A three-component reaction for diversity-oriented synthesis of polysubstituted piperidines: solution and solid-phase optimization of the first tandem aza[4+2]/allylboration.
about
Fluorous mixture synthesis of two libraries with hydantoin-, and benzodiazepinedione-fused heterocyclic scaffolds.Natural products as an inspiration in the diversity-oriented synthesis of bioactive compound libraries.Asymmetric multicomponent reactions (AMCRs): the new frontier.Permuting Diels-Alder and Robinson Annulation Stereopatterns.In Vitro Metabolic Stability and in Vivo Biodistribution of 3-Methyl-4-furoxancarbaldehyde Using PET Imaging in RatsBoron-substituted 1,3-dienes and heterodienes as key elements in multicomponent processes.Allylboration of Carbonyl CompoundsNew 1,3-Disubstituted Enantiomerically Pure Allylboronic Esters by Johnson Rearrangement of Boron-Substituted Allyl Alcohols
P2860
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P2860
A three-component reaction for diversity-oriented synthesis of polysubstituted piperidines: solution and solid-phase optimization of the first tandem aza[4+2]/allylboration.
description
2003 nî lūn-bûn
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name
A three-component reaction for ...... tandem aza[4+2]/allylboration.
@en
A three-component reaction for ...... tandem aza[4+2]/allylboration.
@nl
type
label
A three-component reaction for ...... tandem aza[4+2]/allylboration.
@en
A three-component reaction for ...... tandem aza[4+2]/allylboration.
@nl
prefLabel
A three-component reaction for ...... tandem aza[4+2]/allylboration.
@en
A three-component reaction for ...... tandem aza[4+2]/allylboration.
@nl
P2093
P356
P1476
A three-component reaction for ...... tandem aza[4+2]/allylboration.
@en
P2093
Agnieszka Ulaczyk-Lesanko
Barry B Touré
Hamid R Hoveyda
Jyoti Tailor
P304
P356
10.1002/CHEM.200390049
P407
P577
2003-01-01T00:00:00Z