𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Synthesis of Enantiopure Norbornane Derivatives. Effect of Bridgehead Substituent on the π-Facial Selectivity of the Reduction of 2-Norbornanones and Their Oximes.

✍ Scribed by A. GARCIA MARTINEZ; E. TESO VILAR; A. GARCIA FRAILE; S. DE LA MOYA CERERO; P. MARTINEZ RUIZ

Publisher
John Wiley and Sons
Year
2010
Weight
46 KB
Volume
29
Category
Article
ISSN
0931-7597

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: Di-π-methane Photor
ChemInform Abstract: Di-π-methane Photorearrangement of 2,3-Disubstituted Benzobarrelenes and Benzonorbornadienes: Effect of Substituents of Opposite Polarity on the Regioselectivity and Synthesis of Benzopinane Skeleton
✍ Metin Balci 📂 Article 📅 2000 🏛 John Wiley and Sons ⚖ 28 KB

## 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

ChemInform Abstract: A New Halogen-Excha
ChemInform Abstract: A New Halogen-Exchange Reaction Between Sn—F and Li—X: Selective 1,2- and 1,4-Reductions of α,β-Unsaturated Ketones and Effects of Halogen Substituents on the Regioselectivity of Organotin Hydrides.
✍ Takayo Moriuchi-Kawakami; Haruo Matsuda; Ikuya Shibata; Masato Miyatake; Toshihi 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views

A New Halogen-Exchange Reaction Between Sn-F and Li-X: Selective 1,2-and 1,4-Reductions of α,β-Unsaturated Ketones and Effects of Halogen Substituents on the Regioselectivity of Organotin Hydrides. -In dependence of the additive a highly regioselective reduction is obtained under optimized condition

ChemInform Abstract: α,β-Didehydroamino
ChemInform Abstract: α,β-Didehydroamino Acid Derivatives with an Isoxazolyl or a Pyrazolyl Moiety: The Effect of Substituents and Reaction Conditions on Their Stereoselective Formation from 2H-Pyran-2-ones.
✍ Lidija Vranicar; Anton Meden; Slovenko Polanc; Marijan Kocevar 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 42 KB 👁 1 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