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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 4, 1974 - Issue 4
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Original Articles

Synthesis of Acetylenic Carboxylic Acids

N. Gilman Chemical Research Department, Hoffmann-La Roche Inc., Nutley, New Jersey, 07110
&
B. Holland Chemical Research Department, Hoffmann-La Roche Inc., Nutley, New Jersey, 07110
Pages 199-202 | Received 12 Apr 1974, Published online: 06 Dec 2006

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Warongrit Sukma, Cheerapa Boonyakong, Thitiphan Chaiphet & Supakarn Chamni. (2024) A simple and rapid colorimetric detection of methanol, ethanol, and isopropanol and its application toward alcohol-based hand sanitizer quality control. Green Chemistry Letters and Reviews 17:1.
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W.J. Dejarlais & E.A. Emken. (1980) A Convenient Synthesis of ω-Acetylenic Acids. Synthetic Communications 10:9, pages 653-660.
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Articles from other publishers (18)

Rodney A. Fernandes, Dnyaneshwar A. Gorve & Ramdas S. Pathare. (2020) Emergence of 2,3,5-trisubstituted tetrahydrofuran natural products and their synthesis. Organic & Biomolecular Chemistry 18:36, pages 7002-7025.
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Dong Jin Yoo, Eun Young Kim, Michael Oelgemöller & Sang Chul Shim. (2004) Synthesis of cycloalkynes via photochemical decarboxylation of ω-phthalimidoalkynoates. Photochemical & Photobiological Sciences 3:3, pages 311-316.
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Sang Chul Shim, Dong Jin Yoo, Eun Young Kim & Michael Oelgem?ller. (2001) Synthesis of a Macroheterocyclic Compound through Photodecarboxylation of Potassium ?-Phthalimidoalkynoate. HETEROCYCLES 54:2, pages 1049.
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. 1995. Comprehensive Organic Functional Group Transformations. Comprehensive Organic Functional Group Transformations 1147 1316 .
Mark Furber. 1995. Comprehensive Organic Functional Group Transformations. Comprehensive Organic Functional Group Transformations 997 1085 .
J. George Pomonis & Heldur Hakk. (1990) Synthesis of ω9‐tetracosynoic and ω9‐octacosynoic acids as entries into tritiated metabolic precursors of cis ‐9‐tricosene and cis ‐9‐heptacosene in the housefly . Lipids 25:12, pages 821-826.
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J. Cossy & J.P. Pete. (1986) A one step synthesis of ?-hydroxyacetylenic carboxylic acids. Tetrahedron Letters 27:5, pages 573-574.
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M. Van De Ven, H. Van Langen, W. Verwer & Y.K. Levine. (1984) Raman spectra and conformations of n-hexadecynoic fatty acids and their potassium salts. Chemistry and Physics of Lipids 34:2, pages 185-200.
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W. J. Dejarlais, E. A. Emken & W. R. Miller. (2006) Syntheses of some di‐, tetra‐, and hexadeuterio‐octadecenoates. Journal of Labelled Compounds and Radiopharmaceuticals 19:10, pages 1135-1144.
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Joel Myerson, William F. Haddon & Edwin L. Soderstrom. (1982) Sec-butyl (Z)-7-tetradecenoate. A novel sex pheromone component from the western grapeleaf skeletonizer, harrsina brillians.. Tetrahedron Letters 23:27, pages 2757-2760.
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Henry Rakoff. (1982) Preparation of fatty acids and esters containing deuterium. Progress in Lipid Research 21:3, pages 225-254.
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Wolfgang Seidel & Hans J. Schäfer. (2006) Kolbe‐Synthese ungesättigter Pheromone durch Coelektrolyse mit 5‐Alkinsäuren. Chemische Berichte 113:12, pages 3898-3903.
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George Just, Corinne Luthe & Hunseung Oh. (1980) Oxidation products of arachidonic acid I. The synthesis of methyl 8R, 11R, 15-trihydroxy-9S, 12-oxyeicosa-5Z, 13E-dienoate (19). Tetrahedron Letters 21:11, pages 1001-1004.
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Andrew B Holmes & Graham E Jones. (1980) Synthesis of 4-alkyl-1-trimethylsilylbuta-1,3-diynes. Tetrahedron Letters 21:32, pages 3111-3112.
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Larry D. Lawson & Fred A. Kummerow. (1979) ?-Oxidation of the coenzyme a esters of elaidic, oleic, and stearic acids and their full-cycle intermediates by rat heart mitochondria. Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism 573:2, pages 245-254.
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John F.W. Keana & Lawrence E. La Fleur. (1979) Saturated and unsaturated lipid spin labels with terminally located nitroxide groups. Chemistry and Physics of Lipids 23:3, pages 253-265.
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Clive A. Henrick. (1977) The synthesis of insect sex phermones. Tetrahedron 33:15, pages 1845-1889.
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N. GILMAN & B. HOLLAND. (2016) ChemInform Abstract: SYNTHESIS OF ACETYLENIC CARBOXYLIC ACIDS. Chemischer Informationsdienst 5:51.
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