Stereoselective formation of inverted housane in the denitrogenation of the diazenyl diradical photolytically derived from a stereolabeled diazabicyclo[2,2,1]hept-2-ene with bridgehead substituents as a function of solvent- and temperature-varied viscosity-Reference-Cited by-同舟云学术

Stereoselective formation of inverted housane in the denitrogenation of the diazenyl diradical photolytically derived from a stereolabeled diazabicyclo[2,2,1]hept-2-ene with bridgehead substituents as a function of solvent- and temperature-varied viscosity

Published:2001-05 Issue:1-2 Volume:340 Page:26-32
ISSN:0009-2614
Container-title:Chemical Physics Letters
language:en
Short-container-title:Chemical Physics Letters

Author:

Adam Waldemar,Martı́ Vicente,Sahin Coskun,Trofimov Alexei V.

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Reference25 articles.

1. Zur stereochemie der 1.2-cycloaddition an das bicyclo[2.1.0]system

2. Thermolysis of exo- and endo-5-methoxy-2,3-diazabicyclo[2.2.1]-2-heptene

3. Photodissociation of a bicyclic azoalkane: time-resolved coherent anti-Stokes Raman spectroscopy studies of vapor-phase 2,3-diazabicyclo[2.2.1]hept-2-ene

4. Dynamics of the thermal decomposition of 2,3-diazabicyclo[2.2.1]hept-2-ene

5. Photochemistry of the azoalkanes 2,3-diazabicyclo[2.2.1]hept-2-ene and spiro[cyclopropane-7,1'-[2,3]-diazabicyclo[2.2.1]hept-2-ene]: on the questions of one-bond vs. two-bond cleavage during the denitrogenation, cyclization vs. rearrangement of the 1,3-diradicals and double inversion

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1. Heavy-Atom Tunneling Processes during Denitrogenation of 2,3-Diazabicyclo[2.2.1]hept-2-ene and Ring Closure of Cyclopentane-1,3-diyl Diradical. Stereoselectivity in Tunneling and Matrix Effect;The Journal of Organic Chemistry;2020-06-12

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