✦ LIBER ✦

ChemInform Abstract: Asymmetric Synthesis of (S)-Arylalkanols by Microbial Reduction.

✍ Scribed by K. NAKAMURA; T. MATSUDA; A. OHNO

Publisher: John Wiley and Sons
Year: 2010
Weight: 29 KB
Volume: 28
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199707046

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Asymmetric Reductio

ChemInform Abstract: Asymmetric Reduction of Imines

✍ S. HASHIGUCHI; N. UEMATSU; R. NOYORI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 24 KB 👁 1 views

ChemInform Abstract: Microbial Asymmetri

ChemInform Abstract: Microbial Asymmetric Reduction of α-Hydroxyketones in the anti-Prelog Selectivity.

✍ Toshikuni Tsujigami; Takeshi Sugai; Hiromichi Ohta 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB

ChemInform Abstract: An Efficient Synthe

ChemInform Abstract: An Efficient Synthesis of a Key Intermediate of DU-6859a via Asymmetric Microbial Reduction.

✍ K. SATOH; A. IMURA; A. MIYADERA; K. KANAI; Y. YUKIMOTO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views

ChemInform Abstract: Diastereo- and Enan

ChemInform Abstract: Diastereo- and Enantioselective Synthesis of Dimethylcyclohexanamines by Asymmetric Reductive Amination.

✍ B. SPECKENBACH; P. BISEL; A. W. FRAHM 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

ChemInform Abstract: Asymmetric Synthesi

ChemInform Abstract: Asymmetric Synthesis of Corsifuran A by an Enantioselective Oxazaborolidine Reduction.

✍ Harry Adams; Nathan J. Gilmore; Simon Jones; Mark P. Muldowney; Stephan H. von R 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 16 KB 👁 2 views

## 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 “Full Text” option. The original article is trackable v

ChemInform Abstract: Stereoselective Syn

ChemInform Abstract: Stereoselective Synthesis of Sphinganine by Means of Modified Asymmetric Borane Reduction.

✍ M. MASUI; T. SHIOIRI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB

Stereoselective Synthesis of Sphinganine by Means of Modified Asymmetric Borane Reduction. -A modified asymmetric borane reduction of the ester (I) and the related silyl ether (V) are described. Thus, reduction of the ester yields mainly the threo compound, whereas the silyl ether affords the desir