Effect of a Strategically Positioned Methoxy Substituent on the Photochemistry of 3-Aryl-3H-1-Oxacyclopenta[l]Phenanthren-2-Ones
Joint Authors
Prathapan, Sreedharan
Rath, Nigam P.
Unnikrishnan, Perupparampil A.
Thumpakara, Roshini K.
Jose, Binoy
Source
Organic Chemistry International
Issue
Vol. 2010, Issue 2010 (31 Dec. 2010), pp.1-5, 5 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2010-12-28
Country of Publication
Egypt
No. of Pages
5
Main Subjects
Abstract EN
Irradiation of 3-methoxy-3-aryl-3H-1-oxacyclopenta[l]phenanthren-2-one derivatives 5a–d resulted in singlet-mediated decarbonylation reaction leading to the formation of phenanthrene derivatives 9a–d.
The structure of the photoproduct was unequivocally established on the basis of X-ray crystallographic analysis.
American Psychological Association (APA)
Thumpakara, Roshini K.& Jose, Binoy& Unnikrishnan, Perupparampil A.& Prathapan, Sreedharan& Rath, Nigam P.. 2010. Effect of a Strategically Positioned Methoxy Substituent on the Photochemistry of 3-Aryl-3H-1-Oxacyclopenta[l]Phenanthren-2-Ones. Organic Chemistry International،Vol. 2010, no. 2010, pp.1-5.
https://search.emarefa.net/detail/BIM-496956
Modern Language Association (MLA)
Thumpakara, Roshini K.…[et al.]. Effect of a Strategically Positioned Methoxy Substituent on the Photochemistry of 3-Aryl-3H-1-Oxacyclopenta[l]Phenanthren-2-Ones. Organic Chemistry International No. 2010 (2010), pp.1-5.
https://search.emarefa.net/detail/BIM-496956
American Medical Association (AMA)
Thumpakara, Roshini K.& Jose, Binoy& Unnikrishnan, Perupparampil A.& Prathapan, Sreedharan& Rath, Nigam P.. Effect of a Strategically Positioned Methoxy Substituent on the Photochemistry of 3-Aryl-3H-1-Oxacyclopenta[l]Phenanthren-2-Ones. Organic Chemistry International. 2010. Vol. 2010, no. 2010, pp.1-5.
https://search.emarefa.net/detail/BIM-496956
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-496956
