𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Highly Efficient and Stereoselective Radical Addition of Tertiary Amines to Electron-Deficient Alkenes — Application to the Enantioselective Synthesis of Necine Bases.

✍ Scribed by Samuel Bertrand; Norbert Hoffmann; Jean-Pierre Pete

Publisher
John Wiley and Sons
Year
2001
Weight
42 KB
Volume
32
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: Stereoselective Rad
ChemInform Abstract: Stereoselective Radical Addition of Tertiary Amines to (5R)-5-Menthyloxy-2[5H]-furanone: Application to the Enantioselective Synthesis of (-)-Isoretronecanol and (+)-Laburnine.
✍ Samuel Bertrand; Norbert Hoffmann; Jean-Pierre Pete 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

Application to the Enantioselective Synthesis of (-)-Isoretronecanol and (+)-Laburnine. -Compound (I) is an adduct of a stereoselective radical addition of a tertiary amine with (5R)-5-menthyloxy-2[5H]-furanone. It is readily transformed to (+)-laburnine (IV) in a three-step sequence. Similarly, (-