International audienceUsing d-glyceraldehyde acetonide as a starting material, a four-step synthesis of enantiomerically pure 3,4-dihydroxyquinolizidines is described. The key steps of the synthesis consist of a Mitsunobu ring-closing reaction and the subsequent reduction of a pyridinium ring
Enantiomerically pure, five membered cyclic nitrones, easily obtained in large amounts from protecte...
Heterocyclic chemistry is of crucial importance as a connection between organic and medicinal chemis...
Chiral 3,4-dibenzyloxy-5-hydroxymethyl-2-thiazolylpyrrolidines under Mitsunobu conditions (R-OH, Ph...
A concise asymmetric synthetic route to two new tetrahydroxyindolizidinone and quinolizidinone deriv...
Benzoquinolizidinone systems were synthesized in both enantiomeric forms from L-glutamic acid. The k...
Concise asymmetric syntheses of (-)-lupinine, (+)-isoretronecanol, (+)-5-epi-tashiromine and (R,R)-1...
The first preparation of enantioenriched phenanthroquinolizidines with a quaternary center at C14a w...
The synthesis of (3S,5S)-quinuclidine-3,5-diol from D-arabinose by two alternative ring closures is ...
International audienceA four-step synthesis of (−)-lentiginosine and its epimers is described starti...
A practical enantioselective protecting group-free four-step route to the key quinolizidinone 6 from...
A summary of recent synthesis approaches to 3,4-dihydroquinoxaline-2-ones is discussed herein along ...
Asymmetric synthesis of indoloquinolizidine has been accomplished by using acyl pyridinium salt bear...
260-263A new route for the synthesis of (R)-glyceraldehyde acetonide via asymmetric dihydroxylation ...
A new strategy for synthesizing quinolizidine skeletons by reductive cyclization via acylpyridinium ...
Synthesis of the title compounds in four steps using inexpensive collidine and lutidine as starting ...
Enantiomerically pure, five membered cyclic nitrones, easily obtained in large amounts from protecte...
Heterocyclic chemistry is of crucial importance as a connection between organic and medicinal chemis...
Chiral 3,4-dibenzyloxy-5-hydroxymethyl-2-thiazolylpyrrolidines under Mitsunobu conditions (R-OH, Ph...
A concise asymmetric synthetic route to two new tetrahydroxyindolizidinone and quinolizidinone deriv...
Benzoquinolizidinone systems were synthesized in both enantiomeric forms from L-glutamic acid. The k...
Concise asymmetric syntheses of (-)-lupinine, (+)-isoretronecanol, (+)-5-epi-tashiromine and (R,R)-1...
The first preparation of enantioenriched phenanthroquinolizidines with a quaternary center at C14a w...
The synthesis of (3S,5S)-quinuclidine-3,5-diol from D-arabinose by two alternative ring closures is ...
International audienceA four-step synthesis of (−)-lentiginosine and its epimers is described starti...
A practical enantioselective protecting group-free four-step route to the key quinolizidinone 6 from...
A summary of recent synthesis approaches to 3,4-dihydroquinoxaline-2-ones is discussed herein along ...
Asymmetric synthesis of indoloquinolizidine has been accomplished by using acyl pyridinium salt bear...
260-263A new route for the synthesis of (R)-glyceraldehyde acetonide via asymmetric dihydroxylation ...
A new strategy for synthesizing quinolizidine skeletons by reductive cyclization via acylpyridinium ...
Synthesis of the title compounds in four steps using inexpensive collidine and lutidine as starting ...
Enantiomerically pure, five membered cyclic nitrones, easily obtained in large amounts from protecte...
Heterocyclic chemistry is of crucial importance as a connection between organic and medicinal chemis...
Chiral 3,4-dibenzyloxy-5-hydroxymethyl-2-thiazolylpyrrolidines under Mitsunobu conditions (R-OH, Ph...
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