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13. Strategies and Approaches for Constructing 1-Oxadecalins.
Antoline, J E ; Hsung, R P ; Huang, J ; Song, Z L ; Li, G Org Lett 2007, 9, 1275-1278
12. Studies on Wagner-Meerwein Rearrangement of Benzospirocyclic β-Bromo Ketones and Application to Formal Synthesis of (±)-Colchicine
Wang, A ; Song, Z L ; Gao, S ; Jiang, Y ; Yuan, D ; Tu, Y ; Li, N Chinese J Org Chem 2007, 27, 1171-1175
11. Synthetically Useful Wagner-Meerwein Rearrangement of α-Quaternary Bromovinyl Methyl Ethers.
Wang, A ; Tu, Y ; Song, Z L ; Yuan, D ; Hu, X ; Wang, S ; Gao, S Eur J Org Chem 2006, 2691-2694
10. Studies on The Synthesis of Morphinan Alkaloid: Preparation of The Key Allylic Silyl Ether Precursor.
Song, Z L ; Tu, Y ; Gao, S ; Jiang, Y ; Zhang, S Chinese Chem Lett 2005, 1445-1447
9. A General and Efficient Strategy for 7-Aryloctahydroindole and cis-3a-Aryloctahydroindole Alkaloids: Total Syntheses of (±)-Lycorane and (±)-Crinane.
Gao, S ; Tu, Y ; Song, Z L ; Wang, A ; Fan, X ; Jiang, Y J Org Chem 2005, 70, 6523-6525
8. An Efficient Total Synthesis of (±)-Lycoramine.
Fan, C A ; Tu, Y Q ; Song, Z L ; Zhang, E ; Shi, L ; Wang, M ; Wang, B M ; Zhang, S Y Org Lett 2004, 6, 4691-4694
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
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