𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Practical, One-Step Synthesis of Optically Active β-Lactones via the Tandem Mukaiyama Aldol—Lactonization (TMAL) Reaction.

✍ Scribed by H. W. YANG; D. ROMO

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

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Diastereoselective
ChemInform Abstract: Diastereoselective Synthesis of Tetrahydrofurans via Mead Reductive Cyclization of Keto-β-Lactones Derived from the Tandem Mukaiyama Aldol Lactonization (TMAL) Process.
✍ T. Andrew Mitchell; Daniel Romo 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 59 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 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: Synthesis of β-Lact
ChemInform Abstract: Synthesis of β-Lactones. Part 9. Synthesis of Enantiomerically Pure β-Lactones by the Tandem Aldol—Lactonization. A Highly Efficient Access to (3S,4S)-3-Hexyl-4-[(2S)-2-hydroxytridecyl]oxetan-2-one (IV), the Key Intermediate for the Enzyme Inhibitors Tetrahydrolipstatin (VIa) and Tetrahydroesterastin (VIb).
✍ Christine Wedler; Burckhard Costisella; Hans Schick 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views