TY - JOUR
T1 - The photochemistry of cyclononatetraenide and bicyclo4,3,0nonatriene
AU - Schwartz, Jeffrey
N1 - 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.
PY - 1969
Y1 - 1969
N2 - Cyclononatetraenide ion experiences enhanced basicity on irradiation, and the structures of photo-products of bicyclo4,3,0nonatriene have been determined.
AB - Cyclononatetraenide ion experiences enhanced basicity on irradiation, and the structures of photo-products of bicyclo4,3,0nonatriene have been determined.
UR - https://www.scopus.com/pages/publications/37049118929
UR - https://www.scopus.com/pages/publications/37049118929#tab=citedBy
U2 - 10.1039/C29690000833
DO - 10.1039/C29690000833
M3 - Article
AN - SCOPUS:37049118929
SN - 0577-6171
SP - 833
EP - 834
JO - Journal of the Chemical Society D: Chemical Communications
JF - Journal of the Chemical Society D: Chemical Communications
IS - 14
ER -