原料通过Sharpless不对称双羟化等多步反应合成7种手性β-氨基醇,并将该类化合物用于催化二乙基锌和醛的不对称加成反应。
补充资料：己二酸、1,4-丁二醇、异癸醇、新戊二醇生成酯
CAS：84777-46-8
中文名称：己二酸、1,4-丁二醇、异癸醇、新戊二醇生成酯
英文名称：Hexanedioic acid, mixed esters with 1,4-butanediol, isodecanol and neopentyl glycol
中文名称：己二酸、1,4-丁二醇、异癸醇、新戊二醇生成酯
英文名称：Hexanedioic acid, mixed esters with 1,4-butanediol, isodecanol and neopentyl glycol
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条