Abstract
Four methods of asymmetric induction in the cis,trans-photoisomerization of 2β,3β-diphenylcyclopropane-1α-carboxylic acid derivatives were studied. Best results (ca. 80% de) were obtained by irradiation of chiral esters, amides, and salts in NaY and LiY zeolites and in the pure crystalline state.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 2801-2804 |
| Number of pages | 4 |
| Journal | Organic letters |
| Volume | 2 |
| Issue number | 18 |
| State | Published - Sep 7 2000 |
| Externally published | Yes |
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
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Cheung, E., Chong, K. C. W., Jayaraman, S., Ramamurthy, V., Scheffer, J. R., & Trotter, J. (2000). Enantio- and diastereodifferentiating cis,trans-photoisomerization of 2β,3β-diphenylcyclopropane-1α-carboxylic acid derivatives in organized media. Organic letters, 2(18), 2801-2804.