The Reaction of N-Methyl-1,2,4-triazoline-3,5-dione with Tetracyclopropylethylene. Formation of an Unusual Meso-ionic Product and Its Rearrangement to the Diazetidine-Reference-Cited by-同舟云学术

The Reaction of N-Methyl-1,2,4-triazoline-3,5-dione with Tetracyclopropylethylene. Formation of an Unusual Meso-ionic Product and Its Rearrangement to the Diazetidine

Published:2003-12-25 Issue:3 Volume:126 Page:700-701
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Kim Duk Kyung¹,O'Shea Kevin E.¹

Affiliation:

1. Department of Chemistry, Florida International University, University Park, Miami, Florida 33199

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja038359l

Reference16 articles.

1. Reaction of electrophiles with unsaturated systems: triazolinedione-olefin reactions

2. Mechanism of Ene Reactions of Singlet Oxygen. A Two-Step No-Intermediate Mechanism

3. A New Form of Kinetic Isotope Effect. Dynamic Effects on Isotopic Selectivity and Regioselectivity

4. Intramolecular and Intermolecular Kinetic Isotope Effects (KIE) in the Nitrosoarene Ene Reaction: Experimental Evidence for Reversible Intermediate Formation

5. The Ene Reactions of Nitroso Compounds Involve Polarized Diradical Intermediates

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