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.
Affiliation
State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, Nankai University , Tianjin 300071, People's Republic of China.
Journal Details
This article was published in the following journal.
Name: The Journal of organic chemistry
ISSN: 1520-6904
Pages: 7981-7
Links
- PubMed Source: http://www.ncbi.nlm.nih.gov/pubmed/22946502
- DOI: http://dx.doi.org/10.1021/jo3012122
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