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Total synthesis of the macrolide antibiotic (±)-A26771B

✍ Scribed by Morio Asaoka; Noboru Yanagida; Hisashi Takei

Book ID
107858203
Publisher
Elsevier Science
Year
1980
Tongue
French
Weight
200 KB
Volume
21
Category
Article
ISSN
0040-4039

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📜 SIMILAR VOLUMES

Synthesis of the macrolide antibiotic A2
Synthesis of the macrolide antibiotic A26771B methyl ester
✍ T.A. Hase; E.-L. Nylund 📂 Article 📅 1979 🏛 Elsevier Science 🌐 French ⚖ 210 KB

The total synthesis of the title compound (1) is reported. The isolation and structure elucidation of the 16-membered lactone antibiotic A2677lB (1) from PeniciZZium turbatum (Westling) was recently reportedl. The compound shows optical activity but its absolute (and relative) stereostructure is u

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ChemInform Abstract: Boc2O-Mediated Macrolactonization: Formal Chemoenzymatic Synthesis of Macrolide Antibiotic (-) A26771B.
✍ M. Nagarajan 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

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Stereospecific total synthesis and absol
Stereospecific total synthesis and absolute configuration of a macrocyclic lactone antibiotic, A26771B
✍ Kuniaki Tatsuta; Akira Nakagawa; Shunji Maniwa; Mitsuhiro Kinoshita 📂 Article 📅 1980 🏛 Elsevier Science 🌐 French ⚖ 268 KB

The total synthesis of a sixteen-membered macrocyclic lactone antibiotic, A26771B and its absolute configuration are described by using D-glucose as a chiral source. A 16-membered macrocyclic lactone antibiotic A26771B (&), p reduced by PeraiciZZium turbatwn,