PREPARATION OF 3-PYRIDOLS FROM FURANS

[1] THE PREPARATION OF RANEY NICKEL CATALYSTS AND THEIR USE UNDER CONDITIONS COMPARABLE WITH THOSE FOR PLATINUM AND PALLADIUM CATALYSTS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1948, 70 (02) : 695 - 698

[2] ADKINS H, 1942, ORGANIC CHEM, P810

[3] PREPARATION OF CIS AND TRANS 2,5-DIMETHOXY-2-(ACETAMIDOMETHYL)-2,5-DIHYDROFURAN, OF CISS AND TRANS 2,5-DIMETHOXY-2-(ACETAMIDOMETHYL)-TETRAHYDROFURAN AND OF 1-PHENYL-2-(ACETAMIDOMETHYL)-PYRROLE [J]. ACTA CHEMICA SCANDINAVICA, 1952, 6 (05): : 667 - 670

[4] CLAUSONKAAS N, 1947, KGL DANSKE VIDENSKAB, V24, P6

[5] The urea dearrangement II [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1923, 45 : 1816 - 1820

[6] Concerning a few substituted beta-positions in alpha-picoline. [J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1940, 73 : 78 - 80

[7] FISCHER O, 1884, BER, V17, P755

[8] HARTMAN WW, 1943, ORG SYNTH, V2, P278

[9] Catalytic reduction of nitriles and oximes [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1928, 50 : 3370 - 3374

[10] KAO CH, 1948, J CHEM ENG CHINA, V15, P80

[1] THE PREPARATION OF RANEY NICKEL CATALYSTS AND THEIR USE UNDER CONDITIONS COMPARABLE WITH THOSE FOR PLATINUM AND PALLADIUM CATALYSTS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1948, 70 (02) : 695 - 698

[2] ADKINS H, 1942, ORGANIC CHEM, P810

[3] PREPARATION OF CIS AND TRANS 2,5-DIMETHOXY-2-(ACETAMIDOMETHYL)-2,5-DIHYDROFURAN, OF CISS AND TRANS 2,5-DIMETHOXY-2-(ACETAMIDOMETHYL)-TETRAHYDROFURAN AND OF 1-PHENYL-2-(ACETAMIDOMETHYL)-PYRROLE [J]. ACTA CHEMICA SCANDINAVICA, 1952, 6 (05): : 667 - 670

[4] CLAUSONKAAS N, 1947, KGL DANSKE VIDENSKAB, V24, P6

[5] The urea dearrangement II [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1923, 45 : 1816 - 1820

[6] Concerning a few substituted beta-positions in alpha-picoline. [J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1940, 73 : 78 - 80

[7] FISCHER O, 1884, BER, V17, P755

[8] HARTMAN WW, 1943, ORG SYNTH, V2, P278

[9] Catalytic reduction of nitriles and oximes [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1928, 50 : 3370 - 3374

[10] KAO CH, 1948, J CHEM ENG CHINA, V15, P80