@article{a0ea636f0b4c48529ae04fd7a137687b,
title = "The photochemistry of cyclononatetraenide and bicyclo4,3,0nonatriene",
abstract = "Cyclononatetraenide ion experiences enhanced basicity on irradiation, and the structures of photo-products of bicyclo4,3,0nonatriene have been determined.",
author = "Jeffrey Schwartz",
note = "Funding Information: In an independent route, excited (111)can close in a disrotatory manner to give (VI). I thank Badische Anilin- und Sodafabrik for a gift of cyclo-octatetraene ; also the Petroleum Research Fund (administered by the American Chemical Society) and the Army Research Office for financial support; and Professors E. E. van Tamelen and J. I. Brauman for advice. (111) (Received, May 28th, 1969; Corn. 738.) t Photolysis and control reaction mixtures were worked up by the addition of these solutions to dry, neat methyl iodide in a nitrogen atmosphere. In experiments where hex-l-yne was converted into butylacetylide, hept-2-yne was produced in this work-up. Copyright: Copyright 2007 Elsevier B.V., All rights reserved.",
year = "1969",
doi = "10.1039/C29690000833",
language = "English (US)",
pages = "833--834",
journal = "Journal of the Chemical Society D: Chemical Communications",
issn = "0577-6171",
publisher = "Royal Society of Chemistry",
number = "14",
}