The mechanism of the photoconversion of .alpha.-phenylcinnamic esters into 9,10-dihydrophenanthrenes-Reference-Cited by-同舟云学术

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The mechanism of the photoconversion of .alpha.-phenylcinnamic esters into 9,10-dihydrophenanthrenes

Published:1977-10 Issue:22 Volume:99 Page:7221-7224
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Op het Veld P. H. G.,Laarhoven W. H.

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja00464a021

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2. Photochemical cyclizations and intramolecular cycloadditions of conjugated arylolefins: Part 2: Photocyclizations without dehydrogenation and photocycloadditions;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02

3. Medium-size Cyclophanes, 71. Synthesis, Structures and Photo-Induced Cyclisation of 1,2-Diphenyl[2.n]Metacyclophan-1-Enes;Journal of Chemical Research;2006-09

4. 4n+2 Systems: Molecules Derived from Z-Hexa-1,3,5-Triene/Cyclohexa-1,3-Diene;Photochromism;2003

5. Sandmeyer reactions. Part 4.1 An investigation into the cyclisation modes of Pschorr phenanthrene synthesis;Journal of the Chemical Society, Perkin Transactions 2;1999

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