Four indolizidine based alkaloids (IBAs) have been synthesized in a highly enantioselective, straightforward, and flexible manner. As a key step our previously developed Brønsted acid catalyzed vinylogous Mannich reaction was employed which easily afforded gram amounts of an optically pure central intermediate which can be converted into a wide range of diversely substituted IBAs
Enantioselective α-deprotonation-rearrangement of N-Boc hexahydroazonine oxide 10 using organolithiu...
L-Glutamic diethyl ester hydrochloride was converted to its pyrrole derivative 22 by condensation wi...
International audienceThe asymmetric synthesis of trifluoromethyl-piperidine-based g-aminoacids and ...
Four indolizidine based alkaloids (IBAs) have been synthesized in a highly enantioselective, straigh...
Abstract: The use of Vinylogous urethanes as pivotal intermediates m the synthesis of mdolizidine al...
Mannich type reactions of a preformed aldimine with various carbonyl compounds were investigated wit...
Indolizidine 209D (2) was synthesized in 11 steps from L-aspartic acid (3) in an overall yield of 16...
Short routes to enantiomerically pure indolizidine and quinolizidine alkaloids have been developed u...
Indolo[2,3-a]quinolizines have been prepared in enantiomerically pure form by a very short and effic...
Background: Prior work from these laboratories has centred on the development of enaminones as versa...
Quinolizidines, indolizidines and substituted piperidines are ubiquitous structural motifs present i...
The Rh(I)•CKphos catalyzed [2 + 2 + 2] cycloaddition of 1,1-disubstituted alkenyl isocyanates and al...
The enantiogenic syntheses of (-)-indolizidine 167B (1) and (+)-monomorine (2) are described. D-Norv...
The reactions at the C-3 carbonyl group of isatins, by nucleophilic addition or spiroannulation, tra...
AbstractNew Reactions and Synthetic Strategies toward Indolizidine Alkaloids and Pallavicinia Diterp...
Enantioselective α-deprotonation-rearrangement of N-Boc hexahydroazonine oxide 10 using organolithiu...
L-Glutamic diethyl ester hydrochloride was converted to its pyrrole derivative 22 by condensation wi...
International audienceThe asymmetric synthesis of trifluoromethyl-piperidine-based g-aminoacids and ...
Four indolizidine based alkaloids (IBAs) have been synthesized in a highly enantioselective, straigh...
Abstract: The use of Vinylogous urethanes as pivotal intermediates m the synthesis of mdolizidine al...
Mannich type reactions of a preformed aldimine with various carbonyl compounds were investigated wit...
Indolizidine 209D (2) was synthesized in 11 steps from L-aspartic acid (3) in an overall yield of 16...
Short routes to enantiomerically pure indolizidine and quinolizidine alkaloids have been developed u...
Indolo[2,3-a]quinolizines have been prepared in enantiomerically pure form by a very short and effic...
Background: Prior work from these laboratories has centred on the development of enaminones as versa...
Quinolizidines, indolizidines and substituted piperidines are ubiquitous structural motifs present i...
The Rh(I)•CKphos catalyzed [2 + 2 + 2] cycloaddition of 1,1-disubstituted alkenyl isocyanates and al...
The enantiogenic syntheses of (-)-indolizidine 167B (1) and (+)-monomorine (2) are described. D-Norv...
The reactions at the C-3 carbonyl group of isatins, by nucleophilic addition or spiroannulation, tra...
AbstractNew Reactions and Synthetic Strategies toward Indolizidine Alkaloids and Pallavicinia Diterp...
Enantioselective α-deprotonation-rearrangement of N-Boc hexahydroazonine oxide 10 using organolithiu...
L-Glutamic diethyl ester hydrochloride was converted to its pyrrole derivative 22 by condensation wi...
International audienceThe asymmetric synthesis of trifluoromethyl-piperidine-based g-aminoacids and ...