中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Facile Stereoselective Synthesis of Fluorinated Flavanone Derivatives via a One-Pot Tandem Reaction

文献类型:期刊论文

作者Cui HF(崔海峰) ; Li P(李鹏) ; Chai Z(柴卓) ; Zheng CW(郑昌武) ; Zhao G(赵刚) ; Zhu SZ(朱仕正)
刊名J. Org. Chem.
出版日期2009
卷号74期号:3页码:1400-1402
ISSN号0022-3263
其他题名一锅法立体选择性合成含氟黄酮
通讯作者赵刚 ; 朱仕正
英文摘要A series of fluorinated flavanones were synthesized in moderate to good yields with excellent diastereoselectivities under mild reaction conditions via a one-pot tandem procedure involving a proline-catalyzed Knoevenagel condensation, a Michael addition, and an electrophilic fluorination by NFSI.
学科主题有机氟化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/jo8023818
语种英语
WOS记录号WOS:000263004300067
公开日期2013-01-18
源URL[http://202.127.28.38/handle/331003/14472]  
专题上海有机化学研究所_中科院有机氟化学重点实验室
推荐引用方式
GB/T 7714
Cui HF,Li P,Chai Z,et al. Facile Stereoselective Synthesis of Fluorinated Flavanone Derivatives via a One-Pot Tandem Reaction[J]. J. Org. Chem.,2009,74(3):1400-1402.
APA 崔海峰,李鹏,柴卓,郑昌武,赵刚,&朱仕正.(2009).Facile Stereoselective Synthesis of Fluorinated Flavanone Derivatives via a One-Pot Tandem Reaction.J. Org. Chem.,74(3),1400-1402.
MLA 崔海峰,et al."Facile Stereoselective Synthesis of Fluorinated Flavanone Derivatives via a One-Pot Tandem Reaction".J. Org. Chem. 74.3(2009):1400-1402.

入库方式: OAI收割

来源:上海有机化学研究所

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