X-Ray crystallography establishes that the marine alkaloids ()-haliclonacyclamine A 1 and (+)-haliclonacyclamine B 2 each have the configuration C2 (R), C3 (R), C7 (R), and C9 (R). The alkaloids appear to be enantiomerically pure; this provides an insight into the stereochemical consequences of the biosynthetic pathway leading to these bioactive 3-alkylpiperidine alkaloids
A tandem Michael addition-enolate alkylation followed by Dieckmann cyclization and Beckmann rearrang...
The absolute configuration of the marine sponge alkaloid pyrinodemin A is established by organic syn...
The conjugate addition of lithium (R)-N-(3-chloropropyl)-N-(α-methylbenzyl)amide to α,β-unsaturated ...
Chemical analysis of an Indonesian sponge sample has provided three new 3-alkylpiperidine alkaloids,...
The enantioselective synthesis (3.7% overall yield in nine steps from 2) and biological screening of...
The marine natural product haliclamide has been synthesized based on macrocyclization by ring-closin...
A new 3-alkylpiperidine compound (-)-acanthocyclamine A (1) has been obtained from the methanolic ex...
Compounds 2-5, incorporating various elements of the 3,4′- bis(piperidine) core associated with the ...
The X-ray crystal structures have been determined for three alkaloids isolated from the bark of the ...
The analysis of the polar extracts of the Pacific sponge Haliclona sp. yielded new dimeric (1), trim...
The halogenated alkaloid chloromethylhalicyclamine B (1), together with the known natural compound h...
The previously assigned 3R configuration of (-)-vasicinone has been reversed and this pyrrolo[2,1-b]...
The <i>syn</i>- and <i>anti</i>-diastereoisomeric forms of the reported structures of the marine alk...
The first total syntheses of (+)-villatamines A and B have been realized in six and five steps, resp...
The conjugate addition of lithium (<i>R</i>)-<i>N</i>-(3-chloropropyl)-<i>N</i>-(α-methylbenzyl)ami...
A tandem Michael addition-enolate alkylation followed by Dieckmann cyclization and Beckmann rearrang...
The absolute configuration of the marine sponge alkaloid pyrinodemin A is established by organic syn...
The conjugate addition of lithium (R)-N-(3-chloropropyl)-N-(α-methylbenzyl)amide to α,β-unsaturated ...
Chemical analysis of an Indonesian sponge sample has provided three new 3-alkylpiperidine alkaloids,...
The enantioselective synthesis (3.7% overall yield in nine steps from 2) and biological screening of...
The marine natural product haliclamide has been synthesized based on macrocyclization by ring-closin...
A new 3-alkylpiperidine compound (-)-acanthocyclamine A (1) has been obtained from the methanolic ex...
Compounds 2-5, incorporating various elements of the 3,4′- bis(piperidine) core associated with the ...
The X-ray crystal structures have been determined for three alkaloids isolated from the bark of the ...
The analysis of the polar extracts of the Pacific sponge Haliclona sp. yielded new dimeric (1), trim...
The halogenated alkaloid chloromethylhalicyclamine B (1), together with the known natural compound h...
The previously assigned 3R configuration of (-)-vasicinone has been reversed and this pyrrolo[2,1-b]...
The <i>syn</i>- and <i>anti</i>-diastereoisomeric forms of the reported structures of the marine alk...
The first total syntheses of (+)-villatamines A and B have been realized in six and five steps, resp...
The conjugate addition of lithium (<i>R</i>)-<i>N</i>-(3-chloropropyl)-<i>N</i>-(α-methylbenzyl)ami...
A tandem Michael addition-enolate alkylation followed by Dieckmann cyclization and Beckmann rearrang...
The absolute configuration of the marine sponge alkaloid pyrinodemin A is established by organic syn...
The conjugate addition of lithium (R)-N-(3-chloropropyl)-N-(α-methylbenzyl)amide to α,β-unsaturated ...