Cycloaddition of New N -Unsubstituted Azomethine Ylides Generated from N -(Trimethylsilylmethyl)thioureas to Electron-Deficient Olefins, Acetylenes and Aldehydes, Synthetic Equivalents of Nonstabilized Aminonitrile Ylides 1-Reference-Cited by-同舟云学术

Cycloaddition of New N -Unsubstituted Azomethine Ylides Generated from N -(Trimethylsilylmethyl)thioureas to Electron-Deficient Olefins, Acetylenes and Aldehydes, Synthetic Equivalents of Nonstabilized Aminonitrile Ylides 1

Published:2000-09 Issue:39 Volume:56 Page:7723-7735
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Tsuge Otohiko,Hatta Taizo,Tashiro Hideki,Kakura Yoshikazu,Maeda Hironori,Kakehi Akikazu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. (a) A part of this work has been published in preliminary form: Tsuge, O.; Hatta, T.; Kakura, Y.; Tashiro, H.; Maeda, H.; Kakehi, A. Chem. Lett.1997, 945.

2. (a) The desilylative route to azomethine ylides has been reviewed: (a) Vedejs, E.; West, F.G. Chem. Rev.1986, 86, 941.

3. (b) Terao, Y.; Aono, M.; Achiwa, K. Heterocycles1988, 27, 981.

4. WATER-INDUCED FORMATION OF AZOMETHINE YLIDE 1,3-DIPOLE. STEREOSPECIFIC AND REGIOSELECTIVE CYCLOADDITION REACTIONS

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