𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stereoselective cyclopropanation and ring-opening: Application to the synthesis of pure (S)-2-methyl-3-arylpropylamines

✍ Scribed by Marin Roje; Vladimir Vinković; Vitomir Šunjić; Arlette Solladié-Cavallo; Anh Diep-Vohuule; Thomas Isarno


Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
410 KB
Volume
54
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


ChemInform Abstract: Stereoselective Cyc
✍ M. ROJE; V. VINKOVIC; V. SUNJIC; A. SOLLADIE-CAVALLO; A. DIEP-VOHUULE; T. ISARNO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 2 views

Stereoselective Cyclopropanation and Ring-Opening: Application to the Synthesis of Pure (S)-2-Methyl-3-arylpropylamines. -A short synthesis (6 steps) of the (S)-enantiomers (I) and (II) of the fungicides fenpropimorph and fenpropidine is presented. The required trans-isomers (VI) of the cyclopropan

A Highly Stereoselective Synthesis of th
✍ Steven M. Allin; Christopher I. Thomas; James E. Allard; Kevin Doyle; Mark R. J. 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 162 KB

## Abstract We present a facile and highly stereoselective approach to the indolo[2,3‐__a__]quinolizine ring system from a readily available, non‐racemic chiral template. We demonstrate the potential for application of this methodology to natural product synthesis through conversion of the template

ChemInform Abstract: Ring-Opening Hydrof
✍ Alexander J. Cresswell; Stephen G. Davies; James A. Lee; Melloney J. Morris; Pau 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 33 KB

## Abstract The reaction allows a simple, efficient, and highly stereoselective (< 98% d.e.) access to synthetically and biologically important fluorohydrins.