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Synthesis of Enantiomerically Pure β-Lactones by the Tandem Aldol−Lactonization. A Highly Efficient Access to (3 S ,4 S )-3-Hexyl-4- [(2 S )-2-hydroxytridecyl]oxetan-2-one, the Key Intermediate for the Enzyme Inhibitors Tetrahydrolipstatin and Tetrahydroesterastin †,1

✍ Scribed by Wedler, Christine; Costisella, Burckhard; Schick, Hans

Book ID
120175989
Publisher
American Chemical Society
Year
1999
Tongue
English
Weight
50 KB
Volume
64
Category
Article
ISSN
0022-3263

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📜 SIMILAR VOLUMES

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