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Results: 1-9 |
Results: 9
Al-Hg promoted chemoselective dehalogenation of halohydrin aldol adducts
Authors: Wang, YC Yan, TH
Citation: Yc. Wang et Th. Yan, Al-Hg promoted chemoselective dehalogenation of halohydrin aldol adducts, CHEM COMMUN, (7), 2000, pp. 545-546
A facile method for the synthesis of enantiopure alpha-unsubstituted beta-hydroxy esters
Authors: Wang, YC Hwang, JY Chen, YC Chuang, SC Yan, TH
Citation: Yc. Wang et al., A facile method for the synthesis of enantiopure alpha-unsubstituted beta-hydroxy esters, TETRAHEDR-A, 11(8), 2000, pp. 1797-1800
Passive vibration control of space structure by receptance theory
Authors: Yan, TH Zheng, GT Huang, WH
Citation: Th. Yan et al., Passive vibration control of space structure by receptance theory, APP MATH ME, 21(4), 2000, pp. 471-478
A new approach for the chemoselective debromination of chiral bromohydrins. Toward the development of a very general approach to enantiopure alpha-unsubstituted beta-hydroxy acids
Authors: Wang, YC Yan, TH
Citation: Yc. Wang et Th. Yan, A new approach for the chemoselective debromination of chiral bromohydrins. Toward the development of a very general approach to enantiopure alpha-unsubstituted beta-hydroxy acids, J ORG CHEM, 65(20), 2000, pp. 6752-6755
DMAP-promoted racemization-free deacylation of carboxthioimide adducts: carboxthioimide as a versatile carboxy protecting group
Authors: Su, DW Wang, YC Yan, TH
Citation: Dw. Su et al., DMAP-promoted racemization-free deacylation of carboxthioimide adducts: carboxthioimide as a versatile carboxy protecting group, CHEM COMMUN, (6), 1999, pp. 545-546
An efficient method for the synthesis of enantiopure cis-alpha,beta-epoxy acids
Authors: Wang, YC Li, CL Tseng, HL Chuang, SC Yan, TH
Citation: Yc. Wang et al., An efficient method for the synthesis of enantiopure cis-alpha,beta-epoxy acids, TETRAHEDR-A, 10(17), 1999, pp. 3249-3251
A novel DMAP-promoted oxazolidinethione deacylation. Application for the direct conversion of the initial chiral thioimide aldols to various ester protecting groups.
Authors: Su, DW Wang, YC Yan, TH
Citation: Dw. Su et al., A novel DMAP-promoted oxazolidinethione deacylation. Application for the direct conversion of the initial chiral thioimide aldols to various ester protecting groups., TETRAHEDR L, 40(22), 1999, pp. 4197-4198
Asymmetric bromination-aldolization of chiral acetate titanium enolate derived from thioimide. A general approach to the synthesis of enantiopure alpha-bromo-beta-hydroxy carboxylic acids.
Authors: Wang, YC Su, DW Lin, CM Tseng, HL Li, CL Yan, TH
Citation: Yc. Wang et al., Asymmetric bromination-aldolization of chiral acetate titanium enolate derived from thioimide. A general approach to the synthesis of enantiopure alpha-bromo-beta-hydroxy carboxylic acids., TETRAHEDR L, 40(18), 1999, pp. 3577-3580
Toward the development of a general chiral alpha-substituted acetate enolate synthon for aldolization. DMAP- and NEt3-promoted oxazolidinethione "deacylation"
Authors: Wang, YC Su, DW Lin, CM Tseng, HL Li, CL Yan, TH
Citation: Yc. Wang et al., Toward the development of a general chiral alpha-substituted acetate enolate synthon for aldolization. DMAP- and NEt3-promoted oxazolidinethione "deacylation", J ORG CHEM, 64(17), 1999, pp. 6495-6498
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