Results 81 to 90 of about 37,838,535 (141)

4-(2-Chloroanilino)-3-phenylfuran-2(5H)-one

open access: yesActa Crystallographica Section E, 2011
The title compound, C16H12ClNO2, featuring a furan-2(5H)-one (γ-butyrolactone) core, contains two molecules (A and B) in the asymmetric unit, with different dihedral angles between the central ring and the pendant phenyl and chlorobenzene rings [
Zhu-Ping Xiao   +4 more
doaj   +1 more source

Tuberostemoamide hemihydrate

open access: yesActa Crystallographica Section E, 2011
In the crystal structure of the title compound {systematic name: (1′S,2R,2′R,3′S,6′R)-3′-ethyl-4-methyl-5H-5′-oxa-10′-azaspiro[furan-2,4′-tricyclo[8.3.0.02,6]tridecane]-5,11 ...
Rong-Rong Zhang   +4 more
doaj   +1 more source

A novel protocol for the stereoselective synthesis of variously substituted (Z)-5-ylidene-5H-furan-2-ones

open access: yes, 1998
The Pd(II)- or Ag(I)-catalyzed lactonization of easily available (E)-4- (1-alkynyl)-2-bromopropenoic acids provides (Z)-3-bromo-5-ylidene-5H-furan- 2-ones, 5.
ROSSI, RENZO   +5 more
core   +1 more source

EXTRACT OF BARBERRY AS ENTIRELY GREEN CATALYST FOR THE SYNTHESIS OF STRUCTURALLY DIVERSE 3,4,5-SUBSTITUTED FURAN-2(5H)-ONES [PDF]

open access: yes, 2016
An eco-friendly and environmentally benign synthesis of 3,4,5-substituted furan-2(5H)-ones employing Iranian seedless barberry, known as Zereshk, (Berberis integerrima “Bidaneh”, Berberidaceae) as a biocatalyst, was developed.
Mojtaba Lashkari   +4 more
core   +1 more source

Synthesis of 4-aryl-3-bromo-5-arylidenefuran-2(5H)-ones rubrolides analogues [PDF]

open access: yes, 2009
Os γ-alquilidenobutenolídeos correspondem a uma família de produtos naturais que possui um grande número de representantes com diversas atividades biológicas.
Barcelos, Rosimeire Coura
core  

Isolation, characterization and therapeutic potential of a novel furanoid diterpene lactone from Hedychium spicatum rhizomes: Insights into antioxidant, anxiolytic, and circadian rhythm modulating properties

open access: yesPhytomedicine Plus
Background: Hedychium spicatum rhizomes is widely used in ayurvedic medicine and traditional medicine systems around the Himalayas. Purpose: Standardization of Hedychium spicatum rhizome SCFE extract by Identification, Isolation, characterization, and ...
Alok Pratap Singh   +5 more
doaj   +1 more source

SYNTHESIS AND EVALUATION OF ANTIMICROBIAL ACTIVITY OF PHENYL AND FURAN-2-YL[1,2,4] TRIAZOLO[4,3-a]QUINOXALIN-4(5H)-ONE AND THEIR HYDRAZONE PRECURSORS [PDF]

open access: yes, 2009
A variety of 1-(s-phenyl)-[1,2,4]triazolo[4,3-a]quinoxalin-4(5H)-one (3a-3h) and 1-(s-furan-2-yl)-[1,2,4]triazolo[4,3- a]quinoxalin-4(5H)-one (5a-d) were synthesized from thermal annelation of corresponding hydrazones (2a-h) and (4a-d) respectively in ...
Ajani, O. O., Nwinyi, Obinna
core  

Addition reactions of acetylenic esters to 6,7-dihydrobenzo[b]furan-4-(5H)-one, 6,7-dihydroindol-4(5H)-one, 5,6-dihydrobenzo[b]furan-7(6H)-one and 5,6-dihydroindol-7(6H)-one ketoximes. Formation of reduced furo[g]- and pyrrole[g]indoles

open access: yes, 2003
thermal rearrangement of 6,7-dihydrobenzo[b]furan-4(5H)-one and 4,5,6,7-tetrahydroindol-4-one 4(7)-O-(E)-(1.2-dimethoxycarbonylvinyl)ketoximes gave 4,5-dihydrofuro[2,3g]- and 4,5-dihidropyrrolo[2,3g]- and [3,2-g] indoles, three novel tricyclic ...
PIRISI, Maria Antonietta   +3 more
core   +1 more source

Constituintes químicos de Vernonia scorpioides (Lam) Pers. (Asteraceae) Chemical constituents of Vernonia scorpioides (Lam) Pers. (Asteraceae)

open access: yesQuímica Nova, 2013
The chemical investigation of hexane and ethanol extracts from the aerial parts of Vernonia scorpioides resulted in the isolation and characterization of a new polyacetylene lactone, rel-4-dihydro-4β-hydroxy-5a-octa-2,4,6-triynyl-furan-2-(5H)-one ...
Adalva Lopes Machado   +8 more
doaj  

An efficient synthesis of 4,5-dihydronaphtho[2,1-b]furan through a novel ring transformation of 2H-pyran-2-one

open access: yes, 2004
An innovative route for the synthesis of substituted naphtho[2,1-b]furan has been delineated through a ring transformation reaction of suitably functionalized 2H-pyran-2-ones by reaction with 6,7-dihydro-5H-benzofuran-4-one, in good ...
Goel, Atul, Dixit, Manish
core   +1 more source

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