✦ LIBER ✦

Asymmetric reduction of the carbonyl group by chiral hydrides. 1. Stereochemical considerations

✍ Scribed by V. A. Pavlov; T. V. Simonova; E. I. Klabunovskii

Book ID: 112449415
Publisher: Springer
Year: 1987
Tongue: English
Weight: 447 KB
Volume: 36
Category: Article
ISSN: 1573-9171
DOI: 10.1007/bf00962317

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Asymmetric reductions of carbocations by

Asymmetric reductions of carbocations by chiral organosilicon hydrides. The stereochemical nature of the carbocation captured

✍ Fry, James L.; Adlington, Merwyn G. 📂 Article 📅 1978 🏛 American Chemical Society 🌐 English ⚖ 594 KB

Additions and Corrections - Asymmetric R

Additions and Corrections - Asymmetric Reductions of Carbocations by Chiral Organosilicon Hydrides. The Stereochemical Nature of the Carbocation Captured

✍ Fry, James; Adlington, Merwyn 📂 Article 📅 1979 🏛 American Chemical Society 🌐 English ⚖ 126 KB

Reduction of ?-chlorocarbonyl compounds

Reduction of ?-chlorocarbonyl compounds by the tributyltin hydride?phosphine oxide combined system. Chemoselective reduction of the carbonyl group

✍ Shibata, Ikuya; Suzuki, Taro; Baba, Akio; Matsuda, Haruo 📂 Article 📅 1988 🏛 The Royal Society of Chemistry 🌐 English ⚖ 157 KB

Polymer-assisted asymmetric reactions. I

Polymer-assisted asymmetric reactions. III. The use of crosslinked polymers containing chiral amino-alcohol or polyol pendant groups in asymmetric hydride reductions

✍ Pierre Lecavalier; Edward Bald; Ying Jiang; Jean M.J. Fréchet; Philip Hodge 📂 Article 📅 1985 🏛 Elsevier Science ⚖ 845 KB

ChemInform Abstract: Stereochemically Co

ChemInform Abstract: Stereochemically Controlled Asymmetric 1,2-Reduction of Enones Mediated by a Chiral Sulfoxide Moiety and a Lanthanum(III) Ion.

✍ Shigeyasu Motohashi; Kouichi Nagase; Toshinori Nakakita; Takeshi Matsuo; Yoshika 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 43 KB

## Abstract Reduction of (Z)‐β‐sulfinyl enones with NaBH~4~/ LaCl~3~·7H~2~O allows efficient access to enantiomerically pure allylic alcohols after desulfuration.

Asymmetric reduction of ethyl benzoylfor

Asymmetric reduction of ethyl benzoylformate with chiral NADH model systems: Mechanistic and stereochemical consideration of the reactions based on the complexation properties of the model compounds

✍ Masaki Amano; Naomichi Baba; Jun'ichi Oda; Yuzo Inouye 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 800 KB