Results 11 to 20 of about 85,474,312 (231)

SYNTHESIS OF 4-(1-BENZYL-5-IMIDAZOLYL)-1,4-DIHYDROPYRIDINES [PDF]

open access: yesJournal of Sciences, Islamic Republic of Iran, 2002
The o-nitrophenyl group at position 4 of dihydropyridine of nifedipine analogues was replaced with 2-alkylthio-1-benzyl-5-imidazolyl substituent. Starting from dihydroxyacetone 2-alkythio-1-benzyl- 5-formyl imidazole (3) was first synthesized which was ...
doaj   +2 more sources

Novel 1, 4-dihydropyridines for L-type calcium channel as antagonists for cadmium toxicity. [PDF]

open access: yesSci Rep, 2017
AbstractThe present study, we design and synthesize the novel dihydropyridine derivatives, i.e., 3 (a-e) and 5 (a-e) and evaluated, anticonvulsant activity. Initially due to the lacuna of LCC, we modeled the protein through modeller 9.15v and evaluated through servers.
Saddala MS   +4 more
europepmc   +7 more sources

REACTIONS OF DIHYDROPYRIDINES WITH BENZYNE [PDF]

open access: yesJournal of Sciences, Islamic Republic of Iran, 1998
Reactions of 1 ,Zdihydropyridines (la-c) and 1,4-dihydropyridines (2a-c) in the presence of benzyne (3) under thermal conditions, and in the case of (2c) under photochemical conditions, have been investigated.
doaj   +1 more source

A Facile Transformation of Amino acids into 1,4-dihydropyridines and their Crystallographic Analysis [PDF]

open access: yes, 2021
A facile transformation of amino acids into substituted 1,4-dihydropyridines (1,4-DHP) is reported. The natural amino acids were converted into gamma-amino beta-keto esters and used for the synthesis of substituted 1,4-dihydropyridines from the ...
Anindita, Adak, Puneeth , Koppal
core   +2 more sources

Visible-Light-Promoted Trifluoromethylthiolation and Trifluoromethylselenolation of 1,4-Dihydropyridines

open access: yes, 2022
We report a metal-free trifluoromethylthiolation and trifluoromethylselenolation of 1,4-dihydropyridines with S-(trifluoromethyl) 4-methylbenzenesulfonothioate and Se-(trifluoromethyl) 4-methylbenzenesulfonoselenoate under visible light irradiation. This
Enxue Chen (14303621)   +11 more
core   +1 more source

Transition-Metal-Free Alkylation and Acylation of Benzoxazinones with 1,4-Dihydropyridines

open access: yes, 2021
The direct functionalization of N-heterocycles is a vital transformation for the development of pharmaceuticals, functional materials, and other chemical entities.
Prithwish Ghosh (7122755)   +13 more
core   +2 more sources

Cobalt-Catalyzed Selective Dearomatization of Pyridines to N–H 1,4-Dihydropyridines

open access: yes, 2022
Catalytic reduction of pyridines to N–H 1,4-dihydropyridines is exceptionally challenging because they are essential intermediates to form tetrahydropyridines.
Lan Liu (88052)   +15 more
core   +1 more source

Direct photolysis of 4-tert-alkyl-1,4-dihydropyridines under blue-light irradiation for the generation of tertiary alkyl radicals [PDF]

open access: yes, 2022
Herein, we disclose a direct photolysis approach for the generation of tertiary alkyl radicals from 4-tert-alkyl-1,4-dihydropyridines (DHPs) under blue LED irradiation, as exemplified in a photochemical Giese reaction.
Spencer, Pitre, Prasadi, Gallage
core   +2 more sources

PHOTODEGRADATION OF 1, 4-DIHYDROPYRIDINE ANTIHYPERTENSIVE DRUGS: AN UPDATED REVIEW

open access: yesInternational Journal of Pharmacy and Pharmaceutical Sciences, 2018
1, 4-dihydropyridine calcium channels blockers (DHPs) are the most commonly used antihypertensive drugs. Unfortunately, these compounds have a significant degradability to light. The oxidation to the pyridine derivative represents the first, and in many cases the only, step of the degradation mechanism.
MICHELE DE LUCA   +3 more
openaire   +4 more sources

Synthesis of Monofluoroalkenes through Visible-Light-Promoted Defluorinative Alkylation of gem-Difluoroalkenes with 4‑Alkyl-1,4-dihydropyridines

open access: yes, 2020
In this study, a facile and efficient method to synthesize monofluoroalkenes by photoredox catalytic defluorinative alkylation of gem-difluoroalkenes with 4-alkyl-1,4-dihydropyridines under mild conditions (room temperature) is described.
Jing Sun (141206)   +6 more
core   +1 more source

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