期刊
TETRAHEDRON
卷 64, 期 51, 页码 11568-11579出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2008.10.032
关键词
Martinelline; Martinellic acid; Tandem Michael-aldol reaction; Organocatalyst; Asymmetric synthesis
资金
- Ministry of Education, Culture, Sports, Science and Technology, Japan
The martinelline chiral core 3 and its disastereomer were synthesized by using the asymmetric tandem Michael-aldol reaction as the key step from 4-methyoxycarbonylanthranilaldehyde and the alpha,beta-unsatuarated aldehyde (C) 2008 Published by Elsevier Ltd.
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