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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 27, 1997 - Issue 4
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Original Articles

The Synthesis of Allyl Selenides by Organosamarium Reagent

Mingxin Yu Department of Chemistry, Hangzhou University, Hangzhou, 310028, P.R. China
,
Yongmin Zhang Department of Chemistry, Hangzhou University, Hangzhou, 310028, P.R. China
&
Weiliang Bao Department of Chemistry, Hangzhou University, Hangzhou, 310028, P.R. China
Pages 609-613 | Received 03 Jul 1996, Published online: 20 Aug 2006

Citations (18)

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Read on this site (2)

You Huang & Ruyu Chen. (2000) A Novel Synthesis of Allyl Selenides by Reaction of an Organosamarium Reagent With Alkyl Selenocyanates. Synthetic Communications 30:2, pages 377-381.
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Xian Huang & Xin-Hua Xu. (1998) A New Method for the Synthesis of Allyl Arylselenides via the Reaction of the Zinc Allyl Selenoates with Diaryliodonium Salts. Synthetic Communications 28:5, pages 801-805.
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Articles from other publishers (16)

Sanjio S. Zade & Harkesh B. Singh. 2009. PATAI'S Chemistry of Functional Groups. PATAI'S Chemistry of Functional Groups.
Selvan Demir, Thomas J. Mueller, Joseph W. Ziller & William J. Evans. (2011) σ Bond Metathesis Reactivity of Allyl Scandium Metallocenes with Diphenyldichalcogenides, PhEEPh (E = S, Se, Te). Organometallics 30:11, pages 3083-3089.
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Yun-kui Liu, Dan-qian Xu, Zhen-yuan Xu & Yong-min Zhang. (2006) A convenient and stereoselective synthesis of (Z)-allyl selenides via Sm/TMSCl system-promoted coupling of Baylis-Hillman adducts with diselenides. Journal of Zhejiang University SCIENCE B 7:5, pages 393-396.
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T. Kataoka & S. Watanabe. 2005. Comprehensive Organic Functional Group Transformations II. Comprehensive Organic Functional Group Transformations II 237 254 .
Xingliang Zheng & Yongmin Zhang. (2019) Highly Regioselective Nucleophilic Addition of the Allylsamarium Bromide to α, β-Unsaturated Alkynones. Journal of Chemical Research 2003:8, pages 472-473.
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Zhifang Li & Yongmin Zhang. (2019) The Synthesis of N-(1-Allyl-3-Butenyl)-N-Aryl Amines by Addition of Organosamarium Reagents to Formanilides. Journal of Chemical Research 2002:6, pages 297-298.
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Wei‐Ke Su, Yong‐Shu Li, Yong‐Min Zhang & Yun‐Fa Zheng. (2010) Facile Formation of Ytterbium Diiodide and Its Use in the Synthesis of Allyl Selenides. Chinese Journal of Chemistry 20:2, pages 174-177.
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Yunkui Liu & Yongmin Zhang. (2019) Tetrahydrofuran Ring Opening with Acyloxyphosphonium Bromide Catalysed by Allylsamarium Bromide: A Novel and Effective Method for the Preparation of 4-Bromobutyl Esters. Journal of Chemical Research 2002:1, pages 15-16.
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Jue Chen & Yong‐Min Zhang. (2010) Facile Preparation of Homoallyl β',γ'‐Unsaturated Amines via 1, 2‐Addition of α, β‐Unsaturated Imines with Allylsamarium Bromide. Chinese Journal of Chemistry 20:1, pages 103-106.
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Yuri‐Fa Zheng, Hong‐Yun Guo & Yong‐Min Zhang. (2010) Synthesis of Allyl Selenides Promoted by an Sm/ZnCl 2 Bimetal System in the Presence of Water . Chinese Journal of Chemistry 19:5, pages 530-532.
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Wei‐Ke Su, Yong‐Min Zhang & Yong‐Shu Li. (2010) Allylation of Diselenides, Aldehydes and Ketones with Ytterbium/Allyl Bromide System. Chinese Journal of Chemistry 19:4, pages 381-385.
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Abhijit Kundu & Sujit Roy. (1999) Copper(II)/Tin(II) Reagent for Allylation, Propargylation, Alkynylation, and Benzylation of Diselenides:  A Novel Bimetallic Reactivity. Organometallics 19:1, pages 105-107.
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Weiliang Bao, Yunfa Zheng & Yongmin Zhang. (2019) Conjugate Addition of Organosamarium Reagents to Nitroalkenes. Journal of Chemical Research 23:12, pages 732-733.
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Zhuangping Zhan, Genliang Lu & Yongmin Zhang. (2019) A Novel Synthesis of Allyl Sulfides and Allyl Selenides via Sm–BiCl 3 System in Aqueous Media . Journal of Chemical Research 23:4, pages 280-281.
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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.
Crossref
M. YU, Y. ZHANG & W. BAO. (2010) ChemInform Abstract: The Synthesis of Allyl Selenides by Organosamarium Reagent.. ChemInform 28:26.
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