Photolyses directes et sensibilisees d'homopyrazolenines et de bis Δ1-pyrazolines.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Multiple mechanisms in the thermal and photochemical decomposition of 2,3-diazabicyclo[3.1.0]hex-2-enes
2. Chemistry of bent bonds. XXXVI. Photolysis of substituted derivatives of 2,3-diazabicyclo[3.1.0]hex-2-ene. Simple route to certain bicyclo[1.1.0]butanes
3. Cyclopropènes électrophiles II (1). Réactions de cycloaddition 1,3 dipolaires.
4. Decomposition photochimique sensibilisee de pyrazolines. II. Synthese de dimethyl-5,5 bicyclo (2.1.0) pentanes
5. Doppelte 1,3-dipolare Addition an eine Dreifachbindung zum Bicyclo [1.1.0]butan-System
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1. Cycloadditions and condensations as essential tools in spiropyrazoline synthesis;European Journal of Medicinal Chemistry;2013-05
2. Substituent Effect on Reactivity of Triplet Excited State of 2,3-Diazabicyclo[2.2.1]hept-2-enes, DBH Derivatives: α C–N Bond Cleavage versus β C–C Bond Cleavage;The Journal of Organic Chemistry;2012-10-01
3. Photochemical ring contraction of 4-heteroaryl-substituted 1,4(or 3,4)-dihydropyrimidines into imidazoles;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
4. Synthesis and Structural Elucidation of Novel Spiropyrazolines Precursors to Spiro-gem-dimethylcyclopropanes;Journal of Chemical Research;2005-08
5. Competitive diradical and diazoalkane formation in the thermolysis and photolysis of the azoalkane 7,7,8-trimethyl-2,3-diazatricyclo[4.2.1.04,8 inon-2-ene;Tetrahedron Letters;1983-01
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