Synthesis of the C1′–C11′ portion of pamamycin-607 via a stereoselective oxymercuration of a gamma—silyloxyallene and a stereospecific magnesium—methanol reduction-Reference-Cited by-同舟云学术

Synthesis of the C1′–C11′ portion of pamamycin-607 via a stereoselective oxymercuration of a gamma—silyloxyallene and a stereospecific magnesium—methanol reduction

Published:1988-01 Issue:43 Volume:29 Page:5505-5508
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Walkup Robert D.,Park Gyoosoon

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference9 articles.

1. Pamamycin: A new antibiotic and stimulator of aerial mycelia formation.

2. Structure of pamamycin-607, an aerial mycelium-inducing substance of Streptomyces alboniger

3. Stereoselectivity in the syntheses of substituted 2-(2-tetrahydrofuranyl)acrylates via intramolecular oxymercurations or oxypalladations of allenes

4. Directed reduction of .beta.-hydroxy ketones employing tetramethylammonium triacetoxyborohydride

5. Stereoselective Reduction of ?-Hydroxy-?-ketoesters

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