中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Enantioselective synthesis of(+)-laburnine and(-)-isoretronecanol by L-prolinecatalyzed self-aldol reaction

文献类型:期刊论文

作者Ma Shichao2; Cao Sufeng2; Mei Desheng1; Duan Wenhu2
刊名West China Journal of Pharmaceutical Sciences
出版日期2015
卷号30期号:2页码:167-171
关键词(+) laburnine (-)-isoretronecanol Self-aldol reaction Organocatalysis Proline (+) Laburnine (-)-isoretronecanol Enantioselective synthesis
ISSN号1006-0103
其他题名L-脯氨酸催化的(+)-laburnine和(-)-isoretronecanol的不对称合成
文献子类Article
英文摘要OBJECTIVE To explore a novel,effective and concise enantioselective approach to the synthesis of(+)-laburnine and(-)-isoretronecanol. METHODS The chiral center was constructed by L-porline promoted self-aldol reaction with known compounds initial materials. A number of transformations including reduction,protection,tosylation,nucleophilic substitution,hydrolysis,mesylation,reuctive cyclization and deprotection were involved in this approach. RESULTS(+)-laburnine and(-)-isoretronecanol were synthesized by eight steps. CONCLUSION The total yield is 27% and 8%,respectively.
WOS研究方向Pharmacology & Pharmacy (provided by Clarivate Analytics)
语种中文
CSCD记录号CSCD:5404752
源URL[http://119.78.100.183/handle/2S10ELR8/269286]  
专题药物化学研究室
通讯作者Duan Wenhu
作者单位1.Shanghai Institute of Materia Medica,Chinese Academy of Sciences, Shanghai 201203, China.
2.School of Pharmacy,East China University of Science and Technology, Shanghai 200237, China.;
推荐引用方式
GB/T 7714
Ma Shichao,Cao Sufeng,Mei Desheng,et al. Enantioselective synthesis of(+)-laburnine and(-)-isoretronecanol by L-prolinecatalyzed self-aldol reaction[J]. West China Journal of Pharmaceutical Sciences,2015,30(2):167-171.
APA Ma Shichao,Cao Sufeng,Mei Desheng,&Duan Wenhu.(2015).Enantioselective synthesis of(+)-laburnine and(-)-isoretronecanol by L-prolinecatalyzed self-aldol reaction.West China Journal of Pharmaceutical Sciences,30(2),167-171.
MLA Ma Shichao,et al."Enantioselective synthesis of(+)-laburnine and(-)-isoretronecanol by L-prolinecatalyzed self-aldol reaction".West China Journal of Pharmaceutical Sciences 30.2(2015):167-171.

入库方式: OAI收割

来源:上海药物研究所

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