✦ LIBER ✦

ChemInform Abstract: Asymmetric Synthesis of (-)-Indolizidines 167B (IXa) and 209D (IXb) Based on Stereocontrolled Allylation of a Chiral Tricyclic N-Acyl-N,O-acetal.

✍ Scribed by Naoki Yamazaki; Toshimasa Ito; Chihiro Kibayashi

Publisher: John Wiley and Sons
Year: 2010
Weight: 31 KB
Volume: 31
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200021216

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Stereoselective Syn

ChemInform Abstract: Stereoselective Synthesis of (.+-.)-Indolizidines 167B and 209D and Their trans-Isomers Based on the Reductive Allylboration of Pyridine.

✍ YU. N. BUBNOV; E. V. KLIMKINA; A. V. IGNATENKO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 38 KB

Stereoselective Synthesis of (±)-Indolizidines 167B and 209D and Their trans-Isomers Based on the Reductive Allylboration of Pyridine. -A new and general method for the stereoselective synthesis of 5-substituted indolizidines based on the intramolecular cyclization of 2allyltetrahydropyridines, rea

ChemInform Abstract: Stereoselective Syn

ChemInform Abstract: Stereoselective Synthesis of a Chiral Synthon, 2,2,5-Trisubstituted Tetrahydropyran, Based on Simultaneous 1,3- and 1,6-Asymmetric Induction via Nucleophilic Acetal Cleavage Reaction of the Bicyclic Acetal: A Total Synthesis of (-)-Malyngolide.

✍ N. MAEZAKI; Y. MATSUMORI; T. SHOGAKI; M. SOEJIMA; T. TANAKA; H. OHISHI; IWATA C. 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB 👁 2 views