(1S, 3R, 4R)-2-Azanorbornyl-3-methanol oxazaborolidines in the asymmetric reduction of ketones
β Scribed by Pedro Pinho; David Guijarro; Pher G. Andersson
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 511 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0040-4020
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Two new optically active l~-amino alcohols 1 and 2 were prepared from Lcystine. The in situ formed chiral oxazaborolidines have been used in the enantioselective catalytic homogeneous borane reduction of prochiral ketones and diketones. The chiral secondary alcohols are obtained with moderate to goo