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Results: 1-10 |
Results: 10
First enantioselective total synthesis of glutinone and its C(7) and C(11)epimers
Authors: Zhang, Z Xiong, ZM Zheng, GJ Li, YL
Citation: Z. Zhang et al., First enantioselective total synthesis of glutinone and its C(7) and C(11)epimers, TETRAHEDR-A, 12(15), 2001, pp. 2137-2141
Enantioselective total synthesis of eudesma-3,11(13)-dien-12-oic acid
Authors: Chen, YG Zhou, G Liu, LJ Xiong, ZM Li, YL
Citation: Yg. Chen et al., Enantioselective total synthesis of eudesma-3,11(13)-dien-12-oic acid, SYNTHESIS-S, (9), 2001, pp. 1305-1307
First enantioselective total syntheses and absolute configurations of 4,5-dioxo-seco-gamma-eudesmol and 5 beta,11-dihydroxyiphionan-4-one, two aglycones of naturally occurring sesquiterpenes with new skeletons
Authors: Gao, XL Xiong, ZM Zhou, G Li, YL
Citation: Xl. Gao et al., First enantioselective total syntheses and absolute configurations of 4,5-dioxo-seco-gamma-eudesmol and 5 beta,11-dihydroxyiphionan-4-one, two aglycones of naturally occurring sesquiterpenes with new skeletons, SYNTHESIS-S, (1), 2001, pp. 37-39
An efficient synthetic strategy for introduction of C-3-C-4 double bond into eudesmane skeleton: First total synthesis of (+)-chrysanthemol
Authors: Chen, YG Zhou, G Xiong, ZM Liu, LJ Li, YL
Citation: Yg. Chen et al., An efficient synthetic strategy for introduction of C-3-C-4 double bond into eudesmane skeleton: First total synthesis of (+)-chrysanthemol, J CHIN CHEM, 48(2), 2001, pp. 261-264
Simple enantioselective total synthesis of glabrescol, a chiral C-2-symmetric pentacyclic oxasqualenoid
Authors: Xiong, ZM Corey, EJ
Citation: Zm. Xiong et Ej. Corey, Simple enantioselective total synthesis of glabrescol, a chiral C-2-symmetric pentacyclic oxasqualenoid, J AM CHEM S, 122(38), 2000, pp. 9328-9329
Simple total synthesis of the pentacyclic C-s-symmetric structure attributed to the squalenoid glabrescol and three C-s-symmetric diastereomers compel structural revision
Authors: Xiong, ZM Corey, EJ
Citation: Zm. Xiong et Ej. Corey, Simple total synthesis of the pentacyclic C-s-symmetric structure attributed to the squalenoid glabrescol and three C-s-symmetric diastereomers compel structural revision, J AM CHEM S, 122(19), 2000, pp. 4831-4832
A facile synthesis of 3-oxo-7 alpha H-eudesma-4-en-9 beta, 12-diol
Authors: Liu, LJ Zhou, G Li, J Chen, YG Xiong, ZM Li, YL
Citation: Lj. Liu et al., A facile synthesis of 3-oxo-7 alpha H-eudesma-4-en-9 beta, 12-diol, SYN COMMUN, 29(19), 1999, pp. 3379-3384
An exceptionally short and simple enantioselective total synthesis of pentacyclic triterpenes of the beta-amyrin family
Authors: Huang, AX Xiong, ZM Corey, EJ
Citation: Ax. Huang et al., An exceptionally short and simple enantioselective total synthesis of pentacyclic triterpenes of the beta-amyrin family, J AM CHEM S, 121(43), 1999, pp. 9999-10003
First synthesis of (+)-5 alpha-hydroxy-beta-selinene and (-)-5 beta-hydroxy-beta-selinene
Authors: Xiong, ZM Zhou, G Chen, YG Li, YL
Citation: Zm. Xiong et al., First synthesis of (+)-5 alpha-hydroxy-beta-selinene and (-)-5 beta-hydroxy-beta-selinene, J CHEM R-S, (8), 1998, pp. 450-451
Facile synthesis of 6 beta-hydroxy-(7 alpha H)-eudesm-4-en-3-one and beta-cyperone
Authors: Zhou, G Xiong, ZM Chen, YG Li, YL
Citation: G. Zhou et al., Facile synthesis of 6 beta-hydroxy-(7 alpha H)-eudesm-4-en-3-one and beta-cyperone, J CHEM R-S, (10), 1998, pp. 650-651
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