7315-68-6

Usage

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

Upstream product

• 451-40-1 phenyl benzyl ketone 
• 20621-69-6 2-cyano-3-methyl-4-phenyl-butyric acid ethyl ester 
• 7315-67-5 3-methyl-4-oxo-4-phenylbutanoic acid 
• 13881-14-6 3-methyl-4-phenylbutanal 
• 64-17-5 ethanol 
• 6052-53-5 3-Methyl-4-phenyl-3-butensaeure 
• 10034-85-2 hydrogen iodide 
• 64-19-7 acetic acid 
• 2114-00-3 2-bromo-1-phenyl-1-propanone 
• 64-18-6 formic acid 
• 3290-53-7 2-methyl-1-phenyl-2-propene 
• 1864-94-4 phenyl formate 
• 103-79-7 1-phenyl-acetone 
• 53852-50-9 3-methyl-4-phenylbut-2-enenitrile 

Downstream Products

• 72277-22-6 3-Methyl-4-phenyl-butansaeure-ethylester 
• 69573-51-9 3-Methyl-4-phenylbutansaeure-methylester 
• 20568-06-3 4,5-dihydro-4-methyl-5-phenyl-2(3H)-furanone 
• 138816-37-2 trans-4-methyl-5-phenylpyrrolidin-2-one 
• 7315-70-0 6-Benzyl-2-methyl-heptanon-⁽⁴⁾ 
• 7315-71-1 6-Benzyl-2-methyl-heptanol-⁽⁴⁾ 
• 13615-40-2 3-methylnaphthalen-1-ol 
• 85268-97-9 2,4-dimethyl-5-phenyl-2-pentanol 
• 85268-66-2 1,2,3,4-tetrahydro-1,1,3-trimethylnaphtalene 
• 14944-23-1 3-methyl-1-tetralone 
• 7315-69-7 3-methyl-4-phenyl-butyryl chloride 

Relevant academic research and scientific papers

An atom-economic approach to carboxylic acids via Pd-catalyzed direct addition of formic acid to olefins with acetic anhydride as a co-catalyst

An effective Pd-catalyzed hydrocarboxylation of olefins using formic acid with acetic anhydride as a co-catalyst is described. A variety of carboxylic acids are obtained in good yields with high regioselectivities under mild reaction conditions without the use of toxic CO gas.

Facile palladium-catalyzed hydrocarboxylation of olefins without external CO gas

An effective Pd-catalyzed hydrocarboxylation of olefins with phenyl formate and formic acid is described. A variety of carboxylic acids are obtained in good yields with high regioselectivities under operationally simple conditions without the use of toxic CO gas.

NAPHT- 2 -YLACETIC ACID DERIVATIVES TO TREAT AIDS

The invention provides compounds of formula (I): or a salt thereof as described herein. The invention also provides pharmaceutical compositions comprising a compound of formula I, processes for preparing compounds of formula (I), intermediates useful for preparing compounds of formula I and therapeutic methods for treating the proliferation of the HIV virus, treating AIDS or delaying the onset of AIDS or ARC symptoms in a mammal using compounds of formula (I).

Design, synthesis, structure, and dehydrogenation reactivity of a water soluble o-iodoxybenzoic acid derivative bearing a trimethylammonium group

5-Trimethylammonio-1, 3-dioxo-1, 3-dihydro-1λ5-benzo[d][1, 2]iodoxol-1-ol anion (AIBX 1a), an o-iodoxybenzoic acid (IBX) derivative having the trimethylammonium moiety on its phenyl ring, possesses very good solubility in water and distinct oxidative properties from IBX, which is demonstrated in the oxidation of various β-keto esters to the corresponding dehydrogenated products using water as cosolvent. The regeneration of AIBX 1a can be easily realized from the reaction mixture due to its good water solubility.2011 American Chemical Society.

Synthese de methoxycarbonylindenes, dihydro-1,2 naphtalenes et benzocycloheptene. Obtention des indanones-1, des tetralones-1 et de la benzosuberone correspondantes

The synthesis of methoxycarbonylindenes, 1,2-dihydro-naphtalenes, and benzocycloheptene starting from the corresponding 1-indanones, 1-tetralones, and benzosuberone is reported.The starting ketones were synthesized by methods described in the literature which were optimized; in some cases new processes are described.