The total synthesis of (+)-ryanodol. Part III. Preparation of (+)-anhydroryanodol from a key pentacyclic intermediate

DOI: 10.1139/v90-023

Source and publish data:

Canadian Journal of Chemistry p. 153 - 185 (1990)

Update date:2022-08-05

Topics: Oxidation   Regioselectivity   Crystallization   Yield   NMR spectroscopy   Mass spectrometry   Stereochemistry   Reduction   Chromatography   Total synthesis   Enantioselective synthesis   Deprotection   TLC (thin-layer chromatography)   HPLC (high-performance liquid chromatography)   Protecting group   Retrosynthetic analysis   Reaction Optimization  

Authors:

Deslongchamps

Belanger

Berney

Borschberg

Brousseau r.

Doutheau

Durand

Katayama

Lapalme

Leturc

Liao

MacLachlan

Maffrand

Marazza

Martino

Moreau

Ruest

Saint-Laurent

Saintonge