Log in

Relevant bibliographies by topics / Dimethyl acetylenedicarboxylate

Contents

Journal articles
Dissertations / Theses
Book chapters
Conference papers

Academic literature on the topic 'Dimethyl acetylenedicarboxylate'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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 'Dimethyl acetylenedicarboxylate.'

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 "Dimethyl acetylenedicarboxylate"

1

Han, Ying, Chao-Guo Yan, Chang-Zhou Liu, Yuan-Yuan Zhang, and Jing Sun. "Nucleophilic Phosphine-Promoted Domino Reaction of Dialkyl Acetylenedicarboxylates and 3-Arylamino-1-methyl-1H-pyrrole-2,5-diones." Synthesis 50, no. 18 (2018): 3715–22. http://dx.doi.org/10.1055/s-0037-1610438.

Full text

Abstract:

The three-component reaction of triphenylphosphine, dimethyl acetylenedicarboxylate and 3-arylamino-1-methyl-1H-pyrrole-2,5-diones in CH2Cl2 at room temperature resulted in functionalized 3-(triphenyl-λ5-phosphanylidene)succinates in nearly quantitative yields. However, tri(n-butyl)phosphine promoted reaction of dialkyl acetylenedicarboxylates and 3-arylamino-1-methyl-1H-pyrrole-2,5-diones in CH2Cl2 afforded functionalized pyrrolo[3,4-b]pyridine-4-carboxylates in satisfactory yields.

APA, Harvard, Vancouver, ISO, and other styles

2

Anary-Abbasinejad, Mohammad, Hossein Anaraki-Ardakani, Alimohammad Dehghan, Alireza Hassanabadi, and Mohammad Reza Seyedmir. "A One-Pot Synthesis of Functionalised 3-pyrolin-2-ones by a four-component reaction between Triphenylphosphine, Primary Amines, Dimethyl Acetylenedicarboxylate and Ethyl Chlorooxoacetate." Journal of Chemical Research 2007, no. 10 (2007): 574–76. http://dx.doi.org/10.3184/030823407x255542.

Full text

Abstract:

Reaction between triphenylphosphine, dimethy acetylenedicarboxylate and amines produces phosphorus ylids which undergo a smooth reaction with ethyl chlorooxoacetate and triethylamine to produce dimethyl N-aryl-(or alkyl)-4-ethoxy-5-oxo-2,5-dihydro-1 H-pyrole-2,3-dicarboxylates in high yields.

APA, Harvard, Vancouver, ISO, and other styles

3

Anary-Abbasinejad, Mohammad, Mohammad H. Mosslemin, Alireza Hassanabadi, and Alimohammad Dehghan. "Synthesis of Functionalised Phosphonates or Phosphoranes by Reaction between Trialkyl Phosphites or Triphenylphosphine, Dimethyl Acetylenedicarboxylate and Aldehyde Ethyl Carbazones." Journal of Chemical Research 2009, no. 5 (2009): 329–32. http://dx.doi.org/10.3184/030823409x447709.

Full text

Abstract:

Protonation of the reactive intermediate produced from the reaction between trialkyl phosphites and dimethyl acetylenedicarboxylate by ethyl carbazones of aromatic aldehydes following by conjugate addition of the anion of ethyl carbazone on the phosphonium salt intermediate leads to functionalised phosphonates in good yields. Triphenylphosphine also reacted with dimethyl acetylenedicarboxylate and ethyl carbazones to produce functionalised phosphoranes in good yields.

APA, Harvard, Vancouver, ISO, and other styles

4

Lin, Qinghong, Djamal Djaidi, Roger Bishop, Donald C. Craig, and Marcia L. Scudder. "Ritter Reactions. XIII Reactivity of Methyl Schiff Bases with Dimethyl Acetylenedicarboxylate and Mercaptoacetic Acid." Australian Journal of Chemistry 51, no. 9 (1998): 799. http://dx.doi.org/10.1071/c98025.

Full text

Abstract:

Reactions of several methyl imines with dimethyl acetylenedicarboxylate and with mercaptoacetic acid have been studied to investigate further the capricious behaviour of this functionality. The 1 : 1 adduct of imine (1) and dimethyl acetylenedicarboxylate is confirmed as the pyrroloisoquinoline structure (7) by X-ray methods [C17H17NO5, P -1, a 9·037(2), b 9·276(2), c 10·033(2) Å, α 81·99(1), β 81·28(1), γ 64·9(2)°, Z 2, R 0·044]. New products from (2) and dimethyl acetylenedicarboxylate, the 1 : 1 adduct (10) which is readily converted into the known product (9), and the 1 : 2 adduct (12), ar

APA, Harvard, Vancouver, ISO, and other styles

5

Dmowski, Wojciech, and Albert Biernacki. "Electrochemical trifluoromethylation of dimethyl acetylenedicarboxylate." Journal of Fluorine Chemistry 78, no. 2 (1996): 193–94. http://dx.doi.org/10.1016/0022-1139(96)03443-4.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Vo, Timothy H., Rafał Korlacki, and Alexander Sinitskii. "Cis–trans isomerization of dimethyl 2,3-dibromofumarate." RSC Advances 12, no. 50 (2022): 32471–74. http://dx.doi.org/10.1039/d2ra05996g.

Full text

Abstract:

The bromination of dimethyl acetylenedicarboxylate initially results in mostly trans dimethyl 2,3-dibromofumarate, which then converts into the more stable cis isomer. The trans-to-cis conversion is spontaneous and greatly accelerated by light.

APA, Harvard, Vancouver, ISO, and other styles

7

Schwan, Adrian L., та John Warkentin. "Reactions of 4-tert-butyl-5-methylene-3,3-dimethyl-Δ1-1,2,4-triazoline with dimethyl acetylenedicarboxylate". Canadian Journal of Chemistry 65, № 6 (1987): 1200–1204. http://dx.doi.org/10.1139/v87-201.

Full text

Abstract:

4-tert-Butyl-5-methylene-3,3-dimethyl-Δ1-1,2,4-triazoline (1) reacts rapidly with dimethyl acetylenedicarboxylate (2) to afford dienamines 3 and 4 from Michael addition and enamine 5 by extensive skeletal rearrangement. Assignments of their structures and probable mechanisms of their formation are discussed.

APA, Harvard, Vancouver, ISO, and other styles

8

Lim, Suk Hyun, Hannara Jang, and Dae Won Cho. "Fullerene C60 promoted photochemical hydroamination reactions of an electron deficient alkyne with trimethylsilyl group containing tertiary N-alkylbenzylamines." RSC Advances 11, no. 11 (2021): 5914–22. http://dx.doi.org/10.1039/d1ra00166c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Yap, Jeanette See Leng, Bin Bin Li, Jonathan Wong, Yongxin Li, Sumod A. Pullarkat, and Pak-Hing Leung. "Development of a novel chiral palladacycle and its application in asymmetric hydrophosphination reaction." Dalton Trans. 43, no. 15 (2014): 5777–84. http://dx.doi.org/10.1039/c4dt00062e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Matsumoto, Kiyoshi, Yukio Ikemi, Motoo Shiro, Takane Uchida, and James William Lown. "Reactions of 5-cyano-1,4-diphenylpyridazino[4,5-a]indolizines with dimethyl acetylenedicarboxylate: regioselective formation of 1:2 Michael type adducts." Canadian Journal of Chemistry 71, no. 4 (1993): 529–33. http://dx.doi.org/10.1139/v93-075.

Full text

Abstract:

Reactions of 5-cyano-1,4-diphenylpyridazino[4,5-a]indolizines with dimethyl acetylenedicarboxylate afforded the 1:2 adducts regioselectively and, unexpectedly, in a Michael fashion rather than in a 1,3-dipolar manner. The structure of the products was established by X-ray crystallography. Regiospecific formation of the observed product 3 can be explained by the higher nucleophilicity of the nitrogen at the 2 position than at the 3 position of the 5-cyano-1,4-diphenylpyridazino[4,5-a]indolizine 1 owing to the contribution of a resonance structure 5 to the hybrid. This favors two successive Mich

APA, Harvard, Vancouver, ISO, and other styles

More sources

Dissertations / Theses on the topic "Dimethyl acetylenedicarboxylate"

1

Iqbal, Inam [Verfasser]. "Synthesis of functionalized 2-(arylthio)benzoates by cyclization of 3-arylthio-1-silyloxy-1,3-butadienes with 3-silyloxy-2-en-1-ones, 3-alkoxy-2-en-1-ones, 1,1-diacylcyclopropanes, and dimethyl acetylenedicarboxylate / vorgelegt von Inam Iqbal." 2009. http://d-nb.info/995969477/34.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Dimethyl acetylenedicarboxylate"

1

von Angerer, S. "With Dimethyl Acetylenedicarboxylate." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01024.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Stanovnik, B., and J. Svete. "From Arylhydrazones and Dimethyl Acetylenedicarboxylate." In Five-Membered Hetarenes with Two Nitrogen or Phosphorus Atoms. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-012-00093.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Murphy, P. J. "From Diphenyl Diselenide and Dimethyl Acetylenedicarboxylate." In Fused Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-00364.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Aitken, R. A. "Cycloaddition of Phospholes with Dimethyl Acetylenedicarboxylate." In Fused Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-01142.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Abou-Hadeed, K., and H. J. Hansen. "Reaction of Substituted Tropone Dimethyl Ketals with Dimethyl Acetylenedicarboxylate." In Monocyclic Arenes, Quasiarenes, and Annulenes. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-045-01162.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Aitken, R. A. "10.20 Phosphorus Analogues of Indolizines." In Knowledge Updates 2022/2. Georg Thieme Verlag KG, 2022. http://dx.doi.org/10.1055/sos-sd-110-02196.

Full text

Abstract:

AbstractThis chapter is a complete revision and update of the earlier Science of Synthesis contribution from 2000 describing methods for the synthesis of phosphorus analogues of indolizines. The previous route to this rare ring system, reaction of a phosphole with dimethyl acetylenedicarboxylate, has now been joined by a metathesis-based method leading to the parent dibenzophosphindolizine and its chalcogen derivatives.

APA, Harvard, Vancouver, ISO, and other styles

7

Hou, X. L., X. S. Peng, K. S. Yeung, and H. N. C. Wong. "From Dimethyl Acetylenedicarboxylate, Aldehydes, and Thiazolium Salts." In Fully Unsaturated Small-Ring Heterocycles and Monocyclic Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-109-00072.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Tominaga, Y. "Reaction of Cyclopenta[]quinolizine with Dimethyl Acetylenedicarboxylate." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01706.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Tominaga, Y. "Cycloaddition of Imino Compounds with Dimethyl Acetylenedicarboxylate." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01728.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Tominaga, Y. "Using Diels–Alder Reaction of Dimethyl Acetylenedicarboxylate." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01730.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Dimethyl acetylenedicarboxylate"

1

Cabrera, José, Mateo Alajarín, and Aurelia Pastor. "A Chemodivergent Issue in the Reactions of 4-alkenylthiazoles with Dimethyl Acetylenedicarboxylate." In The 9th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01476.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Diaconu, Dumitrela, Violeta Mangalagiu, Dorina Amariucai-Mantu, Vasilichia Antoci, Ramona Danac, and Ionel Mangalagiu. "1,3-dipolar cycloaddition reactions of benzimidazolium-ylides to an activated symmetric alkyne." In Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab27.

Full text

Abstract:

The cycloaddition reactions represent an important way to obtain cyclic structures and take place between two or more reactants containing double or triple bonds in the molecule. After Huisgen, the addition of 1,3-dipole to a dipolarophile, takes place through a concerted mechanism, when two  bonds are formed. [1,2] The purpose of this research is to study the Huisgen [3+2] dipolar cycloaddition reactions carried out in a conventional way (stirring at room temperature) and non-conventional way (ultrasonic irradiation), between benzimidazolium-ylides and an activated symmetric substituted alky

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!