摘要:
Compounds are described of formula ##STR1## in which: Ar represents a aryl, possibly substituted;R represents a C.sub.1 -C.sub.4 alkyl;R' represents a hydroxyl, an alkoxy, an amino group possibly mono or di-alkyl substituted, or an O-M+ group where M+ represents the cation of an alkaline metal;X represents a hydrogen, chlorine, bromine or iodine atom, a hydroxyl, or an acyloxy, alkylsulphonyloxy or arylsulphonyloxy group.The compounds of formula I can be easily transformed into alphaarylalkanoic acids of formula ##STR2## in which Ar and R have the aforesaid meanings.
摘要:
Process for preparing esters of 2-(6'-methoxy-2'-naphthyl)-propionic acids via rearrangement of ketals of 2-iodo-1-(6'-methoxy-2'-naphthyl)-propan-1-one in a protic medium.
摘要:
Alpha substituted alkylarylketals of formula: ##STR1## wherein Ar is an aromatic radical having from 3 to 20 C atoms,X is halogen, OR.sub.3 (wherein R.sub.3 is H, acyl or aroyl), OSO.sub.2 CH.sub.3 or OSO.sub.2 C.sub.6 H.sub.4 --CH.sub.3,R is H or alkyl having from 1 to 3 C atoms,Y is --CH.sub.2 --C(R.sub.1).dbd.C(R.sub.2)--CH.sub.2 --(wherein, in turn, R.sub.1 and R.sub.2 are H or methyl).The products of formula I are useful for preparing alpha-aryl-alkanoic acids.
摘要:
A process is described for preparing optically active alpha-arylalkanoic acids consisting of rearranging an optically active ketal of formula ##STR1## in which the substituents have the meaning given in the description of the invention.
摘要:
Compounds of formula ##STR1## (wherein Ar, R, R.sub.1 and X have the meanings reported in the description) are useful intermediates for the preparation of a variety of organic compounds, also optically active, like alpha-haloketones, alpha-hydroxyketones or ketals, alpha-arylalkanoic acids.
摘要:
Process for preparing esters of aryl alkanoic acids via oxidation of the corresponding ketones with bromine or iodine in the presence of a metal halide and an alcohol.The thus obtained esters are then easily hydrolized to give the corresponding aryl alkanoic acids which are particularly useful as anti-inflammatory, analgesic and anti-pyretic agents.
摘要:
A process is described for the preparation of intermediates useful in the synthesis of Fosfomycin.More particularly, an enantioselective process is described for the preparation of derivatives of (1S,2S)-1,2-dihydroxypropyl-phosphonic acid of formula ##STR1## wherein R.sub.2 and R.sub.3 have the meanings reported in the specification.
摘要:
Rearrangement of alpha-halo-alkylarylketals in neutral or weakly alkaline conditions and in the presence of a polar-protic medium and subsequent hydrolysis of the thus obtained esters, in the same reaction medium, to afford the corresponding alpha-arylalkanoic acids or their salts which are particularly useful as anti-inflammatory, analgesic and antipyretic agents.
摘要:
A process for the preparation of clopidogrel (1) by reaction of the N,N′-bis-4,5,6,7-tetrahydro-[3,2-c]-thienopyridyl methane (12) with (R)-2-chlorophenylacetic acid derivatives of formula (13) in which X and R have the meanings as indicated in the disclosure.