Issue 3, 1996
From the journal:

Chemical Communications

An unusual thermodynamic preference of chiral N-arylsulfonyl cis-3-alkyl-2-vinylaziridines over their trans-isomers: palladium(0)-catalysed equilibration reactions

Norio Mimura,   Toshiro Ibuka,   Masako Akaji,   Yoshihisa Miwa,   Tooru Taga,   Kazuo Nakai,   Hirokazu Tamamura,   Nobutaka Fujii  and  Yoshinori Yamamoto  

Abstract

Palladium (0)-catalysed reactions of N-alkylsulfonyl- or N-arylsulfonyl-3-alkyl-2-vinyfaziridines reveal that 2,3-cis-isomers are more stable than the corresponding 2,3-trans-isomers in accord with ab initio calculations.

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Article information

DOI
https://doi.org/10.1039/CC9960000351
Article type
Paper

Chem. Commun., 1996, 351-352

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An unusual thermodynamic preference of chiral N-arylsulfonyl cis-3-alkyl-2-vinylaziridines over their trans-isomers: palladium(0)-catalysed equilibration reactions

N. Mimura, T. Ibuka, M. Akaji, Y. Miwa, T. Taga, K. Nakai, H. Tamamura, N. Fujii and Y. Yamamoto, Chem. Commun., 1996, 351 DOI: 10.1039/CC9960000351

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