Detalles de la búsqueda
1.
Synthesis of 3-sulfenylindole derivatives from 4-hydroxy-2H-chromene-2-thione and indole using oxidative cross-dehydrogenative coupling reaction and anti-proliferative activity study of some of their sulfone derivatives.
Bioorg Chem
; 141: 106900, 2023 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-37813073
2.
Synthetic utility of biomimicking vanadium bromoperoxidase and n-tetrabutylammonium tribromide (TBATB) in organic synthesis.
Org Biomol Chem
; 20(13): 2562-2579, 2022 03 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-35274638
3.
An environmentally benign regioselective synthesis of 2-benzyl-4-arylquinoline derivatives using aryl amines, styrene oxides and aryl acetylenes.
Org Biomol Chem
; 19(40): 8772-8782, 2021 Oct 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-34591056
4.
Metal-free synthesis of quinoline-2,4-dicarboxylate derivatives using aryl amines and acetylenedicarboxylates through a pseudo three-component reaction.
Org Biomol Chem
; 19(32): 7041-7050, 2021 08 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-34341812
5.
Copper(ii) triflate catalyzed three-component reaction for the synthesis of 2,3-diarylquinoline derivatives using aryl amines, aryl aldehydes and styrene oxides.
Org Biomol Chem
; 19(14): 3255-3262, 2021 Apr 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-33885580
6.
Reaction behaviour of arylamines with nitroalkenes in the presence of bismuth(iii) triflate: an easy access to 2,3-dialkylquinolines.
Org Biomol Chem
; 18(9): 1785-1793, 2020 Mar 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-32073090
7.
Newly synthesized 3-sulfenylindole derivatives from 4-hydroxydithiocoumarin using an oxidative cross dehydrogenative coupling reaction (OCDCR): potential lead molecules for antiproliferative activity.
Org Biomol Chem
; 18(21): 4104-4113, 2020 06 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-32432294
8.
Iodine monobromide catalysed regioselective synthesis of 3-arylquinolines from α-aminoacetophenones and trans-ß-nitrostyrenes.
Org Biomol Chem
; 17(2): 347-353, 2019 01 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-30548050
9.
Electronic effect of substituents on anilines favors 1,4-addition to trans-ß-nitrostyrenes: access to N-substituted 3-arylindoles and 3-arylindoles.
Org Biomol Chem
; 16(20): 3760-3770, 2018 05 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-29722779
10.
Camphorsulfonic Acid Catalyzed One-Pot Three-Component Reaction for the Synthesis of Fused Quinoline and Benzoquinoline Derivatives.
J Org Chem
; 82(23): 12416-12429, 2017 12 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29052992
11.
K2CO3 catalyzed regioselective synthesis of thieno[2,3-b]thiochromen-4-one oximes: access to the corresponding amine and nitroso derivatives.
Org Biomol Chem
; 15(26): 5625-5634, 2017 Jul 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-28640318
12.
One-Pot Synthesis and Evaluation of Antileishmanial Activities of Functionalized S-Alkyl/Aryl Benzothiazole-2-carbothioate Scaffold.
J Org Chem
; 81(8): 3149-60, 2016 Apr 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-26999637
13.
Effects of substituents in the beta-position of 1,3-dicarbonyl compounds in bromodimethylsulfonium bromide-catalyzed multicomponent reactions: a facile access to functionalized piperidines.
J Org Chem
; 73(21): 8398-402, 2008 Nov 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-18841917
14.
An oxidative cross-coupling reaction of 4-hydroxydithiocoumarin and amines/thiols using a combination of I2 and TBHP: access to lead molecules for biomedical applications.
Chem Commun (Camb)
; 54(12): 1513-1516, 2018 Feb 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-29364291
15.
Beyond conventional routes, an unprecedented metal-free chemoselective synthesis of anthranilate esters via a multicomponent reaction (MCR) strategy.
Chem Commun (Camb)
; 51(63): 12673-6, 2015 Aug 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-26159632
16.
Synthesis of Unsymmetrical Sulfides and Their Oxidation to Sulfones to Discover Potent Antileishmanial Agents.
ACS Comb Sci
; 17(11): 671-81, 2015 Nov 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-26441303
17.
Effects of inorganic mercury on reproductive performance of mice.
Food Chem Toxicol
; 42(4): 571-7, 2004 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-15019180
18.
Tetrabutylammonium tribromide (TBATB): a mild and efficient catalyst for O-isopropylidenation of carbohydrates.
Carbohydr Res
; 346(5): 673-7, 2011 Apr 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-21333273
19.
VO(acac)(2)/H(2)O(2)/NaI: a mild and efficient combination for the cleavage of dithioacetal derivatives of sugars.
Carbohydr Res
; 346(16): 2629-32, 2011 Nov 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-21982463
20.
Bromodimethylsulfonium bromide (BDMS) mediated dithioacetalization of carbohydrates under solvent-free conditions.
Carbohydr Res
; 345(15): 2139-45, 2010 Oct 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-20817155