A synthesis of l-cyano-5-methoxy-2-tetralone (I) from 5-methoxy-2-tetralone via the hydroxymethylene derivative and the corresponding isoxazole, m.p. 137' , vma,(Nujol) 1658, 1605, 1580 cm.-', A,,(EtOH) 274 q\_t(1,740), 280 ~(1,950), has recently been reported by Pellet&x and Parthasarathy (1).
Microbial reduction of 2-cyano-1-tetralones
✍ Scribed by Maryam Mehmandoust; Didier Buisson; Robert Azerad
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 156 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The microbial reduction of ~-ketoesters derived from 2-tetralone has been shown to produce good yields of 2-hydroxy-l-carboxy-or 3-hydroxy-2-carboxyesters. Baker's yeast invariably affords a high enantiomeric purity cis-hydroxyester, while fungi strains may produce, sometimes exclusively, cisor tran
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v