fulltext.study @t Gmail

Formation of cyclooctatriene and bicyclooctadiene through regioselective intermolecular (2 + 2) photocycloaddition of benzoic acids to allyl alcohol in water

Paper ID Volume ID Publish Year Pages File Format Full-Text
28283 44067 2009 5 PDF Available
Title
Formation of cyclooctatriene and bicyclooctadiene through regioselective intermolecular (2 + 2) photocycloaddition of benzoic acids to allyl alcohol in water
Abstract

The regioselective intermolecular (2 + 2) photocycloaddition of the sodium salt of benzoic acids 1 to allyl alcohol 2 proceeded in water to afford cyclooctatrienes 3 and bicyclooctadienes 4. The efficiency and product distribution of this photoreaction were strongly influenced by the substituent of benzoic acid and solvent polarity. The photocycloaddition of benzoic acids in water is an environmentally friendly method for the preparation of cyclooctatriene and bicyclooctadiene.

Keywords
Cyclooctatriene; Bicyclooctadiene; Regioselective intermolecular (2 + 2) photocycloaddition; Water; Benzoic acid; Allyl alcohol
First Page Preview
Formation of cyclooctatriene and bicyclooctadiene through regioselective intermolecular (2 + 2) photocycloaddition of benzoic acids to allyl alcohol in water
Get Full-Text Now
Don't Miss Today's Special Offer
Price was $35.95
You save - $31
Price after discount Only $4.95
100% Money Back Guarantee
Full-text PDF Download
Online Support
Any Questions? feel free to contact us
Publisher
Database: Elsevier - ScienceDirect
Journal: Journal of Photochemistry and Photobiology A: Chemistry - Volume 202, Issues 2–3, 25 February 2009, Pages 235–239
Authors
, , , , , ,
Subjects
Physical Sciences and Engineering Chemical Engineering Bioengineering
Get Full-Text Now
Don't Miss Today's Special Offer
Price was $35.95
You save - $31
Price after discount Only $4.95
100% Money Back Guarantee
Full-text PDF Download
Online Support
Any Questions? feel free to contact us