1) Sharpless asymmetric dihydroxylation
Sharpless不对称双羟化反应
2) Sharpless asymmetric dihydroxylation reaction
Sharpless不对称二羟化反应
1.
Two recyclable ligands were prepared and applied to Sharpless asymmetric dihydroxylation reaction in two solvent systems for preparation of ethyl (2R,3S)-2,3-dihydroxy-3-phenylpropionate, the C13 side chain of paclitaxel, from ethyl cinnamate.
合成了两种可回收利用的小分子配体,并在两种不同体系的Sharpless不对称二羟化反应中用于催化肉桂酸乙酯,以合成紫杉醇的重要中间体(2R,3S)-2,3-二羟基-3-苯丙酸乙酯。
3) Sharpless' asymmetric dihydroxylation
sharpless不对称双羟化
1.
Methods Sharpless′ asymmetric dihydroxylation was employed to construct the 3-hydroxychroman.
方法 运用sharpless不对称双羟化构筑手性的 3 羟基苯并二氢吡喃。
4) asymmetric dihydroxylation
不对称双羟化反应
1.
Synthesis of quinine and cinchonine derivatives and their catalytic performance in asymmetric dihydroxylation;
奎宁和辛可宁衍生物的合成及其在不对称双羟化反应中的催化作用
2.
Application of the ligand-OsO_4 in the asymmetric dihydroxylation reaction of several olefins afforded corresponding chiral diols in yield of 91%～94% and 93% e.
OsO4-2用于催化烯烃的不对称双羟化反应,化学产率91%~94%,e。
3.
METHODS The C13 side chain of the taxol was synthesized via asymmetric dihydroxylation of trans-cinnamate,which was catalyzed by a kind of free recoverable and resued chiral ligand and OsO4.
方法在可回收非支载型手性配体的催化作用下,通过不对称双羟化反应合成紫杉醇C13侧链,对侧链的羟基和氨基进行保护后生成(4S,5R)-N-苯甲酰基-2-(4′-甲氧基)苯基-4-苯基-1,3-氧氮杂戊环-5-甲酸,进而和7-三乙基硅烷巴卡亭-Ⅲ缩合、去保护获得紫杉醇。
5) asymmetric dihydroxylation(AD)
不对称双羟化反应(AD)
6) asymmetric dihydroxylation
不对称双羟基化反应
1.
N,N'-Diferrocenylmethyl-(1S,2S)-1,2-diphenylethanediamine was synthesized by two steps from (1S,2S)-1,2-diphenylethanediamine and ferrocenealdehyde, and has been used as chiral ligand to asymmetric dihydroxylation of olefins.
(1S,2S)-1,2-二苯基乙二胺和甲酰基二茂铁经缩合和还原两步反应,以90%的产率合成了N,N'-二茂铁甲基-(1S,2S)-1,2-二苯基乙二胺,并以其为配体催化烯烃的不对称双羟基化反应,获得了较高的对映选择性(71%～86%ee)。
补充资料：双二乙二醇基化钛化双-2,4-戊烷二酯
CAS：84788-13-6
中文名称：双二乙二醇基化钛化双-2,4-戊烷二酯
英文名称：bis(Diethyleneglycoxy)titanium bis(2,4-Pentanedionate)
中文名称：双二乙二醇基化钛化双-2,4-戊烷二酯
英文名称：bis(Diethyleneglycoxy)titanium bis(2,4-Pentanedionate)
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