An unusually strict product partition of an excited diazirine–carbene system
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1993/C3/C39930001597
Reference14 articles.
1. Photolysis of 3-chlorodiazirine in the presence of alkenes. Kinetic evidence for intervention of a carbene-alkene intermediate in addition of chlorocarbene to alkene
2. Energy barrier for 1,2-hydrogen migration in benzylchlorocarbene
3. Thermolysis and photolysis of 3-chloro-3-benzyldiazirines in alkenes; evidence for a carbene-alkene complex
4. Photolysis of alkylhalodiazirines: Two pathways for vinyl halide formation
5. Concurrent hydrogen migration and nitrogen extrusion in the excited states of alkylchlorodiazirines
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