Concerning methoxy substituent effect and topotactic assistance by methylene chain on photocyclization of n-methylene dicinnamates
- 1 January 1983
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 24 (39) , 4237-4240
- https://doi.org/10.1016/s0040-4039(00)88310-0
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Molecular orbital consideration of the cooperative effect of multiple substituents in some biologically active cinnamate derivatives.CHEMICAL & PHARMACEUTICAL BULLETIN, 1982
- Photocycloaddition in liquid ethyl cinnamate and in ethyl cinnamate glasses. The photoreaction as a probe into the micromorphology of the solidJournal of the American Chemical Society, 1981
- Stereoselective syntheses via a photochemical template effectJournal of the American Chemical Society, 1980
- Marked dependence of multiplicity in direct , photoisomerization of a series of methyl cinnamtes on their -substituentsTetrahedron Letters, 1979
- Photopolymerization in chiral crystals. 3. Toward an "absolute" asymmetric synthesis of optically active dimers and polymers with quantitative enantiomeric yieldJournal of the American Chemical Society, 1979
- Competing reactions of electronically excited 1,3-trimethylene dicinnamateJournal of the American Chemical Society, 1972
- Photosensitized reactions of cinnamate estersThe Journal of Physical Chemistry, 1967
- 383. Topochemistry. Part I. A surveyJournal of the Chemical Society, 1964
- The Photochemical Dimerization of trans-Cinnamic Acid1Journal of the American Chemical Society, 1943
- Geometrical inversion in lightProceedings of the Royal Society of London. Series A, Containing Papers of a Mathematical and Physical Character, 1930