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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 18, 1988 - Issue 16-17
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Original Articles

An Aldol-Like Reaction Mediated by SmI2

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Pages 2003-2010 | Published online: 05 Dec 2006

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (7)

Heung Soo Baek, Byung Woo Yoo, Sam Rok Keum, Cheol Min Yoon, Sung Hoon Kim & Joong Hyup Kim. (2000) Synthesis of 1,3-Diketones by Reaction of α-Haloketones with Acyl Cyanides Promoted by Samarium Diiodide. Synthetic Communications 30:1, pages 31-38.
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Lei Wang & Yongmin Zhang. (1998) Sm(Hg) Promoted Pinacolic Coupling of Aromatic Aldehydes and Ketones. Synthetic Communications 28:21, pages 3991-3997.
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Junquan Wang Yongmin Zhang & Weiliang Bao. (1996) Allylation of Imines with Samarium/Allyl Bromide System. Synthetic Communications 26:13, pages 2473-2477.
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T. Arime, H. Takahashi, S. Kobayashi, S. Yamaguchi & N. Mori. (1995) Sml2 or Sml3 Mediated Aldol-Type Reaction of α-Halo Ketones with Aliphatic α-Diketones: Facile Synthesis of 2-Hydroxy-1, 4-diketones. Synthetic Communications 25:3, pages 389-393.
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Tsutomu Arime, Naoki Kato, Fumio Komadate, Hiroko Saegusa & Nobuo Mori. (1994) Aldol-Type Reaction of α-Halo Ketones with α-Ketocarboxylates Mediated by SmI2 or SmI3: Facile Synthesis of α-Hydroxy-γ-ketocarboxylates. Synthetic Communications 24:22, pages 3315-3319.
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Articles from other publishers (23)

Louis F. Fieser, Mary Fieser & Tse‐Lok HoTse‐Lok Ho, Mary Fieser, Louis Fieser & 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 & 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 & Janice Smith. 2006. Fieser and Fieser's Reagents for Organic Synthesis. Fieser and Fieser's Reagents for Organic Synthesis 444 446 .
Louis F. Fieser, Mary Fieser & Tse‐Lok HoTse‐Lok Ho, Mary Fieser, Louis Fieser & Janice Smith. 2006. Fieser and Fieser's Reagents for Organic Synthesis. Fieser and Fieser's Reagents for Organic Synthesis 507 513 .
Louis F. Fieser, Mary Fieser & Tse‐Lok HoTse‐Lok Ho, Mary Fieser, Louis Fieser & 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 & 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 & Janice Smith. 2006. Fieser and Fieser's Reagents for Organic Synthesis. Fieser and Fieser's Reagents for Organic Synthesis.
Xuesen Fan, Xinying Zhang & Yongmin Zhang. (2019) SmI 2 -mediated reduction of phenacyl azides: A novel preparation of 2,4-diarylpyrroles . Journal of Chemical Research 2005:11, pages 750-752.
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Steffen Breitfelder, Anne C. Schuemacher, Thomas Rölle, Makoto Kikuchi & Reinhard W. Hoffmann. (2004) Synthesis of Pederic Acid and Related Model Studies. Helvetica Chimica Acta 87:5, pages 1202-1213.
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Lei Wang, Pinhua Li & Li Zhou. (2002) A novel reduction of sodium alkyl thiosulfates using samarium metal without an activating agent in water. Tetrahedron Letters 43:45, pages 8141-8143.
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Xuesen Fan & Yongmin Zhang. (2002) SmI 2 -mediated synthesis of 2,4-diarylpyrroles from phenacyl azides. Tetrahedron Letters 43:10, pages 1863-1865.
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Yun‐Kui Liu, Yong‐Min Zhang & Xi Liu. (2010) Intermolecular Heterocoupling Reaction between N‐Sulfonylimines and Aliphatic Ketones Promoted by Samarium (II) Iodide. Chinese Journal of Chemistry 19:5, pages 500-503.
Crossref
Alois Fürstner. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis.
Lei Wang & Yongmin Zhang. (1999) Metallic samarium promoted reductive dimerization cyclization of gem-diactivated alkenes, reductive debromination of vic-dibromides, and reduction of sodium alkyl thiosulfates in aqueous media. Tetrahedron 55:35, pages 10695-10712.
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Alain Krief & Anne-Marie Laval. (1999) Coupling of Organic Halides with Carbonyl Compounds Promoted by SmI 2 , the Kagan Reagent . Chemical Reviews 99:3, pages 745-778.
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Ling Lu, Hung-Yu Chang & Jim-Min Fang. (1999) Samarium Ion-Promoted Cross-Aldol Reactions and Tandem Aldol/Evans−Tishchenko Reactions. The Journal of Organic Chemistry 64:3, pages 843-853.
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Ming‐Xin Yu, Yong‐Min Zhang & Wei‐Liang Bao. (2010) Application of samarium reagents in organic synthesis. Chinese Journal of Chemistry 17:1, pages 4-15.
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Shyh-Ming Yang & Jim-Min Fang. (1997) Reductive double electrophilic reactions of methyl thiophenecarboxylate mediated by samarium diiodide and hexamethylphosphoramide. Tetrahedron Letters 38:9, pages 1589-1592.
Crossref
Taokai Ying, Weiliang Bao, Yongmin Zhang & Weinming Xu. (1996) An alternative route to 1,3-diketones promoted by samarium diiodide. Tetrahedron Letters 37:22, pages 3885-3886.
Crossref
Gary A. Molander & Christina R. Harris. (1996) Sequencing Reactions with Samarium(II) Iodide. Chemical Reviews 96:1, pages 307-338.
Crossref
Yu Yongping, Lin Ronghui & Zhang Yongmin. (1993) Carboncarbon double bond formation between α—haloketones and aldehydes promoted by samarium triiodide. Tetrahedron Letters 34:28, pages 4547-4550.
Crossref
. 1992. Compendium of Organic Synthetic Methods. Compendium of Organic Synthetic Methods 298 485 .
Y. ZHANG, T. LIU & R. LIN. (1989) ChemInform Abstract: An Aldol-Like Reaction Mediated by SmI2.. ChemInform 20:17.
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