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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 15, 1985 - Issue 11
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Original Articles

Allylic Alcohols Via the Chemoselective Reduction of Enone Systems with Sodium Borohydride in Methanolic Tetrahydrofuran

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Pages 985-990 | Published online: 19 Dec 2006

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Ricardo Tapia, JaimeA. Valderrama & Claudio Saitz. (1994) A Simple Synthesis of Ethyl 5-(1,4-Cyclohexadiene-3,6-dione-1-yl)-3,5-dihydroxy Pentanoate. Synthetic Communications 24:11, pages 1625-1630.
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Claudio Saitz B.JaimeA. Valderrama & Ricardo Tapia. (1990) Studies on Quinones. XX. synthesis of 2-acetonylpyranonaphthoqoinones. Synthetic Communications 20:20, pages 3103-3114.
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R. Allen Rhodes & DavidW. Boykin. (1988) The Selective Reduction of α,β-Unstaurated Nitriles with Sodium Borohydride in Methanolic Pyridine. Synthetic Communications 18:7, pages 681-687.
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Articles from other publishers (31)

Todd E. Markham, Andrew C. Kotze, Peter J. Duggan & Martin R. Johnston. (2021) Reduction Chemistry of Natural Pyrethrins and Preliminary Insecticidal Activity of Reduced Pyrethrins. Australian Journal of Chemistry 74:4, pages 268.
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Louis F. Fieser, Mary Fieser & Tse‐Lok HoTse‐Lok Ho, Mary Fieser, Louis Fieser, Rick Danheiser, William Roush & Janice Smith. 2006. Fieser and Fieser's Reagents for Organic Synthesis. Fieser and Fieser's Reagents for Organic Synthesis.
Louis F. Fieser, Mary Fieser & Tse‐Lok HoTse‐Lok Ho, Mary Fieser, Louis Fieser, Rick Danheiser, William Roush & Janice Smith. 2006. Fieser and Fieser's Reagents for Organic Synthesis. Fieser and Fieser's Reagents for Organic Synthesis.
Ulrich Wietelmann, Michael Felderhoff & Peter Rittmeyer. 2000. Ullmann's Encyclopedia of Industrial Chemistry. Ullmann's Encyclopedia of Industrial Chemistry 1 39 .
Naveen, Srinivasarao Arulananda Babu, Nayyar Ahmad Aslam, Akshey Sandhu, Dharmendra Kumar Singh & Ameet Rana. (2015) Direct azidation of allylic/benzylic alcohols and ethers followed by the click reaction: one-pot synthesis of 1,2,3-triazoles and 1,2,3-triazole moiety embedded macrocycles. Tetrahedron 71:38, pages 7026-7045.
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Luca Banfi, Enrica Narisano, Renata Riva, Nikola Stiasni, Martin Hiersemann, Tohru Yamada & Tatsuyuki Tsubo. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis 1 13 .
Davood Setamdideh, Zahra Karimi & Avat Alipouramjad. (2013) NaBH 4 /DOWEX(R)50WX4: A Convenient Reducing System for Fast and Efficient Reduction of Carbonyl Compounds to Their Corresponding Alcohols . Journal of the Chinese Chemical Society 60:6, pages 590-596.
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Louis F. Fieser, Mary Fieser & Tse‐Lok HoTse‐Lok Ho, Mary Fieser, Louis Fieser, Rick Danheiser, William Roush & Janice Smith. 2006. Fieser and Fieser's Reagents for Organic Synthesis. Fieser and Fieser's Reagents for Organic Synthesis 455 456 .
Louis F. Fieser, Mary Fieser & Tse‐Lok HoTse‐Lok Ho, Mary Fieser, Louis Fieser, Rick Danheiser, William Roush & Janice Smith. 2006. Fieser and Fieser's Reagents for Organic Synthesis. Fieser and Fieser's Reagents for Organic Synthesis 526 526 .
Akio Tanaka, Hideho Okamoto & Malcolm Bersohn. (2010) Construction of Functional Group Reactivity Database under Various Reaction Conditions Automatically Extracted from Reaction Database in a Synthesis Design System. Journal of Chemical Information and Modeling 50:3, pages 327-338.
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Ayla M.C. Bizerra, Gonzalo de Gonzalo, Iván Lavandera, Vicente Gotor-Fernández, Marcos Carlos de Mattos, Maria da Conceicão F. de Oliveira, Telma L.G. Lemos & Vicente Gotor. (2010) Reduction processes biocatalyzed by Vigna unguiculata. Tetrahedron: Asymmetry 21:5, pages 566-570.
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Louis F. Fieser, Mary Fieser & Tse‐Lok HoTse‐Lok Ho, Mary Fieser, Louis Fieser, Rick Danheiser, William Roush & Janice Smith. 2006. Fieser and Fieser's Reagents for Organic Synthesis. Fieser and Fieser's Reagents for Organic Synthesis 000 000 .
Louis F. Fieser, Mary Fieser & Tse‐Lok HoTse‐Lok Ho, Mary Fieser, Louis Fieser, Rick Danheiser, William Roush & Janice Smith. 2006. Fieser and Fieser's Reagents for Organic Synthesis. Fieser and Fieser's Reagents for Organic Synthesis 000 000 .
Luca Banfi, Enrica Narisano, Renata Riva, Nikola Stiasni & Martin Hiersemann. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis.
Marilena A. Giarrusso, Luke T. Higham, Ulf P. Kreher, Ram S. Mohan, Anthony E. Rosamilia, Janet L. Scott & Christopher R. Strauss. (2008) Platform technology for dienone and phenol–formaldehyde architectures. Green Chemistry 10:8, pages 842.
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Yu Yuan, Zhuangzhi Shi, Xuan Feng & Xiangnong Liu. (2007) Solvent‐free reactions of alcohols with β‐dicarbonyl compounds catalyzed by iron(III) chloride. Applied Organometallic Chemistry 21:11, pages 958-964.
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Louis F. Fieser, Mary Fieser & Tse‐Lok HoTse‐Lok Ho, Mary Fieser, Louis Fieser, Rick Danheiser, William Roush & Janice Smith. 2006. Fieser and Fieser's Reagents for Organic Synthesis. Fieser and Fieser's Reagents for Organic Synthesis.
Behzad Zeynizadeh & Davood Setamdideh. (2005) Water as a Green Solvent for Fast and Efficient Reduction of Carbonyl Compounds with NaBH 4 under Microwave Irradiation . Journal of the Chinese Chemical Society 52:6, pages 1179-1184.
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Behzad Zeynizadeh. (2005) Titanyl Acetylacetonate as an Efficient Catalyst for Regioselective 1,2-Reduction of α,β-Unsaturated Carbonyl Compounds and Conversion of α-Diketones & Acyloins to Vicinal Diols with Sodium Borohydride. Journal of the Chinese Chemical Society 52:3, pages 525-530.
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Behzad Zeynizadeh & Tarifeh Behyar. (2005) Wet THF as a Suitable Solvent for a Mild and Convenient Reduction of Carbonyl Compounds with NaBH4. Bulletin of the Chemical Society of Japan 78:2, pages 307-315.
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. (2003) A Mild and Convenient Method for the Reduction of Carbonyl Compounds with NaBH 4 in the Presence of Catalytic Amounts of MoCl 5 . Bulletin of the Korean Chemical Society 24:11, pages 1664-1670.
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. (2003) (Pyridine)(tetrahydroborato)zinc Complex, [Zn(BH 4 ) 2 (py)], as a New Stable, Efficient and Chemoselective Reducing Agent for Reduction of Carbonyl Compounds . Bulletin of the Korean Chemical Society 24:4, pages 453-459.
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. (2003) Mild and Efficient Reduction of α,β-Unsaturated Carbonyl Compounds, α-Diketones and Acyloins with Sodium Borohydride/Dowex1-x8 System. Bulletin of the Korean Chemical Society 24:3, pages 295-298.
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Luca Banfi, Enrica Narisano & Renata Riva. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis.
Peter Rittmeyer & Ulrich Wietelmann. 2000. Ullmann's Encyclopedia of Industrial Chemistry. Ullmann's Encyclopedia of Industrial Chemistry.
Leonid N Zanaveskin, Vyacheslav A Aver'yanov & Yurii A Treger. (1996) Prospects for the development of methods for the processing of organohalogen waste. Characteristic features of the catalytic hydrogenolysis of halogen-containing compounds. Russian Chemical Reviews 65:7, pages 617-624.
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Joseph C. Fuller, Eric L. Stangeland, Christian T. Goralski & Bakthan Singaram. (1993) Aminoborohydrides. 2. Regiospecific reductions of α, β-unsaturated carbonyl compounds with lithium pyrrolidinoborohydride. A facile conversion of α, β-unsaturated aldehydes and ketones to the corresponding allylic alcohols in high purity. Tetrahedron Letters 34:2, pages 257-260.
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Takuo Nishida, Takuya Nihira & Yasuhiro Yamada. (1991) Facile synthesis of racemic 2-hexyl-3-Hydroxy-4-pentanolide(NFX-2) and its optical resolution. Tetrahedron 47:33, pages 6623-6634.
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Jean-Claude Blazejewski, Frédéric Le Guyader & Claude Wakselman. (1991) The angular trifluoromethyl group. Part 4. Synthesis of the 9,9,9-trifluoro analogue of the Wieland–Miescher ketone. J. Chem. Soc., Perkin Trans. 1:5, pages 1121-1125.
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R. S. Cowles, J. R. Miller, R. M. Hollingworth, M. T. Abdel-Aal, F. Szurdoki, K. Bauer & G. Matolcsy. (1990) Cinnamyl derivatives and monoterpenoids as nonspecific ovipositional deterrents of the onion fly. Journal of Chemical Ecology 16:8, pages 2401-2428.
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R. S. VARMA & G. W. KABALKA. (2016) ChemInform Abstract: Allylic Alcohols via the Chemoselective Reduction of Enone Systems with Sodium Borohydride in Methanolic Tetrahydrofuran.. Chemischer Informationsdienst 17:4.
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