✦ LIBER ✦

ChemInform Abstract: Organosilicon Chemistry. Part. 150. Tandem Aldol—Reduction Reaction of Dimethylsilyl Enolates: A New Method for Stereoselective Preparation of 1,3-Diols.

✍ Scribed by Katsukiyo Miura; Takahiro Nakagawa; Shuntaro Suda; Akira Hosomi

Publisher: John Wiley and Sons
Year: 2010
Weight: 30 KB
Volume: 31
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200024097

No coin nor oath required. For personal study only.

✦ Synopsis

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 via the “References” option.

📜 SIMILAR VOLUMES

ChemInform Abstract: Tandem Aldol—Tishch

ChemInform Abstract: Tandem Aldol—Tishchenko Reactions of Lithium Enolates: A Highly Stereoselective Method for Diol and Triol Synthesis.

✍ P. M. BODNAR; J. T. SHAW; K. A. WOERPEL 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

ChemInform Abstract: Stereoselective Red

ChemInform Abstract: Stereoselective Reductive Rearrangement of α-Hydroxy Epoxides: A New Method for Synthesis of 1,3-Diols.

✍ Yong Qiang Tu; Liang Dong Sun; Ping Zhen Wang 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB