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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 31, 2001 - Issue 15
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Original Articles

A MILD AND FEASIBLE DEPROTECTION OF ALCOHOL TETRAHYDROPYRANYL OR METHOXYMETHYL ETHERS CATALYZED BY Sc(OTf)3

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Pages 2305-2311 | Received 04 Sep 2000, Published online: 09 Nov 2006

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Read on this site (2)

F. Shirini, K. Marjani & H. Taherpour Nahzomi. (2007) Silica Triflate as a New, Mild and Efficient Catalyst for Tetrahydropyranylation of Alcohols and Deprotection of Tetrahydropyranyl Ethers. Phosphorus, Sulfur, and Silicon and the Related Elements 182:9, pages 2235-2240.
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William H. Miles, Daniel A. Ruddy, Samira Tinorgah & Rebecca L. Geisler. (2004) Acylative Dimerization of Tetrahydrofuran Catalyzed by Rare‐Earth Triflates. Synthetic Communications 34:10, pages 1871-1880.
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Articles from other publishers (15)

Dayong Sang, Huaxin Yue, Zhengdong Zhao, Pengtao Yang & Juan Tian. (2020) Anchimerically Assisted Selective Cleavage of Acid-Labile Aryl Alkyl Ethers by Aluminum Triiodide and N , N -Dimethylformamide Dimethyl Acetal . The Journal of Organic Chemistry 85:10, pages 6429-6440.
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Thanh C. Ho, Naoyuki Shimada, Marcus A. Tius, Spyros P. Nikas, Wen Zhang & Alexandros Makriyannis. (2017) C 1′-Azacycloalkyl Hexahydrocannabinols . The Journal of Organic Chemistry 82:15, pages 7839-7849.
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Marjolein van der Kaaden, Eefjan Breukink & Roland J Pieters. (2012) Synthesis and antifungal properties of papulacandin derivatives. Beilstein Journal of Organic Chemistry 8, pages 732-737.
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Iraj Mohammadpoor-Baltork, Majid Moghadam, Shahram Tangestaninejad, Valiollah Mirkhani, Ahmad Reza Khosropour & Arsalan Mirjafari. (2010) Microwave-assisted rapid and efficient deprotection and direct esterification and silylation of MOM and EOM ethers catalyzed by [Hmim][HSO4] as a Brønsted acidic ionic liquid. Monatshefte für Chemie - Chemical Monthly 141:10, pages 1083-1088.
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Jesse B. Davis, J. Daniel Bailey & Jason K. Sello. (2009) Biomimetic Synthesis of a New Class of Bacterial Signaling Molecules. Organic Letters 11:14, pages 2984-2987.
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Zhi-Bin Zhen, Jian Gao & Yikang Wu. (2008) A Chiron Approach to the Total Synthesis of (+)-Aculeatin D. The Journal of Organic Chemistry 73:18, pages 7310-7316.
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Hafida Gaspard‐Iloughmane & Christophe Le Roux. (2004) Bismuth( III ) Triflate in Organic Synthesis . European Journal of Organic Chemistry 2004:12, pages 2517-2532.
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S. Venkat Reddy, R. Jagadeeshwar Rao, U. Sampath Kumar & J. Madhusudana Rao. (2003) Highly Efficient and Convenient Deprotection of Methoxymethyl Ethers and Esters Using Bismuth Triflate in an Aqueous Medium. Chemistry Letters 32:11, pages 1038-1039.
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Jacqueline R. Stephens, Phillip L. Butler, Curtis H. Clow, Matthew C. Oswald, Russell C. Smith & Ram S. Mohan. (2003) Bismuth Triflate: An Efficient Catalyst for the Formation and Deprotection of Tetrahydropyranyl Ethers. European Journal of Organic Chemistry 2003:19, pages 3827-3831.
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Michael B. Smith. 2003. Compendium of Organic Synthetic Methods. Compendium of Organic Synthetic Methods 18 89 .
Gustavo P. Romanelli, Graciela Baronetti, Horacio J. Thomas & Juan C. Autino. (2002) Efficient method for tetrahydropyranylation/depyranylation of phenols and alcohols using a solid acid catalyst with Wells–Dawson structure. Tetrahedron Letters 43:42, pages 7589-7591.
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Shū Kobayashi, Masaharu Sugiura, Hidetoshi Kitagawa & William W.-L. Lam. (2002) Rare-Earth Metal Triflates in Organic Synthesis. Chemical Reviews 102:6, pages 2227-2302.
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Tsutomu Watahiki, Hisashi Kikumoto, Masaya Matsuzaki, Takeshi Suzuki & Takeshi Oriyama. (2002) A Novel and Efficient Method for the Synthesis of Tetrahydropyranyl Ethers Catalyzed by Sc(OTf) 3 . Bulletin of the Chemical Society of Japan 75:2, pages 367-368.
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Alan C. Spivey & David Leese. (2002) 2  Synthetic methods : Part (iii) Protecting groups. Annu. Rep. Prog. Chem., Sect. B: Org. Chem. 98, pages 41-60.
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Takeshi Oriyama, Tsutomu Watahiki, Yoshinobu Kobayashi, Hiroyuki Hirano & Takeshi Suzuki. (2010) ChemInform Abstract: A Mild and Feasible Deprotection of Alcohol Tetrahydropyranyl or Methoxymethyl Ethers Catalyzed by Sc(OTf) 3 . . ChemInform 32:48.
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