中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Unusual fluoroalkenylation of porphyrins: A highly stereoselective synthesis of 10,20-diaryl-5-[(E)-fluoroalkenyl]-15-(fluoroalkyl)porphyrins cyclization

文献类型:期刊论文

作者Jin LM(金利美) ; Yin JJ(尹娟娟) ; Chen L(陈亮) ; Xiao JC(肖吉昌) ; Guo CC(郭灿城) ; Chen QY(陈庆云)
刊名Eur. J. Org. Chem.
出版日期2006
期号15页码:3405-3411
ISSN号1434-193X
其他题名不同寻常的卟啉氟烷基化: 高度立体选择性地合成10,20-二芳基-5-[(E)-氟烯基]-15-氟烷基卟啉
通讯作者郭灿城 ; 陈庆云
英文摘要A series of 10,20-diaryl-5-[(E)-fluoroalkenyl]-15-(fluoroalkyl)porphyrins has been synthesized by the reaction of free-base 5,15-diarylporphyrins with fluoroalkyl iodides in the presence of Na2S2O4. Subsequent intramolecular cyclization of the corresponding (fluoroalkenyl)porphyrins occurs smoothly in refluxing toluene/H2O. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)
学科主题有机氟化学
收录类别SCI
原文出处http://dx.doi.org/10.1002/ejoc.200600130
语种英语
公开日期2013-01-17
源URL[http://202.127.28.38/handle/331003/13620]  
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
Jin LM,Yin JJ,Chen L,et al. Unusual fluoroalkenylation of porphyrins: A highly stereoselective synthesis of 10,20-diaryl-5-[(E)-fluoroalkenyl]-15-(fluoroalkyl)porphyrins cyclization[J]. Eur. J. Org. Chem.,2006(15):3405-3411.
APA 金利美,尹娟娟,陈亮,肖吉昌,郭灿城,&陈庆云.(2006).Unusual fluoroalkenylation of porphyrins: A highly stereoselective synthesis of 10,20-diaryl-5-[(E)-fluoroalkenyl]-15-(fluoroalkyl)porphyrins cyclization.Eur. J. Org. Chem.(15),3405-3411.
MLA 金利美,et al."Unusual fluoroalkenylation of porphyrins: A highly stereoselective synthesis of 10,20-diaryl-5-[(E)-fluoroalkenyl]-15-(fluoroalkyl)porphyrins cyclization".Eur. J. Org. Chem. .15(2006):3405-3411.

入库方式: OAI收割

来源:上海有机化学研究所

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