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Chirality based on pillar[n]arenes and its complexes Journal article
Diao, Kai, Ruan, Chao, Wang, Ranran, Li, Shengke, Jiang, Juli, Wang, Leyong. Chirality based on pillar[n]arenes and its complexes[J]. Tetrahedron Letters, 2024, 137, 154941.
Authors:  Diao, Kai;  Ruan, Chao;  Wang, Ranran;  Li, Shengke;  Jiang, Juli; et al.
Favorite | TC[WOS]:2 TC[Scopus]:2  IF:1.5/1.6 | Submit date：2024/04/02
Circularly Polarized Luminescence  Macrocycles  Pillar[n]Arenes  Supramolecular Chirality  
Meloslines A and B, two novel indole alkaloids from Alstonia scholaris Journal article
Kuok, Chiu-Fai, Zhang, Jian, Fan, Chun-Lin, Zhang, Qing-Wen, Fan, Run-Zhu, Zhang, Dong-Mei, Zhang, Xiao-Qi, Ye, Wen-Cai. Meloslines A and B, two novel indole alkaloids from Alstonia scholaris[J]. TETRAHEDRON LETTERS, 2017, 58(28), 2740-2742.
Authors:  Kuok, Chiu-Fai;  Zhang, Jian;  Fan, Chun-Lin;  Zhang, Qing-Wen;  Fan, Run-Zhu; et al.
Favorite | TC[WOS]:15 TC[Scopus]:21  IF:1.5/1.6 | Submit date：2018/10/30
Indole Alkaloids  Alstonia Scholaris  Absolute Configuration  Cytotoxicity  
Ytterbium(III) triflate catalyzed annulation of propargylic 1,4-diols with aryl sulfonamides to give highly substituted pyrrole derivatives Journal article
Zhang X., Teo J.W., Ma D.-L., Leung C.-H., Chan P.W.H.. Ytterbium(III) triflate catalyzed annulation of propargylic 1,4-diols with aryl sulfonamides to give highly substituted pyrrole derivatives[J]. Tetrahedron Letters, 2014, 55(49), 6703-6707.
Authors:  Zhang X.;  Teo J.W.;  Ma D.-L.;  Leung C.-H.;  Chan P.W.H.
Favorite | TC[WOS]:16 TC[Scopus]:16 | Submit date：2018/11/06
Homogeneous Catalysis  Propargylic 1,4-diols  Pyrroles  Tandem Reactions  Ytterbium(Iii) Triflate  
Synthesis of highly substituted indene derivatives by Brønsted acid catalyzed Friedel-Crafts reaction of homoallylic alcohols Journal article
Zhang X., Teo W.T., Rao W., Ma D.-L., Leung C.-H., Chan P.W.H.. Synthesis of highly substituted indene derivatives by Brønsted acid catalyzed Friedel-Crafts reaction of homoallylic alcohols[J]. Tetrahedron Letters, 2014, 55(29), 3881-3884.
Authors:  Zhang X.;  Teo W.T.;  Rao W.;  Ma D.-L.;  Leung C.-H.; et al.
Favorite | TC[WOS]:23 TC[Scopus]:23 | Submit date：2018/11/06
Brønsted Acid  Friedel-crafts Reaction  Homoallylic Alcohols  Homogeneous Catalysis  Indene Derivatives  
Ervahainine A, a new cyano-substituted oxindole alkaloid from Ervatamia hainanensis Journal article
Liu Z.-W., Yang T.-T., Wang W.-J., Li G.-Q., Tang B.-Q., Zhang Q.-W., Fan C.-L., Zhang D.-M., Zhang X.-Q., Ye W.-C.. Ervahainine A, a new cyano-substituted oxindole alkaloid from Ervatamia hainanensis[J]. Tetrahedron Letters, 2013, 54(48), 6498-6500.
Authors:  Liu Z.-W.;  Yang T.-T.;  Wang W.-J.;  Li G.-Q.;  Tang B.-Q.; et al.
Favorite | TC[WOS]:20 TC[Scopus]:24  IF:1.5/1.6 | Submit date：2018/12/28
Apocynaceae  Ervatamia Hainanensis  Indole Alkaloid  
Synthesis of functionalized siloles from Si-tethered diynes Journal article
Luo Q., Gu L., Wang C., Liu J., Zhang W., Xi Z.. Synthesis of functionalized siloles from Si-tethered diynes[J]. Tetrahedron Letters, 2009, 50(26), 3213-3215.
Authors:  Luo Q.;  Gu L.;  Wang C.;  Liu J.;  Zhang W.; et al.
Favorite | TC[WOS]:13 TC[Scopus]:14 | Submit date：2018/12/18
1,4-diiodo-1,3-butadiene  1,4-dilithio-1,3-butadiene  Cleavage Of Si-c Bond  Phenyl-bridged Bis-silole  Si-tethered Diynes  Silole  Zirconacyclopetadiene  
Cochinchistemonine, an unprecedented skeleton alkaloid from Stemona cochinchinensis Journal article
Lin, L., Tang, C., Dien, P., Xu, R., Ye, Y.. Cochinchistemonine, an unprecedented skeleton alkaloid from Stemona cochinchinensis[J]. Tetrahedron Letters, 2007, 1559-1561.
Authors:  Lin, L.;  Tang, C.;  Dien, P.;  Xu, R.;  Ye, Y.
Favorite |   IF:1.5/1.6 | Submit date：2022/07/27
Stemona cochinchinensis  Stemonaceae  Cochinchistemonine-type alkaloid  Cochinchistemonine  
The allomorphism of a photochromic diarylethene Journal article
Pu S.-Z., Zhang F.-S., Sun F., Wang R.-J., Zhou X.-H., Chan S.-K.. The allomorphism of a photochromic diarylethene[J]. Tetrahedron Letters, 2003, 44(5), 1011.
Authors:  Pu S.-Z.;  Zhang F.-S.;  Sun F.;  Wang R.-J.;  Zhou X.-H.; et al.
Favorite | TC[WOS]:38 TC[Scopus]:43 | Submit date：2018/10/30
Allomorphism  Diarylethene  Photochromic  X-ray Crystallographic Analysis