International audienceA short and efficient approach has been designed for the synthesis of new gamma-lactams that feature gem -difluorinated side-chains in position 4. The key steps involve 1,4-addition of nitroalkane anions on electrophilic gem -difluoroalkenes, followed by a cascade nitro reduction-heterocyclization. This flexible strategy also allows easy introduction of substituents in positions 3 or 5
International audienceStarting from easily accessible gem-difluoropropargylic derivatives, a DBU-med...
gamma-Keto thioesters were easily transformed into alpha,beta-unsaturated lactams using a two-step p...
International audienceA variety of 4-substituted ß-lactams can be readily prepared by the radical ad...
International audienceA short and efficient approach has been designed for the synthesis of new gamm...
International audienceNew five-membered cyclic nitrones withgem-difluoroalkyl groups in gamma-positi...
The diastereoselective synthesis of fluorinated δ-lactams has been achieved through an efficient fiv...
The paper presents an efficient and straightforward transformation of alpha,beta-unsaturated gamma-l...
Reported herein is the application of fluoroallylboration for the synthesis of gem-difluorinated com...
A one-pot, three-step tandem process has been developed for the direct synthesis of functionalised b...
A series of 4,5-substituted chiral gamma-lactams were synthesized through a highly diastereoselectiv...
International audienceThe Kinugasa reaction, applied to propargylic gem-difluorides, allows a very d...
cis-4-(1-Chloro-1-methylethyl)-1-(omega-hydroxyalkyl)azetidin-2-ones were diastereoselectively trans...
boronolide; gem-difluoromethylenated analogues; gem-difluoropropargylation; α,β-unsaturated-δ-lacton...
International audienceA new strategy has been designed for the preparation of gem-difluoro-bisarylic...
The synthesis of <i>gem</i>-difluoromethylenated polycyclic cage compounds, utilizing PhSCF<sub>2</s...
International audienceStarting from easily accessible gem-difluoropropargylic derivatives, a DBU-med...
gamma-Keto thioesters were easily transformed into alpha,beta-unsaturated lactams using a two-step p...
International audienceA variety of 4-substituted ß-lactams can be readily prepared by the radical ad...
International audienceA short and efficient approach has been designed for the synthesis of new gamm...
International audienceNew five-membered cyclic nitrones withgem-difluoroalkyl groups in gamma-positi...
The diastereoselective synthesis of fluorinated δ-lactams has been achieved through an efficient fiv...
The paper presents an efficient and straightforward transformation of alpha,beta-unsaturated gamma-l...
Reported herein is the application of fluoroallylboration for the synthesis of gem-difluorinated com...
A one-pot, three-step tandem process has been developed for the direct synthesis of functionalised b...
A series of 4,5-substituted chiral gamma-lactams were synthesized through a highly diastereoselectiv...
International audienceThe Kinugasa reaction, applied to propargylic gem-difluorides, allows a very d...
cis-4-(1-Chloro-1-methylethyl)-1-(omega-hydroxyalkyl)azetidin-2-ones were diastereoselectively trans...
boronolide; gem-difluoromethylenated analogues; gem-difluoropropargylation; α,β-unsaturated-δ-lacton...
International audienceA new strategy has been designed for the preparation of gem-difluoro-bisarylic...
The synthesis of <i>gem</i>-difluoromethylenated polycyclic cage compounds, utilizing PhSCF<sub>2</s...
International audienceStarting from easily accessible gem-difluoropropargylic derivatives, a DBU-med...
gamma-Keto thioesters were easily transformed into alpha,beta-unsaturated lactams using a two-step p...
International audienceA variety of 4-substituted ß-lactams can be readily prepared by the radical ad...