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Your search keyword '"Zeng-Liang Luo"' showing total 2 results
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2 results on '"Zeng-Liang Luo"'

1. Rh(II)-catalyzed intramolecular dearomatizing annulation of N-sulfonyl-1,2,3-triazoles: synthesis of polycyclic spiroindolines

Author

Li Chen, Qiang Kang, Pranjal P. Bora, and Zeng-Liang Luo

Subjects
Sulfonyl, chemistry.chemical_classification, Annulation, 010405 organic chemistry, Chemistry, Organic Chemistry, Enantioselective synthesis, 010402 general chemistry, 01 natural sciences, Biochemistry, 0104 chemical sciences, Catalysis, Intramolecular force, Yield (chemistry), Drug Discovery, Organic chemistry, Enantiomer
Abstract

An efficient approach for the synthesis of polycyclic spiroindolines has been developed by utilizing Rh(II)-catalyzed dearomatizing annulation of sulfonyl triazoles. An enantioselective variant of the process was also looked into briefly to achieve polycyclic spiroindolines in good yield with a promising 73.3: 26.7 enantiomeric ratio, demonstrating the potential for asymmetric catalysis.

Published
2016

2. ChemInform Abstract: Rh(II)-Catalyzed Intramolecular Dearomatizing Annulation of N-Sulfonyl-1,2,3-triazoles: Synthesis of Polycyclic Spiroindolines

Author

Li Chen, Qiang Kang, Zeng-Liang Luo, and Pranjal P. Bora

Subjects
Sulfonyl, chemistry.chemical_classification, Annulation, chemistry, Intramolecular force, Yield (chemistry), Enantioselective synthesis, General Medicine, Enantiomer, Combinatorial chemistry, Catalysis
Abstract

An efficient approach for the synthesis of polycyclic spiroindolines has been developed by utilizing Rh(II)-catalyzed dearomatizing annulation of sulfonyl triazoles. An enantioselective variant of the process was also looked into briefly to achieve polycyclic spiroindolines in good yield with a promising 73.3: 26.7 enantiomeric ratio, demonstrating the potential for asymmetric catalysis.

Published
2016

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