103872-61-3Relevant academic research and scientific papers
The Norrish Type II Reaction of Thiophthalimides Having a Benzylic Hydrogen in an N-Alkyl Side Chain
Oda, Kazuaki,Yoshida, Eiichi,Ohno, Kosei,Machida, Minoru,Kanaoka, Yuichi
, p. 642 - 647 (2007/10/02)
Upon irradiation, thiophthalimides (4 and 5) possessing an N-ω-phenylalkyl substituent undergo the Norrish type II cyclization to give tricyclic isoindole derivatives (6-8).In the case of thiophthalimides (11) possessing an indene in the N-side chain, two competitive pathways, the Norrish type II and a Paterno-Buchi like type, were observed.Keywords: thiophthalimide; isoindole; photocyclization; Norrish type II reaction; Paterno-Buchi reaction; thietane; hydrogen abstraction.
THE NORRISH TYPE II REACTION OF THE CYCLIC THIOIMIDES WITH A BENZYLIC HYDROGEN
Machida, Minoru,Oda, Kazuaki,Kanaoka, Yuichi
, p. 5173 - 5174 (2007/10/02)
On irradiation cyclic thioimides with N-ο-phenylalkyl substituents undergo the Norrish type II cyclization when benzylic hydrogen is available at the δ- or ε-position of the thiocarbonyl group.
