HANTZSCH-TYPE DIHYDROPYRIDINES .4. CARBOXYLIC-ACIDS

[1] BRUICE TC, 1966, BIORGANIC MECHANISMS, V2, P301

[2] CHEMISTRY OF DIHYDROPYRIDINES [J]. CHEMICAL REVIEWS, 1972, 72 (01) : 1 - +

[3] FLORKIN M, 1966, COMPREHENSIVE BIOCHE, V14

[4] HANTZSCH A, 1884, BER, V17, P2903

[5] KUTHAN J, 1964, COLLECT CZECH CHEM C, V29, P1654

[6] LACHOWICZ B, 1896, MONATSH CHEM, V17, P343

[7] DIHYDROPYRIDINES WITH POTENT HYPOTENSIVE ACTIVITY PREPARED BY HANTZSCH REACTION [J]. JOURNAL OF PHARMACY AND PHARMACOLOGY, 1972, 24 (11) : 917 - &

[8] LOEV B, 1974, J MED CHEM, V17, P956, DOI 10.1021/jm00255a010

[9] MACKO E, 1972, ARCH INTERN PHARMACO, V197, P265

[10] MILLS WH, 1924, J CHEM SOC, P2365

[1] BRUICE TC, 1966, BIORGANIC MECHANISMS, V2, P301

[2] CHEMISTRY OF DIHYDROPYRIDINES [J]. CHEMICAL REVIEWS, 1972, 72 (01) : 1 - +

[3] FLORKIN M, 1966, COMPREHENSIVE BIOCHE, V14

[4] HANTZSCH A, 1884, BER, V17, P2903

[5] KUTHAN J, 1964, COLLECT CZECH CHEM C, V29, P1654

[6] LACHOWICZ B, 1896, MONATSH CHEM, V17, P343

[7] DIHYDROPYRIDINES WITH POTENT HYPOTENSIVE ACTIVITY PREPARED BY HANTZSCH REACTION [J]. JOURNAL OF PHARMACY AND PHARMACOLOGY, 1972, 24 (11) : 917 - &

[8] LOEV B, 1974, J MED CHEM, V17, P956, DOI 10.1021/jm00255a010

[9] MACKO E, 1972, ARCH INTERN PHARMACO, V197, P265

[10] MILLS WH, 1924, J CHEM SOC, P2365