✦ LIBER ✦

Asymmetric Induction by β-Cyclodextrins in NaBH4 Reduction of Ketones

✍ Scribed by Kwanghee Koh Park; Woo-Jeon Sim; Joon Woo Park

Book ID: 110256467
Publisher: Springer Netherlands
Year: 1997
Tongue: English
Weight: 73 KB
Volume: 27
Category: Article
ISSN: 0923-0750
DOI: 10.1023/a:1007937115071

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

γ-Cyclodextrin-Bicapped C60-Mediated Asy

γ-Cyclodextrin-Bicapped C60-Mediated Asymmetric Reduction of Ketones with NaBH4.

✍ Takahiro Nishimura; Mitsuru Nakajima; Yasunari Maeda; Sakae Uemura; Shin-ichi Ta 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 20 KB 👁 1 views

Epimerization in the NaBH4 reduction of

Epimerization in the NaBH4 reduction of asymmetric ketones

✍ V. Hach; Elizabeth C. Fryberg; Elizabeth McDonald 📂 Article 📅 1971 🏛 Elsevier Science 🌐 French ⚖ 235 KB

ChemInform Abstract: Chirally Modified N

ChemInform Abstract: Chirally Modified NaBH4/ZrCl4 Promoted Asymmetric Reduction of Prochiral Ketones.

✍ K. Purushothama Chary; R. Mathew Thomas; D. S. Iyengar 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 2 views

## 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

Synthesis of Optically Active α,β-Unsatu

Synthesis of Optically Active α,β-Unsaturated Triazolyl Alcohols via Asymmetric NaBH4 Reduction of the Corresponding Ketones.

✍ Zhenghong Zhou; Yilong Tang; Lixin Wang; Guofeng Zhao; Qilin Zhou; Chuchi Tang 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 36 KB

## Abstract For Abstract see ChemInform Abstract in Full Text.

Synthesis of Optically Active α,β‐Unsatu

Synthesis of Optically Active α,β‐Unsaturated Triazolyl Alcohols via Asymmetric NaBH 4 Reduction of the Corresponding Ketones

✍ Zhou, Zhenghong; Tang, Yilong; Wang, Lixin; Zhao, Guofeng; Zhou, Qilin; Tang, Ch 📂 Article 📅 2004 🏛 Taylor and Francis Group 🌐 English ⚖ 140 KB

Reductions of α,β-Unsaturated Ketones by

Reductions of α,β-Unsaturated Ketones by NaBH4 or NaBH4 + CoCl2: Selectivity Control by Water or by Aqueous Micellar Solutions

✍ Andrea Aramini; Lucia Brinchi; Raimondo Germani; Gianfranco Savelli 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 209 KB 👁 1 views

Operationally simple and environmentally benign procedures have been developed to selectively reduce different α,βunsaturated ketones, 4,4-dimethylcyclohex-2-ene-1-one (1), isophorone (2), benzylideneacetone (3), chalcone (4) by NaBH 4 or by the system NaBH 4 + CoCl 2 . Alternative reaction media to