Stereochemical Analysis of an Aromatic Triplet Di‐π‐methane Rearrangement
- 10 December 1986
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 69 (8) , 1936-1958
- https://doi.org/10.1002/hlca.19860690821
Abstract
No abstract availableKeywords
This publication has 76 references indexed in Scilit:
- A highly enantioselective synthesis of cyclopropane derivatives through chiral cobalt(II) complex catalyzed carbenoid reaction. General scope and factors determining the enantioselectivityJournal of the American Chemical Society, 1978
- Stereochemical and mechanistic aspects of the di-.pi.-methane rearrangement. Effect of structural constraints which preclude preferred modesJournal of the American Chemical Society, 1976
- Mechanistic and exploratory organic photochemistry. LXXXVIII. Stereochemistry at the methane carbon in the di-.pi.-methane rearrangementJournal of the American Chemical Society, 1974
- Di-.pi.-methane and oxa-di-.pi.-methane rearrangementsChemical Reviews, 1973
- Photochemistry of trans-1-phenyl-2-buteneJournal of the American Chemical Society, 1970
- Biradical mechanism in small ring compound reactionsThe Journal of Physical Chemistry, 1968
- Evidence for Trimethylenemethane as an Intermediate in a Pyrolysis ReactionJournal of the American Chemical Society, 1966
- Benzene- and Toluene-Photosensitized Isomerization of 1,2-Dimethylcyclopropane. The Triplet State of CyclopropaneJournal of the American Chemical Society, 1965
- Photoisomerization of Cyclopropane Derivatives. Photointerconversion of Propenes and CyclopropanesJournal of the American Chemical Society, 1965
- Cyclopropanes. VIII.1 Rates of Ring Opening of Substituted Cyclopropyl Ketones and Carbinols2Journal of the American Chemical Society, 1961