ENANTIOSPECIFIC SYNTHESES OF INTERMEDIATES IN THE TOTAL SYNTHESIS OF PSEUDOMONIC ACIDS
Enantiospecific syntheses of 1S,6S-3,7-dioxabicyclo[4.3.0]non-4-en-8-one (1) and of the enantiomer (2) from D- and L-arabinose respectively have been achieved by two different routes. The conversion of (1) to 6S-(3R-acetanilido)-3,6-dihydro-2H-pyranyl-N,N-dimethylacetamide (3), a key intermediate in...
Main Authors: | Fleet, G, Gough, M |
---|---|
Format: | Journal article |
Language: | English |
Published: |
1982
|
Similar Items
-
ENANTIOSPECIFIC TOTAL SYNTHESIS OF PSEUDOMONIC ACIDS FROM ARABINOSE
by: Fleet, G, et al.
Published: (1983) -
ENANTIOSPECIFIC SYNTHESIS OF (3S-HYDROXY-2S-METHYL) BUTYLTRIPHENYLPHOSPHONIUM IODIDE, A PRECURSOR FOR THE CHIRAL SIDE-CHAIN OF PSEUDOMONIC ACID-C
by: Fleet, G, et al.
Published: (1983) -
MODEL STUDIES ON THE SYNTHESIS OF PSEUDOMONIC ACIDS
by: Fleet, G, et al.
Published: (1982) -
AN APPROACH TO THE ENANTIOSPECIFIC SYNTHESES OF SESBANIMIDE AND ITS ENANTIOMER FROM D-GLUCOSE
by: Fleet, G, et al.
Published: (1984) -
Organocatalytic Enantiospecific Total Synthesis of Butenolides
by: Rudrakshula Madhavachary, et al.
Published: (2021-07-01)