79464-76-9Relevant articles and documents
Intramolecular OH...Fluorine Hydrogen Bonding in Saturated, Acyclic Fluorohydrins: The γ-Fluoropropanol Motif
Linclau, Bruno,Peron, Florent,Bogdan, Elena,Wells, Neil,Wang, Zhong,Compain, Guillaume,Fontenelle, Clement Q.,Galland, Nicolas,Le Questel, Jean-Yves,Graton, Jér?me
supporting information, p. 17808 - 17816 (2015/12/08)
Fluorination is commonly exercised in compound property optimization. However, the influence of fluorination on hydrogen-bond (HB) properties of adjacent functional groups, as well as the HB-accepting capacity of fluorine itself, is still not completely understood. Although the formation of OH...F intramolecular HBs (IMHBs) has been established for conformationally restricted fluorohydrins, such interaction in flexible compounds remained questionable. Herein is demonstrated for the first time - and in contrast to earlier reports - the occurrence of OH...F IMHBs in acyclic saturated γ-fluorohydrins, even for the parent 3-fluoropropan-1-ol. The relative stereochemistry is shown to have a crucial influence on the corresponding h1JOH...F values, as illustrated by syn- and anti-4-fluoropentan-2-ol (6.6 and 1.9 Hz). The magnitude of OH...F IMHBs and their strong dependence on the overall molecular conformational profile, fluorination motif, and alkyl substitution level, is rationalized by quantum chemical calculations. For a given alkyl chain, the "rule of shielding" applies to OH...F IMHB energies. Surprisingly, the predicted OH...F IMHB energies are only moderately weaker than these of the corresponding OH...OMe. These results provide new insights of the impact of fluorination of aliphatic alcohols, with attractive perspectives for rational drug design.
Syntheses of β-resorcylic acid derivatives, novel potato micro-tuber inducing substances isolated from Lasiodiplodia theobromae
Yang,Toshima,Yoshihara
, p. 5377 - 5384 (2007/10/03)
The syntheses of β-resorcylic acid derivatives 1 and 2, isolated from fungus Lasiodiplodia theobromae, and their dimethyl ethers were accomplished. (R)-(-)-1,3-Butanediol was used as a chiral source of the side chain C6-synthon. The dianion of the benzoic acid moiety was alkylated with C6-bromide to give the desired skeleton. Several β-resorcylic acid derivatives including 1 and 2 were synthesized via hydrogenation, lactonization, demethylation and esterification. The (R)-configuration of the stereogenic center in the side chain was proved by this synthesis. It is confirmed that two phenolic hydroxy groups are required for 1 and 2 to exhibit potato micro-tuber inducing activity.
Stereochemistry of carbanions derived from 1,3-dioxanes
Jernigan, Mary T.,Eliel, Ernest L.
, p. 9638 - 9644 (2007/10/02)
Proton abstraction from 4-methyl-1,3-dioxane (1), 2-phenyl-1,3-dioxane (4), 4-phenyl-1,3-dioxane (5), trans-4-methyl-2-phenyl-1,3-dioxane (7), and cis- (12) and trans-2-methyl-4-phenyl-1,3-dioxane (6) by means of BuLi/KO-t-Bu ("Lochmann-Schlosser base") gave the corresponding carbanions as shown by subsequent deuteronation with EtOD. In contrast, attempted proton abstraction from cis-2-phenyl-4-methyl-1,3-dioxane (3) under the same conditions was unsuccessful, as was abstraction from phenylcyclohexane. Competitive experiments showed that abstraction of the equatorial hydrogen from 7 was about 4 times faster than corresponding abstraction from 6 and that abstraction of the equatorial hydrogen in 6 was well over 25 times faster than abstraction of the axial hydrogen in 12. Deuteronation of the 2-phenyl carbanion from 7 gave the trans isomer 8 in a 70:1 or greater ratio. Deuteronation of the carbanion derived from 6 or 12, in contrast, produced the axial and equatorial 4-phenyl compounds 10 and 11 in a ratio of only about 2:1. The preliminary conclusion that the carbanion derived from 2-phenyl-1,3-dioxane is largely pyramidal, similar to that from 2-phenyl-1,3-dithiane,8 whereas the 4-phenyl-1,3-dioxanyl carbanion is planar, similar to the phenylcyclohexyl (benzylic) carbanion,13 was confirmed by 13C NMR study of these carbanions. The ion derived from 4-phenyl-1,3-dioxane is red and shows the large upfield shifts of the ortho and para ring carbons also seen in the phenylcyclohexyl carbanion13 and characteristic of planar benzylic carbanions.12 In contrast, the orange carbanion derived from 2-phenyl-1,3-dioxane (which was very unstable and easily oxidized), to the extent that measurement was possible, showed the smaller upfield para carbon shift characteristic of pyramidal benzylic carbanions.8b,12 It is concluded that, while two adjacent oxygen atoms mildly stabilize equatorial carbanions (presumably inductively), the destabilizing effect of antiperiplanar lone pairs prevents the 2-phenyl carbanion from becoming planar and inhibits abstraction of the axial hydrogen in compound 3. Reprotonation of the pyramidal ion is stereoselective from the equatorial side. In contrast, in the 4-phenyl carbanion, benzylic resonance stabilization overrides the antiperiplanar effect of one neighboring oxygen atom: Both axial and equatorial hydrogen atoms at C(4) can be abstracted and the carbanion is planar; accordingly reprotonation is essentially nonstereoselective.
