774-44-7

Usage

InChI:InChI=1/C11H14O2/c1-9-7-8-12-11(13-9)10-5-3-2-4-6-10/h2-6,9,11H,7-8H2,1H3

Upstream product

• 18826-95-4 1.3-butanediol 
• 100-52-7 benzaldehyde 
• 6296-95-3 1,1,2-triphenyl-1,2-ethanediol 
• 579-43-1 (1S,2R)-1,2-diphenylethane-1,2-diol 
• 1439-07-2 trans-Stilbene oxide 

Downstream Products

• 90458-77-8 3-(benzyloxy)butanal 
• 136367-86-7 C₂₄H₃₀O₂ 
• 59694-08-5 3-hydroxylbutyl benzoate 
• 80403-62-9 4-hydroxybut-2-yl benzoate 
• 2867-66-5 1-benzoyloxy-3-bromobutane 
• 51591-50-5 3-benzoyloxy-1-bromobutane 
• 65-85-0 benzoic acid 
• 54889-80-4 1,3-dibenzyloxybutane 
• 4799-69-3 4-benzyloxy-2-butanol 
• 52657-84-8 (±)-3-benzyloxybutan-1-ol 
• 167163-46-4 C₁₁H₁₂O₄ 
• 104311-81-1 4-benzoyloxypentanenitrile 
• 72258-23-2 (2R,4S)-4-Methyl-2-phenyl-1,3-dioxan 
• 79464-76-9 (2S,4R)-4-methyl-2-phenyl-1,3-dioxane 

Relevant academic research and scientific papers

Macro-cyclic immuno-modulator

The invention provides a macro-cyclic immuno-modulator, and discloses a compound shown as a formula I, and a tautomer, an enantiomer, a pharmaceutically acceptable salt, a crystal form, hydrate or solvate thereof. Experiment results show that the compound can be effectively combined with STING and has a good STING protein excitation function. Therefore, the compound can be used as an STING agonist, can be used to treat various related diseases, and has a very good application prospect in preparing medicines for treating diseases related to STING activity, especially medicines for treating inflammatory and autoimmune diseases, infectious diseases, cancers or precancerous syndromes.

Intramolecular OH...Fluorine Hydrogen Bonding in Saturated, Acyclic Fluorohydrins: The γ-Fluoropropanol Motif

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.

Chemoselective conversion of aromatic epoxide and 1,2-diol to 1,3-dioxane derivatives with phenyltrimethylammonium tribromide in the presence of a catalytic amount of antimony(III) bromide

trans-Stilbene oxide was oxidatively converted to 2-phenyl-1,3-dioxanes with phenyltrimethylammonium tribromide in the presence of various 1,3-diols and a catalytic amount of SbBr3 in DMSO at room temperature. Aromatic 1,2-diol, such as hydrobenzoin, was similarly converted to 2-aryl-1,3-dioxane derivatives under the same reaction conditions.

Reductive cleavage of acetals and ketals with 9-borabicyclo[3.3.1]nonane

The reductive cleavage of benzaldehyde acetals and acetophenone ketals with the air-stable crystalline 9-borabicyclo[3.3.1]-nonane dimer provides monobenzylated ether derivatives of diols and 1,2-oxygen-transposed β-phenethyl alcohols, respectively. The boron moiety is effectively recovered through simple procedures which involve convenient air-stable reagents and boron byproducts. The process is particularly selective for 1,3-diols giving the more substituted monobenzyl ether derivatives exclusively. With acetophenone ketals both reduction and elimination occur, permitting 9-BBN-H to hydroborate the resulting styrene to produce 1,2-oxygen-transposed β-phenethyl alcohols cleanly. Potential applications of this new process were illustrated with the synthesis of the hallucinogen, mescaline, and the analgesic, ibufenac.

2,4,4,6-Tetrabromo-2,5-cyclohexadienone (TABCO) as a versatile, efficient, and chemoselective catalyst for the acetalization and transacetalization of carbonyl compounds, the preparation of acetonides from epoxides and acylals (1,1-diacetates) from aldehydes

The efficient and chemoselective preparation of acetals and ketals from carbonyl compounds, transacetalization reactions, the conversion of epoxides to acetonides, and the preparation of acylals from aldehydes in the presence of catalytic amounts of 2,4,4,6-tetrabromo-2,5-cyclohexadienone (TABCO) are described.

Stereochemistry of carbanions derived from 1,3-dioxanes

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.