Stereo-, Regio-, and Chemoselective [3+2]-Cycloaddition of (2E,4E)-Ethyl 5-(Phenylsulfonyl)penta-2,4-dienoate with Various Azomethine Ylides, Nitrones, and Nitrile Oxides: Synthesis of Pyrrolidine, Isoxazolidine, and Isoxazoline Derivatives and a Computational Study

被引:21
作者
Sankar, Ulaganathan [1 ]
Kumar, Ch. Venkata Surya [2 ]
Subramanian, V. [2 ]
Balasubramanian, K. K. [3 ]
Mahalakshimi, S. [1 ]
机构
[1] Univ Madras, Dept Chem, Pachaiyappas Coll, Madras 600030, Tamil Nadu, India
[2] CSIR Cent Leather Res Inst, Chem Lab, Madras 600020, Tamil Nadu, India
[3] Indian Inst Technol, Dept Chem, Madras 600020, Tamil Nadu, India
关键词
1,3-DIPOLAR CYCLOADDITION; STEREOSELECTIVE-SYNTHESIS; REACTIVITY; REGIOSELECTIVITY; CONSTRUCTION; 1,3-DIENES; SULFONES; AMINES; ROUTE; ACID;
D O I
10.1021/acs.joc.5b02845
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
One-pot chemo-, regio-, and stereoselective synthesis of series of heterocyclic and spiroheterocyclic compounds was accomplished through mono- and bis[3 + 2]-cycloaddition reactions of (2E,4E)-ethyl 5-(phenylsulfonyl)penta-2,4-dienoate as a dipolarophile with azomethine ylides, nitrones, and nitrile oxides in good yields. The structures of the products were established by spectroscopic techniques as well as by single-crystal MUD study, and DFT calculations were performed to further understand the mechanism of this [3 + 2]-cycloaddition reaction.
引用
收藏
页码:2340 / 2354
页数:15
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