Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1323842 | Journal of Organometallic Chemistry | 2006 | 8 Pages |
Abstract
The photolysis of cis- and trans-1,2-dimethyl-1,2-diphenyl-1,2-disilacyclohexane (1a and 1b) with tert-butyl alcohol proceeded with high stereospecificity to give cis- and trans-addition/elimination product (2a and 2b), while with acetone, 1a and 1b afforded cis- and trans-ene-adduct, respectively.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Akinobu Naka, Kuninori Nakano, Mitsuo Ishikawa, Young-Woo Kwak,