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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 12, 1982 - Issue 9
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Original Articles

A Mild and Versatile Method for Carboxy Group Activation and Esterification

S. Chandrasekaran Research School of Chemistry, Australian National University, P. O. Box 4, Canberra, A. C. T. 2600, Australia
&
John V. Turner Research School of Chemistry, Australian National University, P. O. Box 4, Canberra, A. C. T. 2600, Australia
Pages 727-731 | Published online: 05 Dec 2006

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Peter A. Jacobi & E. Hampton$suffix/text()$suffix/text(). (2003) On the Methylation of Carboxyl Groups with Methanesulfonyl Chloride in Pyridine. Synthetic Communications 33:15, pages 2575-2579.
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Tai-Bao Wei & You-Ming Zhang. (1999) Facile and Effective Synthesis of N-Aryl-2-Furancarboxamides Derivatives Under the Condition of Phase Transfer Catalysis. Synthetic Communications 29:17, pages 2943-2947.
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Articles from other publishers (28)

Debasis Sahoo, Sohini Sarkar & Samaresh Jana. (2019) A simple synthesis of ketone from carboxylic acid using tosyl chloride as an activator. Tetrahedron Letters 60:39, pages 151084.
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Junzo Otera & Joji Nishikido. 2009. Esterification. Esterification 325 361 .
Zhaohua Yan, Weisheng Tian, Fanrong Zeng & Yanfeng Dai. (2009) 5H-3-oxa-Octafluoropentanesulfonyl fluoride: a novel and efficient condensing agent for esterification, amidation and anhydridization. Tetrahedron Letters 50:23, pages 2727-2729.
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Denise Andersen, Thomas Storz, Pingli Liu, Xin Wang, Leping Li, Pingchen Fan, Xiaoqi Chen, Alan Allgeier, Alain Burgos, Jason Tedrow, Jean Baum, Ying Chen, Rich Crockett, Liang Huang, Rashid Syed, Robert D. Larsen & Mike Martinelli. (2007) Stereoselective Synthesis of a MCHr1 Antagonist. The Journal of Organic Chemistry 72:25, pages 9648-9655.
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Ju-Eun Won, Ho-Kyun Kim, Jeum-Jong Kim, Heong-Seup Yim, Min-Jung Kim, Seung-Beom Kang, Hyun-A. Chung, Sang-Gyeong Lee & Yong-Jin Yoon. (2007) Effective esterification of carboxylic acids using (6-oxo-6H-pyridazin-1-yl)phosphoric acid diethyl ester as novel coupling agents. Tetrahedron 63:51, pages 12720-12730.
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C.K.-F. Chiu, M.A. Berliner & Z.B. Li. 2005. Comprehensive Organic Functional Group Transformations II. Comprehensive Organic Functional Group Transformations II 595 658 .
Jacqueline C. S. Woo, Erik Fenster & Gregory R. Dake. (2004) A Convenient Method for the Conversion of Hindered Carboxylic Acids to N -Methoxy- N -methyl (Weinreb) Amides . The Journal of Organic Chemistry 69:25, pages 8984-8986.
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. (2004) An Efficient and Convenient Esterification of Carboxylic Acids Using 4,5-Dichloro-2-[(4-nitrophenyl)sulfonyl]pyridazin-3(2H)-one. Bulletin of the Korean Chemical Society 25:4, pages 501-505.
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John C. Gilbert, Jiandong Yin, Fatima H. Fakhreddine & Matthew L. Karpinski. (2004) Facial selectivity of the Ireland?Claisen rearrangement of allylic esters of 2-methyl and 2-methoxycyclopentanecarboxylic acids. Tetrahedron 60:1, pages 51-60.
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Kazunori Wakasugi, Atsushi Nakamura, Akira Iida, Yoshinori Nishii, Nobuji Nakatani, Shoji Fukushima & Yoo Tanabe. (2003) Novel and efficient method for esterification, amidation between carboxylic acids and equimolar amounts of alcohols, and amines utilizing Me2NSO2Cl and N,N-dimethylamines; its application to the synthesis of coumaperine, a natural chemopreventive dieneamide. Tetrahedron 59:28, pages 5337-5345.
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N Zander & R Frank. (2001) Polystyrylsulfonyl chloride resin: an efficient solid-supported condensation reagent for the solution phase synthesis of esters. Tetrahedron Letters 42:44, pages 7783-7785.
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K. C. Nicolaou, Phil S. Baran, Yong-Li Zhong, Ha-Soon Choi, Kin Chiu Fong, Yun He & Won Hyung Yoon. (1999) New Synthetic Technology for the Synthesis of Hindered α-Diazoketones via Acyl Mesylates. Organic Letters 1:6, pages 883-886.
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Khanitha Pudhom & Tirayut Vilaivan. (1999) Synthesis of aryl esters of protected amino acids from aryl sulfonates. Tetrahedron Letters 40:32, pages 5939-5942.
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Shoei-Sheng Lee, Wen-Chuan Chen, Chih-Fen Huang & Yeu Su. (1998) Preparation and Cytotoxic Effect of Ceanothic Acid Derivatives. Journal of Natural Products 61:11, pages 1343-1347.
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Xun Li & David P. Rotella. (1994) Synthesis and structural analysis of stereospecific 3,4,5-trisubstituted γ-butyrolactone phospholipids. Lipids 29:3, pages 211-224.
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Ludovic Jullien, Josette Canceill, Liliane Lacombe & Jean-Marie Lehn. (1994) Analysis of the conformational behaviour of perfunctionalized β-cyclodextrins. Part 1. Evidence for insertion of one of the rim substituents into the cyclodextrin cavity in organic solvents. J. Chem. Soc., Perkin Trans. 2:5, pages 989-1002.
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Mikhail S. Ermolenko, Alain Olesker & Gabor Lukacs. (1994) Stereoselective synthesis of the tetrasubstituted cyclohexane core of a monocyclic mevinic acid analogue. Tetrahedron Letters 35:5, pages 711-714.
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John C. Gilbert & Robert D. Selliah. (1994) Enantioselective synthesis of an ent-trichothecene. Tetrahedron 50:6, pages 1651-1664.
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David D. Wirth. (1993) Carboxylic sulfonic mixed anhydrides: General utility and application to the synthesis of ceftazidime. Tetrahedron 49:8, pages 1535-1540.
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KF Cheng, TT Wong, KP Chan & YC Kong. (1992) Structure-function relationship of Yuehchukene II. The effect of C-6 indole rotation on anti-implantation activity. European Journal of Medicinal Chemistry 27:2, pages 121-130.
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Piétrick Hudhomme, Loic Toupet & Guy Duguay. (1990) Resolution of multifunctional carbon compounds derivated from N-protected 2-cyano glycinates. Tetrahedron: Asymmetry 1:9, pages 611-620.
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C. G. Kruse, J. J. Troost, P. Cohen‐Fernandes, H. van der Linden & J. D. van Loon. (2010) Single‐step conversion of aliphatic, aromatic and heteroaromatic primary amines into piperazine‐2,6‐diones. Recueil des Travaux Chimiques des Pays-Bas 107:4, pages 303-309.
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Peter Jütten, Jürgen Dornhagen & Hans-Dieter Scharf. (1987) Syntheses of the methyl glycosides of curacin, a-b fragment found in avilamycin-a and -c, curamycin-a, flambamycin and everninomicin-2, and of its artificial regioisomer isocuracin. Tetrahedron 43:18, pages 4133-4140.
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C.M. Lok, A.P.J. Mank & J.P. Ward. (1985) Synthesis of glycidol esters and mono/di-acylglycerols from glycidol. Chemistry and Physics of Lipids 36:4, pages 329-334.
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. 1984. Compendium of Organic Synthetic Methods. Compendium of Organic Synthetic Methods 224 255 .
S. CHANDRASEKARAN & J. V. TURNER. (2016) ChemInform Abstract: A MILD AND VERSATILE METHOD FOR CARBOXY GROUP ACTIVATION AND ESTERIFICATION. Chemischer Informationsdienst 14:14.
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William G Dauben, Richard A Bunce, John M Gerdes, Kevin E Henegar, Allan F CunninghamJr.Jr. & Thomas B Ottoboni. (1983) Organic reactions at high pressure. A mild method for the placement of protecting groups on hindered and sensitive alcohols. Tetrahedron Letters 24:51, pages 5709-5712.
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Sunggak Kim, Youn Chul Kim & Jae In Lee. (1983) A new convenient method for the esterification of carboxylic acids. Tetrahedron Letters 24:32, pages 3365-3368.
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