A concise asymmetric synthetic route to two new tetrahydroxyindolizidinone and quinolizidinone derivatives has been developed from a common intermediate which featured a highly selective dihydroxylation reaction and a RCM reaction as key steps
L-Glutamic diethyl ester hydrochloride was converted to its pyrrole derivative 22 by condensation wi...
Convenient accesses to enantiomerically pure 2-, 2,3-, 2,6-, 2,3,6-substituted piperidines and 1,4-s...
A direct approach to the synthesis of indolizidine and quinolizidine scaffolds of iminosugars is des...
This account describes an overview of the asymmetric syntheses of pyrrolizidines, indolizidines and ...
We have developed a highly efficient cascade sequence for asymmetric synthesis of indoloquinolizidin...
Concise asymmetric syntheses of (-)-lupinine, (+)-isoretronecanol, (+)-5-epi-tashiromine and (R,R)-1...
BackgroundIndolizidine alkaloids widely occur in nature and display interesting biological activity....
Asymmetric synthesis of indoloquinolizidine has been accomplished by using acyl pyridinium salt bear...
Abstract: The use of Vinylogous urethanes as pivotal intermediates m the synthesis of mdolizidine al...
In this study, two possible regiochemical pathways of aziridine ring opening, termed "regiochem...
International audienceUsing d-glyceraldehyde acetonide as a starting material, a four-step synthesis...
Background: Prior work from these laboratories has centred on the development of enaminones as versa...
Indolo[2,3-a]quinolizines have been prepared in enantiomerically pure form by a very short and effic...
A direct method for the synthesis of new azasugars-like compounds has been developed, which involves...
The asymmetric syntheses of pyrrolizidine, indolizidine and quinolizidine alkaloids have been achiev...
L-Glutamic diethyl ester hydrochloride was converted to its pyrrole derivative 22 by condensation wi...
Convenient accesses to enantiomerically pure 2-, 2,3-, 2,6-, 2,3,6-substituted piperidines and 1,4-s...
A direct approach to the synthesis of indolizidine and quinolizidine scaffolds of iminosugars is des...
This account describes an overview of the asymmetric syntheses of pyrrolizidines, indolizidines and ...
We have developed a highly efficient cascade sequence for asymmetric synthesis of indoloquinolizidin...
Concise asymmetric syntheses of (-)-lupinine, (+)-isoretronecanol, (+)-5-epi-tashiromine and (R,R)-1...
BackgroundIndolizidine alkaloids widely occur in nature and display interesting biological activity....
Asymmetric synthesis of indoloquinolizidine has been accomplished by using acyl pyridinium salt bear...
Abstract: The use of Vinylogous urethanes as pivotal intermediates m the synthesis of mdolizidine al...
In this study, two possible regiochemical pathways of aziridine ring opening, termed "regiochem...
International audienceUsing d-glyceraldehyde acetonide as a starting material, a four-step synthesis...
Background: Prior work from these laboratories has centred on the development of enaminones as versa...
Indolo[2,3-a]quinolizines have been prepared in enantiomerically pure form by a very short and effic...
A direct method for the synthesis of new azasugars-like compounds has been developed, which involves...
The asymmetric syntheses of pyrrolizidine, indolizidine and quinolizidine alkaloids have been achiev...
L-Glutamic diethyl ester hydrochloride was converted to its pyrrole derivative 22 by condensation wi...
Convenient accesses to enantiomerically pure 2-, 2,3-, 2,6-, 2,3,6-substituted piperidines and 1,4-s...
A direct approach to the synthesis of indolizidine and quinolizidine scaffolds of iminosugars is des...