Assignment of relative configuration of desoxypropionates by 1H NMR spectroscopy: method development, proof of principle by asymmetric total synthesis of xylarinic acid A and applications.
about
Structure elucidation of female-specific volatiles released by the parasitoid wasp Trichogramma turkestanica (Hymenoptera: Trichogrammatidae).Identification, Synthesis, and Field Tests of the Sex Pheromone of Margarodes prieskaensis (Jakubski).Stereospecific cross-coupling reactions of aryl-substituted tetrahydrofurans, tetrahydropyrans, and lactones.(7E,11E)-3,5,9,11-Tetramethyltridecadienal: Sex Pheromone of the Strepsipteran Xenos peckii.A highly stereoselective and flexible strategy for the convergent synthesis of long-chain polydeoxypropionates: application towards the synthesis of the glycolipid membrane components hydroxyphthioceranic and phthioceranic acid.Directed hydrogenations and an ireland-claisen rearrangement linked to evans-tishchenko chemistry: the highly efficient total synthesis of the marine cyclodepsipeptide doliculide.
P2860
Assignment of relative configuration of desoxypropionates by 1H NMR spectroscopy: method development, proof of principle by asymmetric total synthesis of xylarinic acid A and applications.
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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name
Assignment of relative configu ...... rinic acid A and applications.
@en
Assignment of relative configu ...... rinic acid A and applications.
@nl
type
label
Assignment of relative configu ...... rinic acid A and applications.
@en
Assignment of relative configu ...... rinic acid A and applications.
@nl
prefLabel
Assignment of relative configu ...... rinic acid A and applications.
@en
Assignment of relative configu ...... rinic acid A and applications.
@nl
P2093
P2860
P356
P1476
Assignment of relative configu ...... rinic acid A and applications.
@en
P2093
Bernhard Breit
Konrad Lehr
Lucie Colas
Yvonne Schmidt
P2860
P304
P356
10.1002/CHEM.201103988
P407
P577
2012-04-27T00:00:00Z