✦ LIBER ✦

Stereospecific synthesis of (+)-oxybiotin from D-xylose. Preparation of the final chiral (+)-oxybiotin precursor

✍ Scribed by Dusˇan Miljkovic´; Velimir Popsavin; Ja´nos Harangi

Publisher: Elsevier Science
Year: 1987
Tongue: French
Weight: 183 KB
Volume: 28
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)96827-8

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The stereospecific synthesis of an 11-ox

The stereospecific synthesis of an 11-oxaprostaglandin analog from D-xylose

✍ Gerhardus J. Lourens; J.M. Koekemoer 📂 Article 📅 1975 🏛 Elsevier Science 🌐 French ⚖ 193 KB

ChemInform Abstract: Stereospecific Synt

ChemInform Abstract: Stereospecific Synthesis of (-)-allo-Muscarine from D-Glucose: Novel Routes to the Key Chiral Synthon.

✍ V. POPSAVIN; O. BERIC; M. POPSAVIN; J. CSANADI; S. LAJSIC; D. MILJKOVIC 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

Stereospecific Synthesis of (-)-allo-Muscarine from D-Glucose: Novel Routes to the Key Chiral Synthon. -A simple and convenient four-step conversion of L-idose (I), which is readily available from D-glucose, to key intermediate (VI) in the (-)-allo-muscarine (VII) synthesis is described. Compared t

Enantiopure Hydroxylactones from D-Xylos

Enantiopure Hydroxylactones from D-Xylose. A Novel Approach to the Enantiodivergent Synthesis of (+)- and (-)-Muricatacin Suitable for the Preparation of 7-Oxa Analogues.

✍ Velimir Popsavin; Ivana Krstic; Mirjana Popsavin 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 111 KB

Chiral α-hydroxy- and α,β-dihydroxy- ald

Chiral α-hydroxy- and α,β-dihydroxy- aldehydes from D-isoascorbic and L-ascorbic acids. Useful precursors for the synthesis of fatty acid metabolites.

✍ Y Le Merrer; C Gravier-Pelletier; J Dumas; J.C Depezay 📂 Article 📅 1990 🏛 Elsevier Science 🌐 French ⚖ 273 KB

&mm6fy : The four possible stereoisomers of a$dihydroxyaldehydes, useful building blocks for the synthesis of fatty acids metabolites, are synthesized via epoxy-tetrols derived from D-isoascorbic and L-ascorbic acids. The general method we develop allows the synthesis of chiral a-hydroxyaldehydes as