Formal total synthesis of (−)-salicylihalamides A and B is described starting with a nonracemic chiral epoxide obtained from Jacobsen's kinetic resolution. Sharpless asymmetric epoxidation, Diels Alder reaction, Mitsunobu coupling and ring closing metathesis are the other key steps involved
Two different approaches to the enantioselective syntheses of (+)-sedamine and (−)-allosedamine are ...
Titanium tetrachloride promoted reaction of silyl ketene acetals with epoxides, followed by acidic w...
Abstract The first part of this monograph discusses the asymmetric, ylide based, reagent controlle...
Formal total synthesis of (−)-salicylihalamides A and B is described starting with a nonracemic chir...
Stereoselective synthesis of the macrocyclic core of salicylihalamides A and B is described. The syn...
A concise total synthesis of the potent cytotoxic marine natural products salicylihalamide A and B (...
An efficient synthesis of the macrolactone 3 of the salicylihalamides in 10 linear steps from alkene...
A stereoselective and convergent formal approach to Salicylihalamide A and B is achieved through our...
The first part of this dissertation describes the total synthesis of (+)- and (−)-salicylihalamide A...
This thesis describes studies toward the synthesis of enamide macrolide salicylihalamide A (1). The...
Enantiomerically pure terminal 1,2-diols are important synthetic intermediates.1 A number of synthet...
The sodium salt of (S)-sulfimide 8 reacts with carbonyl compounds to yield (R)-epoxides in 60-64% yi...
A highly stereoselective formal total synthesis of the ornithine decarboxylase inhibitors (-)-salini...
This report presents the applications of enantioselective epoxidation of prochiral allylic alcohols,...
Asymmetric total synthesis of (+)-epilupinine was achieved in just three steps using only commercial...
Two different approaches to the enantioselective syntheses of (+)-sedamine and (−)-allosedamine are ...
Titanium tetrachloride promoted reaction of silyl ketene acetals with epoxides, followed by acidic w...
Abstract The first part of this monograph discusses the asymmetric, ylide based, reagent controlle...
Formal total synthesis of (−)-salicylihalamides A and B is described starting with a nonracemic chir...
Stereoselective synthesis of the macrocyclic core of salicylihalamides A and B is described. The syn...
A concise total synthesis of the potent cytotoxic marine natural products salicylihalamide A and B (...
An efficient synthesis of the macrolactone 3 of the salicylihalamides in 10 linear steps from alkene...
A stereoselective and convergent formal approach to Salicylihalamide A and B is achieved through our...
The first part of this dissertation describes the total synthesis of (+)- and (−)-salicylihalamide A...
This thesis describes studies toward the synthesis of enamide macrolide salicylihalamide A (1). The...
Enantiomerically pure terminal 1,2-diols are important synthetic intermediates.1 A number of synthet...
The sodium salt of (S)-sulfimide 8 reacts with carbonyl compounds to yield (R)-epoxides in 60-64% yi...
A highly stereoselective formal total synthesis of the ornithine decarboxylase inhibitors (-)-salini...
This report presents the applications of enantioselective epoxidation of prochiral allylic alcohols,...
Asymmetric total synthesis of (+)-epilupinine was achieved in just three steps using only commercial...
Two different approaches to the enantioselective syntheses of (+)-sedamine and (−)-allosedamine are ...
Titanium tetrachloride promoted reaction of silyl ketene acetals with epoxides, followed by acidic w...
Abstract The first part of this monograph discusses the asymmetric, ylide based, reagent controlle...
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