✦ LIBER ✦

Asymmetric Synthesis of the Polyol Subunit (I) of the Macrolide Antibiotic, Ossamycin (II).

✍ Scribed by Noriki Kutsumura; Shigeru Nishiyama

Publisher: John Wiley and Sons
Year: 2005
Weight: 15 KB
Volume: 36
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200550197

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Asymmetric Synthesis of the Polyol Subun

Asymmetric Synthesis of the Polyol Subunit of the Macrolide Antibiotic, Ossamycin: A Unique Approach Utilizing Stereochemical Specificity.

✍ Noriki Kutsumura; Shigeru Nishiyama 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 27 KB

Asymmetric Synthesis of the Polyol Subun

Asymmetric Synthesis of the Polyol Subunit of the Polyene Macrolide Antibiotic RK-397.

✍ Sandrine Gerber-Lemaire; Ana T. Carmona; Kai T. Meilert; Pierre Vogel 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 11 KB

Synthesis of the Antifungal Macrolide An

Synthesis of the Antifungal Macrolide Antibiotic (+)-Roxaticin (I).

✍ David A. Evans; Brian T. Connell 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 59 KB 👁 1 views

Synthesis of the Macrolide Core (I) of M

Synthesis of the Macrolide Core (I) of Migrastatin (II).

✍ Christoph Gaul; Samuel J. Danishefsky 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 68 KB 👁 2 views

A Concise Asymmetric Route to the Antibi

A Concise Asymmetric Route to the Antibiotic Macrolides Patulolide A (I) and Pyrenophorin (II).

✍ K. Srinivasa Rao; D. Srinivasa Reddy; K. Mukkanti; Manojit Pal; Javed Iqbal 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 14 KB

ChemInform Abstract: Synthesis of Amphot

ChemInform Abstract: Synthesis of Amphotericin B, a Convergent Strategy to the Polyol Segment of the Heptaene Macrolide Antibiotics.

✍ G. J. MCGARVEY; J. A. MATHYS; K. J. WILSON 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Synthesis of Amphotericin B, a Convergent Strategy to the Polyol Segment of the Heptaene Macrolide Antibiotics. -The key step in the synthesis of the ester (VIII), a potent precursor of amphotericin B, is stereoselective cycloaddition of the dipolarophile (III) to the nitrile oxide generated from t