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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 12, 1982 - Issue 13
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Original Articles

Simple Preparation of 1-Bromo-1-Trimethylsilyl-1(Z), 4-pentadiene and its Use as 4-Pentenoyl Anion Equivalent

R. Yamaguchi Department of Industrial Chemistry, Faculty of Engineering, Kyoto University, Kyoto, 606, Japan
,
H. Kawasaki Department of Industrial Chemistry, Faculty of Engineering, Kyoto University, Kyoto, 606, Japan
&
M. Kawanisi Department of Industrial Chemistry, Faculty of Engineering, Kyoto University, Kyoto, 606, Japan
Pages 1027-1037 | Published online: 06 Dec 2006

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Dipanjan Pan, Gandhi K. Kar & Jayanta K. Ray. (2003) Indium Mediated Allylation of β-Chloro-/β-Alkoxy Vinylaldehyde: A Facile One Pot Synthesis of 1-Chloro-/1-Alkoxy Hexa-1,5-diene-3-ol Derivatives. Synthetic Communications 33:1, pages 1-9.
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Articles from other publishers (21)

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Xiaojun Zeng, Zhichao Lu, Shiwen Liu, Gerald B. Hammond & Bo Xu. (2017) Metal-free, Regio-, and Stereo-Controlled Hydrochlorination and Hydrobromination of Ynones and Ynamides. The Journal of Organic Chemistry 82:24, pages 13179-13187.
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David A. Petrone, Juntao Ye & Mark Lautens. (2016) Modern Transition-Metal-Catalyzed Carbon–Halogen Bond Formation. Chemical Reviews 116:14, pages 8003-8104.
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Xiao-Yu Lu, Jing-Hui Liu, Xi Lu, Zheng-Qi Zhang, Tian-Jun Gong, Bin Xiao & Yao Fu. (2016) 1,1-Disubstituted olefin synthesis via Ni-catalyzed Markovnikov hydroalkylation of alkynes with alkyl halides. Chemical Communications 52:30, pages 5324-5327.
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Takami Morishita, Hiroto Yoshida & Joji Ohshita. (2010) Copper-catalysed bromoalkynylation of arynes. Chem. Commun. 46:4, pages 640-642.
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Louis F. Fieser, Mary Fieser & Tse‐Lok HoTse‐Lok Ho, Mary Fieser & Louis Fieser. 2006. Fieser and Fieser's Reagents for Organic Synthesis. Fieser and Fieser's Reagents for Organic Synthesis.
Dipanjan Pan, Sajal K Mal, Gandhi K Kar & Jayanta K Ray. (2002) Chemoselective method for the synthesis of 4-allyl-4-hydroxycyclohexa-2,5-dienone derivatives from 1,4-quinones by an indium-mediated allylation protocol. Tetrahedron 58:14, pages 2847-2852.
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Helen T. Lee. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis.
Khalid Bougrin, André Loupy, Alain Petit, Rachid Benhida, Jean-Louis Fourrey, Boujemâa Daou & Mohamed Soufiaoui. (2000) N-Trifluoroacétylation sélective d'ortho-arylènediamines sous ultrasons. Tetrahedron Letters 41:25, pages 4875-4879.
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Khalid Bougrin, Mustapha Lamiri & Mohamed Soufiaoui. (1998) Synthèse “one pot”de dérivés isoxazoliniques par activation sonochimique. Tetrahedron Letters 39:25, pages 4455-4458.
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Jean-Louis LuchePedro Cintas & Jean-Louis Luche. 1998. Synthetic Organic Sonochemistry. Synthetic Organic Sonochemistry 167 234 .
Hai-Shan Dang & Brian P. Roberts. (1996) Radical addition to carbenoids. Chain reactions of α-diazo carbonyl compounds with triorganotin hydrides, tris(trimethylsilyl)silane and allyltributylstannane. J. Chem. Soc., Perkin Trans. 1:8, pages 769-775.
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Jean‐Louis Luche & Pedro Cintas. 1995. Active Metals. Active Metals 133 190 .
Basil J. Wakefield. 1995. Organomagnesium Methods in Organic Synthesis. Organomagnesium Methods in Organic Synthesis 151 180 .
. 1995. Comprehensive Organic Functional Group Transformations. Comprehensive Organic Functional Group Transformations 1085 1229 .
David I. Smith. 1995. Comprehensive Organic Functional Group Transformations. Comprehensive Organic Functional Group Transformations 789 822 .
Bruce H. Lipshutz & Saumitra Sengupta. 2004. Organic Reactions. Organic Reactions 135 631 .
David J. Ager. 2004. Organic Reactions. Organic Reactions 1 223 .
Ian Fleming, Jacques Dunoguès & Roger Smithers. 2004. Organic Reactions. Organic Reactions 57 575 .
Penny A. Chaloner. (1988) Nickel, Palladium and Platinum. Annual survey covering the year 1982. Journal of Organometallic Chemistry 357:1-3, pages 51-246.
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R. YAMAGUCHI, H. KAWASAKI & M. KAWANISI. (2016) ChemInform Abstract: SIMPLE PREPARATION OF 1‐BROMO‐1‐TRIMETHYLSILYL‐1(Z), 4‐PENTADIENE AND ITS USE AS 4‐PENTENOYL ANION EQUIVALENT. Chemischer Informationsdienst 14:28.
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