<p>(a) Pd(PPh<sub>3</sub>)<sub>4</sub>, Na<sub>2</sub>CO<sub>3</sub>, toluene, EtOH, H<sub>2</sub>O, 100°C, 18h; (b) CH<sub>2</sub>Cl<sub>2</sub>, BBr<sub>3</sub>, −78°C to rt.</p
<p>i) Piperidine, EtOH, reflux, 6h, ii) DIBAL-H, Et2O, N2, r.t, iii) Neat SOCl2, reflux, 6h, iv) DEM...
<p>Reagents and conditions: (a) benzyl alcohol, 110 <sup>o</sup>C; (b) NH<sub>4</sub>OH, H<sub>2</su...
<p>Reagents and conditions: (i) Et<sub>3</sub>N, CH<sub>2</sub>Cl<sub>2</sub>, room temperature, ove...
<p>Reagents and conditions: a. NaBH<sub>4</sub>, MeOH; b. PBr<sub>3</sub>, pyridine, 0°C; c. P(OEt)<...
<p>Synthesis scheme of aldehyde <b>6</b>: <i>i)</i> Pd(PPh<sub>3</sub>)<sub>2</sub>Cl<sub>2</sub>, N...
<p>Reagents and conditions: (a) conc. HCl, ZnCl<sub>2</sub>, HCHO(37% in H<sub>2</sub>O); (b) substi...
<p>(a) Pd(OAc)<sub>2</sub>, morpholine, Cs<sub>2</sub>CO<sub>3</sub>, (2-Biphenyl)di-tert-butyl phos...
<p>Synthesis of <i>N</i>-phenylpyrazolyl-<i>N</i>-glycinyl-hydrazone derivatives 4a–h.</p
Synthesis of substituted rhodanine derivatives 9 a–e: i. Pd(PPh3)2Cl2, Na2CO3, DMF/EtOH, RT, 1h; ii....
<p><i><sup>a</sup></i>Reagents and conditions: a) Tosylmethylisocyanate, Na<sub>2</sub>CO<sub>3</sub...
A facile one-step synthesis of naturally occurring magnolol under a mild condition was attain-able b...
<p>Reagents and conditions: i) Hydrazine sulphate, H<sub>2</sub>O, 100°C; ii) Pyridin-4-ylboronic ac...
<p>For residues R<sup><b>1</b></sup>-R<sup><b>5</b></sup> refer to <a href="http://www.plosone.org/a...
<p>Reagents and conditions: (a) 2-phenylethanol for 9a, 3-phenyl-1-propanol for 9b, 110 <sup>o</sup>...
<p>Reagents and Conditions: (a) Ethyl 3-bromobutyrate, Cs<sub>2</sub>CO<sub>3</sub>, MeCN, reflux, 2...
<p>i) Piperidine, EtOH, reflux, 6h, ii) DIBAL-H, Et2O, N2, r.t, iii) Neat SOCl2, reflux, 6h, iv) DEM...
<p>Reagents and conditions: (a) benzyl alcohol, 110 <sup>o</sup>C; (b) NH<sub>4</sub>OH, H<sub>2</su...
<p>Reagents and conditions: (i) Et<sub>3</sub>N, CH<sub>2</sub>Cl<sub>2</sub>, room temperature, ove...
<p>Reagents and conditions: a. NaBH<sub>4</sub>, MeOH; b. PBr<sub>3</sub>, pyridine, 0°C; c. P(OEt)<...
<p>Synthesis scheme of aldehyde <b>6</b>: <i>i)</i> Pd(PPh<sub>3</sub>)<sub>2</sub>Cl<sub>2</sub>, N...
<p>Reagents and conditions: (a) conc. HCl, ZnCl<sub>2</sub>, HCHO(37% in H<sub>2</sub>O); (b) substi...
<p>(a) Pd(OAc)<sub>2</sub>, morpholine, Cs<sub>2</sub>CO<sub>3</sub>, (2-Biphenyl)di-tert-butyl phos...
<p>Synthesis of <i>N</i>-phenylpyrazolyl-<i>N</i>-glycinyl-hydrazone derivatives 4a–h.</p
Synthesis of substituted rhodanine derivatives 9 a–e: i. Pd(PPh3)2Cl2, Na2CO3, DMF/EtOH, RT, 1h; ii....
<p><i><sup>a</sup></i>Reagents and conditions: a) Tosylmethylisocyanate, Na<sub>2</sub>CO<sub>3</sub...
A facile one-step synthesis of naturally occurring magnolol under a mild condition was attain-able b...
<p>Reagents and conditions: i) Hydrazine sulphate, H<sub>2</sub>O, 100°C; ii) Pyridin-4-ylboronic ac...
<p>For residues R<sup><b>1</b></sup>-R<sup><b>5</b></sup> refer to <a href="http://www.plosone.org/a...
<p>Reagents and conditions: (a) 2-phenylethanol for 9a, 3-phenyl-1-propanol for 9b, 110 <sup>o</sup>...
<p>Reagents and Conditions: (a) Ethyl 3-bromobutyrate, Cs<sub>2</sub>CO<sub>3</sub>, MeCN, reflux, 2...
<p>i) Piperidine, EtOH, reflux, 6h, ii) DIBAL-H, Et2O, N2, r.t, iii) Neat SOCl2, reflux, 6h, iv) DEM...
<p>Reagents and conditions: (a) benzyl alcohol, 110 <sup>o</sup>C; (b) NH<sub>4</sub>OH, H<sub>2</su...
<p>Reagents and conditions: (i) Et<sub>3</sub>N, CH<sub>2</sub>Cl<sub>2</sub>, room temperature, ove...
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