Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5280075 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
The enantiodifferentiating [4+4] photocyclodimerization of anthracenecarboxylic acid (AC) mediated by native, mono- and di-3,6-anhydro-γ-cyclodextrins was investigated in both aqueous solution and solid-state. The solid-state photolyses gave inherently disfavored head-to-head photodimers in much higher chemical and optical yields than in the aqueous solution.
Related Topics
Physical Sciences and Engineering
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Authors
Cheng Yang, Masaki Nishijima, Asao Nakamura, Tadashi Mori, Takehiko Wada, Yoshihisa Inoue,