Relevant bibliographies by topics / Allene-Alkyne cross coupling

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  2. Dissertations / Theses

Academic literature on the topic 'Allene-Alkyne cross coupling'

Author: Grafiati
Published: 7 July 2024
Last updated: 31 July 2025

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Journal articles on the topic "Allene-Alkyne cross coupling"

1

Cabezas, Jorge A., and Natasha Ferllini. "Regiospecific Palladium-Catalyzed Cross-Coupling Reactions Using the Operational Equivalent of 1,3-Dilithiopropyne." Synthesis 52, no. 16 (2020): 2387–94. http://dx.doi.org/10.1055/s-0039-1690895.

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A regiospecific palladium-catalyzed cross-coupling reaction using the operational equivalent of the dianion 1,3-dilithiopropyne, with aromatic iodides is reported. This reaction gives high yields of 1-propyn-1-yl-benzenes and 2-(propyn-1-yl)thiophenes in the presence of catalytic amounts of palladium(0) or (II) and stoichiometric amounts of copper iodide. No terminal alkyne or allene isomers were detected. Reaction conditions were very mild and several functional groups were tolerated.
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2

Shimp, Heidi L., Alissa Hare, Martin McLaughlin, and Glenn C. Micalizio. "Allene–alkyne cross-coupling for stereoselective synthesis of substituted 1,4-dienes and cross-conjugated trienes." Tetrahedron 64, no. 16 (2008): 3437–45. http://dx.doi.org/10.1016/j.tet.2008.02.015.

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3

Shimp, Heidi L., and Glenn C. Micalizio. "An alkoxide-directed alkyne–allene cross-coupling for stereoselective synthesis of 1,4-dienes." Chemical Communications, no. 43 (2007): 4531. http://dx.doi.org/10.1039/b708256h.

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4

Zheng, Weixin, Yangfeng Wu, Fenfen Zheng, Linfeng Hu та Ya Hong. "Selective synthesis of α-methylenyl zirconacyclopentene via cross-coupling of alkyne and allene". Tetrahedron Letters 51, № 36 (2010): 4702–4. http://dx.doi.org/10.1016/j.tetlet.2010.06.134.

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5

Shimp, Heidi L., Alissa Hare, Martin McLaughlin, and Glenn C. Micalizio. "Reprint of “Allene–alkyne cross-coupling for stereoselective synthesis of substituted 1,4-dienes and cross-conjugated trienes”." Tetrahedron 64, no. 29 (2008): 6831–37. http://dx.doi.org/10.1016/j.tet.2008.03.086.

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6

Zheng, Weixin, Yangfeng Wu, Fenfen Zheng, Linfeng Hu та Ya Hong. "ChemInform Abstract: Selective Synthesis of α-Methylenyl Zirconacyclopentene via Cross-Coupling of Alkyne and Allene." ChemInform 41, № 47 (2010): no. http://dx.doi.org/10.1002/chin.201047067.

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7

Shimp, Heidi L., Alissa Hare, Martin McLaughlin, and Glenn C. Micalizio. "ChemInform Abstract: Allene-Alkyne Cross-Coupling for Stereoselective Synthesis of Substituted 1,4-Dienes and Cross-Conjugated Trienes." ChemInform 39, no. 40 (2008). http://dx.doi.org/10.1002/chin.200840057.

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8

Shimp, Heidi L., and Glenn C. Micalizio. "ChemInform Abstract: An Alkoxide-Directed Alkyne—Allene Cross-Coupling for Stereoselective Synthesis of 1,4-Dienes." ChemInform 39, no. 11 (2008). http://dx.doi.org/10.1002/chin.200811055.

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9

Shimp, Heidi L., Alissa Hare, Martin McLaughlin, and Glenn C. Micalizio. "ChemInform Abstract: Reprint of “Allene-Alkyne Cross-Coupling for Stereoselective Synthesis of Substituted 1,4-Dienes and Cross-Conjugated Trienes”." ChemInform 40, no. 6 (2009). http://dx.doi.org/10.1002/chin.200906053.

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Dissertations / Theses on the topic "Allene-Alkyne cross coupling"

1

Christin, Orane. "Synthèse totale de l’énacyloxine IIa, un antibiotique d’origine naturelle au mécanisme d’action original." Electronic Thesis or Diss., Université Paris Cité, 2023. http://www.theses.fr/2023UNIP5197.

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Abstract:
Isolée en 1982 par l'équipe de Watanabe à partir de la souche bactérienne Frateuria sp. W-315, l'énacyloxine IIa est un antibiotique polyénique présentant une forte activité contre les bactéries à Gram positif et à Gram négatif, ainsi qu'une activité plus faible contre les champignons. Ce polycétide se compose d'une chaîne linéaire de 23 carbones portant 6 centres stéréogènes, parmi lesquels un est chloré. Il comprend également un pentaène fragile doté d'un chlorure de vinyle, ainsi qu'un cyclohexane possédant 3 centres stéréogènes. L'énacyloxine IIa est une molécule dont la complexité laisse
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