Academic literature on the topic 'Cinnamoyl chloride'

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Cinnamoyl chloride.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Cinnamoyl chloride"

1

D'Souza, Malcolm J., Anthony M. Darrington, and Dennis N. Kevill. "On the Importance of the Aromatic Ring Parameter in Studies of the Solvolyses of Cinnamyl and Cinnamoyl Halides." Organic Chemistry International 2010 (June 29, 2010): 1–9. http://dx.doi.org/10.1155/2010/130506.

Full text
Abstract:
In solvolysis studies using Grunwald-Winstein plots, dispersions were observed for substrates with aromatic rings at the α-carbon. Several examples for the unimolecular solvolysis of monoaryl benzylic derivatives and related diaryl- or naphthyl-substituted derivatives have now been reported, where the application of the aromatic ring parameter (I) removes this dispersion. A recent claim suggesting the presence of an appreciable nucleophilic component to the I scale has now been shown, in a review of the solvolysis of highly-hindered alkyl halides, to be unlikely to be correct. Attention is now
APA, Harvard, Vancouver, ISO, and other styles
2

Bejblová-Voláková, M., J. Vlk, and D. Procházková. "Acylation of Ferrocene with Adamantoyl Chloride and Cinnamoyl Chloride." Topics in Catalysis 53, no. 19-20 (2010): 1411–18. http://dx.doi.org/10.1007/s11244-010-9601-x.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Schildknecht, Hermann, Horst Sauer та Peter Kunzelmann. "Pflanzenabwehrstoffe XXXIV [1]. Synthese der 2-(E)-O-(4-Hydroxy-cinnamoyI)-ᴅ,ʟ-galactarsäure, eines vermeintlich photosensitiven Faktors aus Glycine max / Synthesis of 2-(E)-O-(4-Hydroxy-cinnamoyl)-ᴅ,ʟ-galactaric Acid, a Presumptive Photosensitive Factor from Glycine max". Zeitschrift für Naturforschung C 43, № 7-8 (1988): 519–28. http://dx.doi.org/10.1515/znc-1988-7-808.

Full text
Abstract:
The synthesis of 2-(E)-O-(4-hydroxy-cinnamoyl)-ᴅ,ʟ-galactaric acid (1a) is described. Starting with free galactaric acid (2) and 4-acetoxy-cinnamoyl-chloride (3), these compounds were esterified under regioselective conditions to racemic 2-(E)-O-(4-acetoxy-cinnamoyl)-galactaric acid (4). After deprotection of the p-coumaroyl moiety 1a was obtained as a photo-unstable product. Optical resolution of racemate l a on bovine serum albumin covalently bound to silica resulted in the isolation of the pure optical isomers. The (+)-dextrorotatory synthetic enantiomer l a proved to be identical with the
APA, Harvard, Vancouver, ISO, and other styles
4

Toma, Štefan, та Marta Sališová. "Acylation of ω-phenylalkanoylferrocenes by cinnamoyl and phenylpropiolyl chlorides". Collection of Czechoslovak Chemical Communications 52, № 6 (1987): 1520–26. http://dx.doi.org/10.1135/cccc19871520.

Full text
Abstract:
In Friedel-Crafts acylation of ω-phenylalkanoylferrocenes, the site of electrophilic attack depends on the reagent used. The acylation with cinnamoyl chloride yields preferentially the products of substitution of the unsubstituted cyclopentadienyl ring of ferrocene. The acylation with phenylpropionyl chloride affords the products of acylation of the benzene ring of the starting compound. The different behaviour of both acylating agents is discussed.
APA, Harvard, Vancouver, ISO, and other styles
5

Kawamura, Aki, Haijing Liu, Chika Takai, Takashi Takei, Hadi K. Razavi, and Masayoshi Fuji. "Surface modification of fumed silica by photo-dimerization reaction of cinnamyl alcohol and cinnamoyl chloride." Advanced Powder Technology 27, no. 2 (2016): 765–72. http://dx.doi.org/10.1016/j.apt.2016.03.003.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Lowe, Henry IC, Ngeh J. Toyang, Charah T. Watson, and Joseph Bryant. "Synthesis of Substituted 1,3-Diesters of Glycerol Using Wittig Chemistry." Natural Product Communications 9, no. 5 (2014): 1934578X1400900. http://dx.doi.org/10.1177/1934578x1400900526.

Full text
Abstract:
1,3-di-O-Cinnamoyl-glycerol is a natural compound isolated from a Jamaican medicinal plant commonly referred to as Ball moss (Tillandsia recurvata). The synthesis of this compound was achieved via a Wittig chemistry process. The synthetic approach started with acylation of a di-protected glycerol with cinnamoyl chloride, deprotection of the glycerol moiety, reaction of the primary alcohol with bromo acetylbromide followed by treatment with triphenyl phosphine to give the corresponding phosphonium bromide. The phosphonium bromide was then converted in situ to the Wittig reagent which is the bas
APA, Harvard, Vancouver, ISO, and other styles
7

Teponno, Rémy B., Sara R. Noumeur, and Marc Stadler. "Semisynthetic derivatives of massarilactone D with cytotoxic and nematicidal activities." Beilstein Journal of Organic Chemistry 21 (March 17, 2025): 607–15. https://doi.org/10.3762/bjoc.21.48.

Full text
Abstract:
Massarilactones constitute a rare class of polyketides produced mainly by endophytic fungi. Given that semisynthetic derivatives often exhibit biological activities greater than those of the substrates, seven previously unreported derivatives of massarilactone D, compounds 2–8, were synthetized by acylation with methacryloyl chloride, cinnamoyl chloride, 4-bromobenzoyl chloride, trans-2-methyl-2-butenoyl chloride, and crotonyl chloride. These compounds were evaluated for their cytotoxic activity against the murine fibroblasts L929, human cervix carcinoma KB-3-1, human lung carcinoma A549, huma
APA, Harvard, Vancouver, ISO, and other styles
8

Nechifor, Marioara. "Aromatic polyesters with photosensitive side chains: Synthesis, characterization and properties." Journal of the Serbian Chemical Society 81, no. 6 (2016): 673–85. http://dx.doi.org/10.2298/jsc160111026n.

Full text
Abstract:
New aromatic polyesters with photosensitive groups in their pendant chains were prepared from a diphenol carrying as substituent a cinnamoyl group extended with a flexible oxyethyleneoxy spacer and different aromatic dicarboxylic acids via direct polyesterification reaction in the presence of tosyl chloride/pyridine/dimethylformamide system as condensing agent. The resulting polyesters were characterized using Fourier-transform IR, proton and carbon nuclear magnetic resonance and ultraviolet spectroscopy, differential scanning calorimetry, thermogravimetric analysis, wide-angle X-ray diffracto
APA, Harvard, Vancouver, ISO, and other styles
9

Ma, Yuan, Zhen Zhang, and Yufen Zhao. "Microwave-Assisted One-Pot Synthesis of Dihydrocoumarins from Phenols and Cinnamoyl Chloride." Synlett 2008, no. 07 (2008): 1091–95. http://dx.doi.org/10.1055/s-2008-1042921.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

NEELAKUMARI, S., and G. RAVEENDRAN. "A Mechanistic Approach on the Solvolysis of Cinnamoyl Chloride in the Presence and Absence of Mercuric Chloride Catalyst." Oriental Journal Of Chemistry 29, no. 1 (2013): 341–46. http://dx.doi.org/10.13005/ojc/290155.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Cinnamoyl chloride"

1

Lee, Chia-Jui, та 李家睿. "Direct β-Acylation of 2-Arylidene-1,3-indandiones withAcyl Chlorides Catalyzed by OrganophosphanesPreparation of Furo[3,2-c]coumarins from 3-cinnamoyl-4-hydroxy-2H-chromen-2-ones and Acyl Chlorides: A Bu3P-Mediated C-Acylation/Cyclization SequenceSynthesis of Functionalized Furans via Chemoselective Reduction/Wittig reaction Using Catalytic Triethylamine and Phosphine". Thesis, 2016. http://ndltd.ncl.edu.tw/handle/58559388773676205184.

Full text
Abstract:
博士<br>國立臺灣師範大學<br>化學系<br>104<br>In part I, we have developed an organophosphane-catalyzed direct β-acylation of a series of conjugated systems bearing ketone, amide and ester functionalities using acyl chlorides as trapping reagents. A wide variety of highly functional ketone derivatives were generated efficiently under very mild conditions with high yields according to our protocol. Our adducts can even be utilized as important building blocks for the synthesis of functional tri/tetracyclic pyridazine derivatives. In part II, electrophilic addition of acyl chlorides to 3- cinnamoyl-4-hydroxy
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Cinnamoyl chloride"

1

Quraishi, M. A., and V. Bhardwaj. "Inhibition of Metallic Corrosion by Some 2-Cinnamyl Imidazoline Salts under Vapor Phase Conditions." In CORROSION 2003. NACE International, 2003. https://doi.org/10.5006/c2003-03365.

Full text
Abstract:
Abstract Four organic volatile corrosion inhibitors (VCIs) were synthesized using 2-cinnamyl imidazoline with various acids such as salicylic acid, maleic acid, nitrobenzoic acid and phthalic acid and evaluated as corrosion inhibitors of mild steel, brass and copper by weight loss method. Eschke test method, sodium chloride inoculation test method and sulfur dioxide (SO2) test method were also carried out to investigate the corrosion inhibiting effect of the compounds. All the investigated VCIs exhibited good inhibition efficiency (IE) for all the metals. Phthalate salt showed best result amon
APA, Harvard, Vancouver, ISO, and other styles
2

J., Otgontuul, Sevjidsuren G., and Altantsog P. "SOME RESULTS OF CINNAMOYL CHLORIDE (C9H7CLO) ORGANIC CRYSTAL." In НАНОМАТЕРИАЛЫ И ТЕХНОЛОГИИ. Buryat State University Publishing Department, 2016. http://dx.doi.org/10.18101/978-5-9793-0898-2-97-103.

Full text
APA, Harvard, Vancouver, ISO, and other styles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!