4-methoxyphenyl 2-propenyl

CN [3p,16 3,17a,18P(jE),20a]-18-[[3-(4-hydroxy-3-methoxyphenyl)-l-oxo-2 propenyl]oxy]-l 1,17-dimethoxyyohimban-16-carboxylic acid methyl ester... [Pg.1799]

C23H30O7 133991-63-6) see Loteprednol etabonate (3p,16p,17a,18p,20a)-18-[[3-I4-t(ethoxycarbonyl)oxy]-3-methoxyphenyl)-l-oxo-2-propenyl]oxy]-ll,17-dimeth-oxyyohimban-16-carboxylic acid methyl ester (C3ftH42N20(o 49806-34-0) see Rescimetol AT-(l-ethoxycarbonyI-3-phenylpropyl)-L-alanine (C,, H 3N04) see Quinapril hydrochloride A7-[l(5)-ethoxycarbonyl-3-phenylpropyl]-L-alanine (C,gH2 N04 82717-962) see Imidapril Moexipril Quinapril hydrochloride Spirapril Trandolapril A -[l(5)-ethoxycarbonyl-3-phenylpropyl]-L-aIanine benzo-thiazol-2-yIthio ester... [Pg.2373]

Hydroxy-1 - (4-hydroxy-3 -methoxyphenyl) -2-[4-(3-hydroxy-l-(E)-propenyl)-2,6-dimethoxyphenoxy] propyl-P-D-glucopyranoside PhOO i4... [Pg.439]

The characteristics of the 1,3-dipolar cycloaddition mechanism of azides and other 1,3-dipoles (such as diazoalkanes, azo-methine imines, nitrones, nitrile imines, nitrile oxides) have been described in detail by Huisgen.191 19 According to the author, the addition of a 1,3-dipole (a b c) to a dipolarophile (d e) occurs by a concerted mechanism in which the two new a bonds are formed simultaneously although not necessarily at equal rates (32). As a consequence, a stereoselective cis addition is observed. Thus, the addition of p-methoxyphenyl azide to dimethyl fiynarate (33) yields l-(p-methoxyphenyl)-4,5-froiw-dicarbomethoxy-AMriazoline (34),194 and 4-nitrophenyl azide gives exclusively the respective cis-addition products 35 and 36 on addition to irons- and cis-propenyl propyl ether.196... [Pg.9]

N1 - PYRROLIDINE, l-( 2-(p-( 3-(p-METHOXYPHENYL)-2-PHENYL-l-PROPENYL)PHENOXY )ETHYD-... [Pg.190]

HYOROXY-3-METHOXYPHENYL J-l-OXO-2-PROPENYL)OXY)-11,17-0IMETHOXY-. METHYL ESTER,... [Pg.222]

Erythro-1-(4 -hydroxy-3 -methoxyphenyl)-2-(2" -methoxy-4"-(T"-(E-)-propenyl) phenoxy-propan-1-ol... [Pg.179]

The first intermolecular C-N bond-forming reactions between substituted 2-bromopyrroles 1450 and 1453 with primary (Tpropanamine, 2-methoxy-l-ethanamine, (4-methoxyphenyl)methanamine, cyclopropanamine, cyclobuta-namine), and cyclic secondary amines (pyrrolidine, morpholine, 1-methylpiperazine, ethyl tetrahydro-l(27/)-pyrazi-necarboxylate, 1-phenylpiperazine, l-(3-phenyl-2-propenyl)piperazine) 1451 were performed using Pd2(dba)3 as catalyst with BINAP as the ligand. The aminations proceeded in the presence of Bu ONa at 80-100 °C in 31-93% yields (Equations 301 and 302) <2004TL769>. However, when the above optimized conditions were applied to the coupling reaction of pyrrole 1450 and acyclic secondary amines such as di- -butylamine, diphenylamine and dipropenylamine, no reaction was observed. [Pg.243]

SYNS ACINTENE O ANETHOLE (FCC) ANISE CAMPHOR ARIZOLE FEMA No. 2086 ISOESTRAGOLE p-METHOXY 3-METHYLSTYRENE l-(p-METHOXYPHENYL)PROPENE l-METHOXY-4-PROPENYLBENZENE 4-METHOXYPROPENYL-BENZENE MONASIRUP NAUU GUM OIL of ANISEED p-l-PROPENYLANISOLE 4-PROPENYL-ANISOLE p-PROPENYLPHENYL METHYL ETHER... [Pg.1181]

Tris[trimethylsilyl]methyl tellurium iodide reacted with phenylmagnesium bromidebutyl tellurium bromide with vinyl magnesium bromide, vinyl tellurium iodide with butyl and 4-methoxyphenyl magnesium bromide, and 2-propenyl tellurium iodide with 4-methoxyph-enyl magnesium bromide to give the expected unsymmetric dialkyl or alkyl aryl tellurium compounds. [Pg.251]

E)-Anethol (E)-Anethole 4-06-00-03796 (Beilstein Handbook Reference) Anethole Anethole, trans- Anisole, p-propenyl-, (E)- Anisole, p-propenyl-, trans- Benzene, 1-methoxy-4-(1-propenyl)-, (E)- BRN 0636190 CCRIS 2481 EINECS 224-062-0 FEMA No. 2086 Methoxy-p-methylstyrene, trans-p- 1-Methoxy-4-(1-propenyljbenzene, (E)- 1-p-Methoxyphenylpropene, trans- NSC 209529 Propenylanisole, p-, (E)- lrans-1-( Methoxyphenyl)-1-propene trans-1-(p-Methoxyphenyl)-1-propene trans-p-Methoxy-p-methylstyrene. Liquid mp = 21,35" bp = 234", bpi2 = 115° d = 0,9882 Xm = 259 nm (cyclohexane) slightly soluble In H2O, soluble... [Pg.39]

Kelly and Lang °" found cyclization of an a-haloketone with amides to be a useful strategy for preparing model oxazoles for the synthesis of dimethyl-sulfomycinate. Refluxing 2-(bromoacetyl)pyridine with methacrylamide or 4-methoxybenzamide gave 2-(2-propenyl)-4-(2-pyridyl)oxazole 201 and 2-(4-methoxyphenyl)-4-(2-pyridyl)oxazole 202 (Scheme 1.55). [Pg.42]

Synonyms trans-Anethol p-Anethole trans-Anise camphor Anisole, p-propenyl-, (E) Anisole, p-propenyl-, trans-Benzene, 1-methoxy-4-(1-propenyl)-, (E)- trans-p-Methoxy-P-methylstyrene trans-1 -(p-Methoxyphenyl) propene (E)-1-Methoxy-4-(1-propenyl) benzene trans-1-Methoxy-4-(1-propenyl) benzene... [Pg.305]

Synonyms Aceteugenol 1-Acetoxy-2-methoxy-4-allylbenzene 3-(4-Acetoxy-3-methoxyphenyl) propene Acetyl eugenol 4-Allyl-2-methoxyphenyl acetate Eugenol acetate 1,3,4-Eugenol acetate 4-(2-Propenyl)-2-methoxyphenyl ethanoate Empirical C12H14O3... [Pg.1788]

Eugenyl methyl ether. See Methyl eugenol Eugenyl phenylacetate CAS 10402-33-2 EINECS/ELINCS 233-868-6 Synonyms 4-Allyl-2-methoxyphenyl phenylacetate Eugenol phenylacetate 4-(2-Propenyl)-2-methoxyphenyl phenylacetate Empirical CisHisOs Properties M.w. 282.34 Toxicology TSCA listed Uses Fragrance in cosmetics Manuf./Distrib. Advanced Synthesis Tech. http //www.advancedsynthesis.com... [Pg.1788]

Propenoic acid, homopolymer, ammonium salt. See Ammonium polyacrylate 2-Propenoic acid, homopolymer, sodium salt. See Sodium polyacrylate 2-Propenoic acid, 2-hydroxyethyl ester. See 2-Hydroxyethyl acrylate 2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-. See Ferulic acid 2-Propenoic acid-2-(hydroxymethyl)-2-(((1 -oxo-2-propenyl) oxy) methyl)-1,3-propanediyl ester. See Pentaerythrityl triacrylate 2-Propenoic acid, 3-(2-hydroxyphenyl)-, (E)-. [Pg.3723]

Propenyl)-2-methoxyphenyl formate 4-(2-Propenyl)-2-methoxyphenyl methanoate. See Eugenyl formate... [Pg.3725]

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