P-Anisamide

Sample preparation 100 p,L Plasma -f- 1 p,g p-anisamide -I- 1 mL 500 mM pH 7.4 Na2HP04/KH2P04 buffer + 1 mL ethyl acetate, shake for 10 min, centrifuge at 1300 g for 5 min. Evaporate the supernatant to dryness under reduced pressure, reconstitute the residue in 200 p,L mobile phase, inject a 100 p,L aliquot. 

Clayden, J. and Tchabanenko, K. (2000) Synthesis of ( )-kainic add by dearomatising cyclisation of a lithiated N-benzyl p-anisamide. Chem. Commun., 317-318. 

Anisamide, m54 Anisic acids, m57, m58, m59 Anidisines, m48, m49, m50 Anisole, m55 p-Anisoyl chloride, m60 p-Anisyl alcohol, m61 Anthranilamide, all2 Anthranilic acid, all8 Araboascorbic acid, i61 APDC, p282 Arsanilic acids, all3... 

S (Z)]]-7-[(2-amino-2-carboxyethyl)thio]-2-[[(2,2-dimethylcyclopropyl)carbonyl]amino]-2-heptanoic acid cjs-4-amino-5-chloro-N-[l-[3-(p-fluorophenoxy)propyl]-3-methoxy-4-piperidinyl]-o-anisamide cis-4-amino-5-chloro-N-[l-[3-(4-fluorophenoxy)propyl]-3-methoxy-4-piperidinyl]-2-methoxybenz amide [l-amino-3-[[[2-[(diaminomethylene)amino]-4-thiazolyljmethyl] thio]propylidene]sulfamide 2-amino- l,9-dihydro-9-[(2-hydroxyethoxy)methyl]-6H-purin-6-one l-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-[(2,3-dihydro-l,4-benzodioxin-2-yl)carbonyl]piperazine... 

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