Photochemistry of Arylidene-β-ionones: A Highly Efficient Route to Novel Tricyclic Ketones through Intramolecular, Exoselective Photochemical (4 + 2) Cycloadditions, Occurring Only in an Aqueous−Organic Solvent-Reference-Cited by-同舟云学术

Photochemistry of Arylidene-β-ionones: A Highly Efficient Route to Novel Tricyclic Ketones through Intramolecular, Exoselective Photochemical (4 + 2) Cycloadditions, Occurring Only in an Aqueous−Organic Solvent

Published:2002-03-08 Issue:7 Volume:67 Page:2234-2240
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ishar Mohan Paul S.¹,Singh Rajinder¹,Kumar Kamal¹,Singh Gurmit¹,Velmurugan D.¹,Pandi A. Subbiah¹,Raj S. S. Sundra¹,Fun H. K.¹

Affiliation:

1. Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar 143005, Punjab, India, Department of Crystallography and Biophysics, University of Madras, Guindy campus, Chennai 600 025, Tamilnadu, India, and X -ray Division, Department of Physics, Universiti Sains Malaysia, Pinang, Malaysia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo010963w

Reference39 articles.

1. Regioselective Photoelectrocyclization of (E/E)-Arylidene-β-ionones; Synthesis of Some 1,7,7-trimethyl-3-(e-2′-arylethenyl)-2-oxabicyclo [4.4.0] Deca-3,5-dienes

2. Photochemical reorganisation of 1,7,7-trimethyl-3-(E-2′-arylethenyl)-2-oxabicyclo[4.4.0]deca-3,5-dienes

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