Enantioselective approach to 13a-methylphenanthroindolizidine alkaloids.
Summary of "Enantioselective approach to 13a-methylphenanthroindolizidine alkaloids."
The first enantioselective approach to 13a-methylphenanthroindolizidine alkaloids is reported, featuring an efficient stereoselective Seebach's alkylation and Pictet-Spengler cyclization. The proposed and other three most probable structures were ruled out, indicating hypoestestatin 1 needs further assignment.
State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, Nankai University , Tianjin 300071, People's Republic of China.
This article was published in the following journal.
Name: The Journal of organic chemistry
Medical and Biotech [MESH] Definitions
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