1.
A Novel Process for Stereoselective Synthesis of α-Asarone;
立体选择性合成α-细辛脑的工艺研究
2.
Highly Demensional Selective Composition of E-alkene Aromatic Sulfur and Ether;
E-烯基芳基硫醚的高立体选择性合成
3.
Study on Diastereoselective Synthesis of Chiral M Receptor Antagonists;
M受体手性拮抗剂的立体选择性合成研究
4.
Stereoselective Synthesis of Glycosides by Phase-Transition Catalysis;
相转移催化法立体选择性合成糖苷类化合物
5.
Regio-and Stereo-selective Synthesis of Novel Spirooxindole Compounds
区域和立体选择性合成新型螺羟吲哚类化合物
6.
The stereoselective synthesis and primary activity assay of Bestatin′s derivatives
Bestatin衍生物的立体选择性合成及活性研究
7.
Study on the Highly Stereoselective Synthesis of 1-Aminocyclopropane-1-carboxylic Acid Derivatives;
环丙烷氨基酸衍生物的高立体选择性合成研究
8.
Stereoselective Synthesis of β-Bromostyrene Derivatives and Its Applications;
β-卤代烯烃衍生物的立体选择性合成及应用
9.
Highly Stereoselective Synthesis of E-4, 5-Disubstituted-2-Pyrrorlidinones;
E-4,5-二苯基-2-吡咯烷酮的高立体选择性合成
10.
Recent development on the stereoselective synthesis of E-and Z-β-arylvinyl bromides
E-和Z-β-溴代芳乙烯的立体选择性合成进展
11.
Synthesis of Phenylpropanoid Glycoside Luteoside A and Stereoselective Synthesis of β-Lactams;
苯丙素苷Luteoside A的合成和β-内酰胺的立体选择性合成
12.
Catalytic Stereoselective Synthesis of Relative Organofluorine Compounds
催化立体选择性合成含氟有机化合物的反应研究
13.
Study on the Stereoselective Synthesis of 2,3-Disubstituted 1-Aminocyclopropane-1-carboxylic Acid Derivatives;
2，3-二取代环丙烷氨基酸衍生物的立体选择性合成研究
14.
Catalytic Stereoselective Synthesis of Fluorine-containing 1-Indanone Derivatives via Tandem Nazarov Cyclization and Electrophilic Fluorination;
催化串联Nazarov环化/亲电氟化反应—立体选择性合成含氟1-茚酮衍生物
15.
Cesium Base Promoted Synthesis of Alkynyl Selenides(Tellurides) and Stereoselective Synthesis Bissubstituted Vinyl Sulfides;
铯碱作用下炔硒（碲）醚的制备及二取代芳硫烯的立体选择性合成
16.
Stereoselective Synthesis of Novel 3-C-branched Ribofuranose Derivatives
新型3-C-支链呋喃核糖衍生物的立体选择性合成
17.
Study on the Synthesis of 1, 5-Benzodiazepines and Steroeselective Synthesis of Heterocyclic α-Amino Phosphonates Catalyzed by Lanthanide Compounds;
稀土化合物催化合成1，5-苯并二氮杂卓及立体选择性合成杂环α-氨基膦酸酯的研究
18.
Stereoselective and Enantioselective Synthesis of Trans-2, 5-disubstituted Tetrahydrofurans
反式-2，5-二取代四氢呋喃的立体选择性和对映选择性合成