The preferred all-gauche conformations in 3-fluoro-1,2-propanediol.
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Catalytic enantioselective addition of organoboron reagents to fluoroketones controlled by electrostatic interactions.Intramolecular OH⋅⋅⋅Fluorine Hydrogen Bonding in Saturated, Acyclic Fluorohydrins: The γ-Fluoropropanol Motif.A halogen bond does not dictate the conformational preferences of cis-1,3-disubstituted cyclohexanes.Is the bioconformation of 5-deoxy-5-fluoro-d-xylulose affected by intramolecular hydrogen bonds?
P2860
The preferred all-gauche conformations in 3-fluoro-1,2-propanediol.
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name
The preferred all-gauche conformations in 3-fluoro-1,2-propanediol.
@en
The preferred all-gauche conformations in 3-fluoro-1,2-propanediol.
@nl
type
label
The preferred all-gauche conformations in 3-fluoro-1,2-propanediol.
@en
The preferred all-gauche conformations in 3-fluoro-1,2-propanediol.
@nl
prefLabel
The preferred all-gauche conformations in 3-fluoro-1,2-propanediol.
@en
The preferred all-gauche conformations in 3-fluoro-1,2-propanediol.
@nl
P2093
P2860
P356
P1476
The preferred all-gauche conformations in 3-fluoro-1,2-propanediol.
@en
P2093
Claudimar J Duarte
Josué M Silla
Laize A F Andrade
P2860
P304
P356
10.1039/C3OB41207E
P577
2013-09-02T00:00:00Z