HOME PAGE
Zhenlei Song
RESEARCH
PUBLICATIONS
MEMBERS
Team
Current Members
Former Members
PICTURES
中文版
PUBLICATIONS
7. A General Efficient Strategy for cis-3a-Aryloctahydroindole Alkaloids via Stereocontrolled ZnBr2-Catalyzed Rearrangement of 2,3-Aziridino Alcohols.
Song, Z L ; Wang, B M ; Tu, Y Q ; Fan, C A ; Zhang, S Y Org Lett 2003, 5, 2319-2321
6. Halogen Cation Induced Stereoselective Semipinacol-Type Rearrangement of Allylic Alcohols: A Highly Efficient Approach to α-Quaternary β-Haloketo Compounds.
Wang, B ; Song, Z L ; Fan, C ; Tu, Y ; Chen, W Synlett 2003, 1497-1499
5. Progressive Studies on the Novel Samarium-Catalyzed Diastereoselective Tandem Semipinacol Rearrangement/Tishchenko Reduction of Secondary α-Hydroxy Epoxides.
Fan, C ; Hu, X ; Tu, Y ; Wang, B ; Song, Z L Chem Eur J 2003, 9, 4301-4310
4. Lewis Acid Promoted Highly Stereoselective Rearrangement of 2,3-Aziridino Alcohols: A New Efficient Approach to β-Amino Carbonyl Compounds.
Wang, B ; Song, Z L ; Fan, C ; Tu, Y ; Shi, Y Org Lett 2002, 4, 363-366
3. Samarium-Catalyzed Tandem Semipinacol Rearrangement/Tishchenko Reaction of α-Hydroxy Epoxides: A Novel Approach to Highly Stereoselective Construction of 2-Quaternary 1,3-Diol Units.
Fan, C ; Wang, B ; Tu, Y ; Song, Z L Angew Chem Int Ed 2001, 40, 3877-3880
2. A New One-Pot Synthesis of 2-Quaternary 1,3-Diketones.
Ren, S ; Wang, F ; Dou, H ; Fan, C ; He, L ; Song, Z L ; Xia, W ; Li, D ; Jia, Y ; Li, X ; Tu, Y Syntheses 2001, 16, 2384-2388
1.Sm(III)-Catalyzed Highly Diastereoselective Rearrangement and Reduction of α-Hydroxy Epoxides. A New Synthetic Method for Preparing 1,3-Diol Monoesters.
Fan, C ; Song, Z L ; Tu, Y ; Wang, B Chinese J Org Chem 2001, 21, 1074-1080
97 items
Previous
1
2
3
4
5
6
7
8
9
10
Next
E-mail: zhenleisong@scu.edu.cn
Adress: No.17 People's South Road, Chengdu
Tel: 028-85501876