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pro vyhledávání: '"Jia-Nan Mo"'
The Asymmetric A3(Aldehyde–Alkyne–Amine) Coupling: Highly Enantioselective Access to Propargylamines
Publikováno v:
Molecules, Vol 24, Iss 7, p 1216 (2019)
The recent developments in asymmetric A3 (aldehyde–alkyne–amine) coupling has been summarized in this review. Several interesting modifications of the ligands enabled the highly enantioselective synthesis of chiral propargylamines, which are furt
Externí odkaz:
https://doaj.org/article/8cee17fec5954aa3b0b65f5439aca762
Publikováno v:
Organic Letters. 24:6247-6251
Publikováno v:
Tetrahedron Letters. 121:154483
Autor:
Junqi Su, Jia‐Nan Mo, Xiangyang Chen, Alexander Umanzor, Zheng Zhang, Kendall N. Houk, Jiannan Zhao
Publikováno v:
Angewandte Chemie International Edition. 61
Autor:
Junqi Su, Jia‐Nan Mo, Xiangyang Chen, Alexander Umanzor, Zheng Zhang, Kendall N. Houk, Jiannan Zhao
Publikováno v:
Angewandte Chemie. 134
Autor:
Xiangyang Chen, Jia-Nan Mo, Zheng Zhang, Junqi Su, Kendall N. Houk, Jiannan Zhao, Alexander Umanzor
Publikováno v:
Angewandte Chemie (International ed. in English). 61(5)
Phosphine mediated deoxygenative nucleophilic substitutions, such as the Mitsunobu reaction, are of great importance in organic synthesis. However, the conventional protocols require stoichiometric oxidants to trigger the formation of the oxyphosphon
The Asymmetric A3(Aldehyde–Alkyne–Amine) Coupling: Highly Enantioselective Access to Propargylamines
Publikováno v:
Molecules, Vol 24, Iss 7, p 1216 (2019)
The recent developments in asymmetric A3 (aldehyde–alkyne–amine) coupling has been summarized in this review. Several interesting modifications of the ligands enabled the highly enantioselective synthesis of chiral propargylamines, which are furt
The Asymmetric A³(Aldehyde⁻Alkyne⁻Amine) Coupling: Highly Enantioselective Access to Propargylamines
Publikováno v:
Molecules
The recent developments in asymmetric A3 (aldehyde–alkyne–amine) coupling has been summarized in this review. Several interesting modifications of the ligands enabled the highly enantioselective synthesis of chiral propargylamines, which are furt
Publikováno v:
The Journal of organic chemistry. 83(1)
The decarbonylation of primary, secondary, and tertiary alkyl-substituted acyl radicals has been investigated through photoredox catalysis. A series of quaternary carbons and γ-ketoesters have been directly constructed by the photoredox 1,4-conjugat
Publikováno v:
Journal of Organic Chemistry; 1/5/2018, Vol. 83 Issue 1, p253-259, 7p