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
✦ 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
ChemInform Abstract: Stereoselective Syn
✍
Philippe Dorizon; Guifa Su; Gitte Ludvig; Lilyia Nikitina; Renee Paugam; Jean Ol
📂
Article
📅
2010
🏛
John Wiley and Sons
⚖ 34 KB
👁 2 views
Reductive Ring-Opening of Phthalan and I
✍
Daniel García; Francisco Foubelo; Miguel Yus
📂
Article
📅
2010
🏛
John Wiley and Sons
🌐
English
⚖ 551 KB
ChemInform Abstract: Reductive Ring-Open
✍
Daniel Garcia; Francisco Foubelo; Miguel Yus
📂
Article
📅
2010
🏛
John Wiley and Sons
⚖ 50 KB
👁 1 views
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.