1992
DOI: 10.1007/bf00475250
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Synthesis of phenyl-substituted derivatives of decahydrophenanthridine-1, 7-dione and hexahydro-8-isoquinolone

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Cited by 2 publications
(2 citation statements)
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“…Heterocyclic compounds that include the 1,4-dihydropyridine fragment in their structure are of great interest to medical chemists [1][2][3] due to their wide range of biological effects. Compounds of this type have antihypertensive, anticonvulsant, antioxidant antibacterial, antiviral, antiviral, spasmolytic, contraceptive activity, without showing a mutagenic effect [4][5][6].…”
Section: Introductionmentioning
confidence: 99%
“…Heterocyclic compounds that include the 1,4-dihydropyridine fragment in their structure are of great interest to medical chemists [1][2][3] due to their wide range of biological effects. Compounds of this type have antihypertensive, anticonvulsant, antioxidant antibacterial, antiviral, antiviral, spasmolytic, contraceptive activity, without showing a mutagenic effect [4][5][6].…”
Section: Introductionmentioning
confidence: 99%
“…Dehydration of bicycles (6 a, b, c) in the presence of acid leads to the formation of pyran ring with the formation of tricycles (7a, b). Interaction of ketodienols with β-enaminones gives new derivatives hexahydroisoquinoline (8a, b, c) and decahydrophenanthridine (7d, e) [13] [14]. It should be noted that currently it has been revealed that there is an effective way to obtain not only acetylcyclohexenone (3b) [15], but also acetylcyclopentenenone (3a) [16] and other related endions [17]- [19] from corresponding cis-β-diketones by their selenenylation followed by selenoxide elimination of with hydrogen peroxide.…”
Section: Introductionmentioning
confidence: 99%