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Synthetic Communications

An International Journal for Rapid Communication of Synthetic Organic Chemistry

Volume 37, 2007 - Issue 16

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Original Articles

Amination of the Baylis–Hillman Acetates in Ethanol

Young Sang Park Graduate School of Biotechnology, Korea University, South Korea

Min Young Cho Department of New Material Chemistry, Korea University, South Korea

Young Bum Kwon Department of New Material Chemistry, Korea University, South Korea

Byung Woo Yoo Department of New Material Chemistry, Korea University, South Korea

Cheol Min Yoon Department of New Material Chemistry, Korea University, South KoreaCorrespondence[email protected]

Pages 2677-2685 | Received 21 Jul 2006, Published online: 14 Aug 2007

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https://doi.org/10.1080/00397910701465370

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Sonam Tashi Khom, Pranjit Saikia, Ijaz Ullah Muzaddadi, Arumugam Murugan & Nagendra Nath Yadav. (2023) Synthesis of allylamines from Baylis–Hillman acetates using DBU under solvent free condition. Monatshefte für Chemie - Chemical Monthly 154:8, pages 865-871.
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Palanisamy Banumathi & Paramasivan Rajasingh. (2022) Selective N-allylation via SN2ꞌ reaction: Synthesis, characterization, crystal structure, theoretical and biological studies of Ethyl (E)-2-(4-aminobenzene-1-sulphonylimino-thiazol-3-yl-methyl)-3-phenyl acrylate. Journal of Molecular Structure 1269, pages 133720.
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Pambingal Rajan Sruthi, P. Uma Sankar, Thachora Venu Saranya & Saithalavi Anas. (2020) Facile Synthesis of Dihydroquinolines via Palladium Catalyzed Sequential Amination and Cyclisation of Morita‐Baylis‐Hillman Alcohols. ChemistrySelect 5:43, pages 13598-13602.
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Richard C. LarockRichard C. Larock & Alexandre A. Pletnev. 2018. Comprehensive Organic Transformations. Comprehensive Organic Transformations 1 49 .

Sandeep Suryabhan Gholap, Masanori Takimoto & Zhaomin Hou. (2016) Regioselective Alkylative Carboxylation of Allenamides with Carbon Dioxide and Dialkylzinc Reagents Catalyzed by an N‐Heterocyclic Carbene–Copper Complex. Chemistry – A European Journal 22:25, pages 8547-8552.
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Kishor Chandra Bharadwaj & Dharmendra Kumar Tiwari. (2016) Double Morita–Baylis–Hillman (MBH) strategy; an intermolecular and a chemo selective intramolecular MBH reactions for 5/6 substituted, functionalized piperidine unit. Tetrahedron 72:2, pages 312-317.
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Deevi Basavaiah, Sutanuka Pal, Gorre Veeraraghavaiah & Kishor Chandra Bharadwaj. (2015) The Baylis–Hillman acetates as a source of ambiphilic molecules: a simple synthesis of 1,3-thiazinane-2-thione frameworks. Tetrahedron 71:28, pages 4659-4664.
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Yimeng Zhang, Tao Zhang, Haoqiang Zhan & Xingwei Li. (2014) Rh(III)-catalyzed synthesis of (dihydro)quinolines via the annulation of N-sulfonyl 2-aminobenzaldehydes with olefins. Chinese Journal of Catalysis 35:11, pages 1840-1845.
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Mélanie M. Lorion, Danila Gasperini, Julie Oble & Giovanni Poli. (2013) Palladium-Catalyzed Arylic/Allylic Aminations: Permutable Domino Sequences for the Synthesis of Dihydroquinolines from Morita–Baylis–Hillman Adducts. Organic Letters 15:12, pages 3050-3053.
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Qingsheng Niu, Hui Mao, Guodong Yuan, Jilong Gao, Haiquan Liu, Yawei Tu, Xiaoxia Wang & Xin Lv. (2013) Copper‐Catalyzed Domino S N 2′/Coupling Reaction: A Versatile and Facile Synthesis of Cyclic Compounds from Baylis–Hillman Acetates . Advanced Synthesis & Catalysis 355:6, pages 1185-1192.
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Hyun-Soo Kim, Sang-Jin Lee & Cheol Min Yoon. (2013) Decarboxylative Heck Reaction of Aryl Iodide with Baylis-Hillman Adduct Using Pd/C as a Catalyst in Aqueous Media. Bulletin of the Korean Chemical Society 34:1, pages 325-327.
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Yan Wang, Tao Zhang & Li Liu. (2012) Enantioselective and α ‐Regioselective Allylic Amination of Morita‐Baylis‐Hillman Acetates with Simple Aromatic Amines Catalyzed by Planarly Chiral Ligand/Palladium Catalyst . Chinese Journal of Chemistry 30:11, pages 2641-2646.
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Yan Wang, Li Liu, Dong Wang & Yong-Jun Chen. (2012) Palladium-catalyzed α-regioselective allylic amination of Morita–Baylis–Hillman acetates with simple aromatic amines. Organic & Biomolecular Chemistry 10:34, pages 6908.
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Somnath Nag & Sanjay Batra. (2011) Applications of allylamines for the syntheses of aza-heterocycles. Tetrahedron 67:47, pages 8959-9061.
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Min Shi, Feijun Wang, Mei-Xin Zhao & Yin WeiFei-jun Wang, Yin Wei & Min Shi. 2011. The Chemistry of the Morita-Baylis-Hillman Reaction. The Chemistry of the Morita-Baylis-Hillman Reaction 325 484 .

Dmytro Tymoshenko, Gyorgy Jeges & Brian T. Gregg. 2011. 27 74 .

Deevi Basavaiah, Bhavanam Sekhara Reddy & Satpal Singh Badsara. (2010) Recent Contributions from the Baylis−Hillman Reaction to Organic Chemistry. Chemical Reviews 110:9, pages 5447-5674.
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Cécile Garzon, Mireille Attolini & Michel Maffei. (2010) Synthesis of β-aminovinylphosphonates by organocatalytic nucleophilic displacement of acetate with amines. Tetrahedron Letters 51:29, pages 3772-3774.
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Kristen N. Clary, Masood Parvez & Thomas G. Back. (2010) Rearrangements and Intramolecular Diels−Alder Reactions of Normal and Vinylogous Aza-Morita−Baylis−Hillman Products Leading to Isoindoline Derivatives. The Journal of Organic Chemistry 75:11, pages 3751-3760.
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Shao-Qin Ge, Yun-Yu Hua & Min Xia. (2009) Ultrasound-promoted access to Baylis–Hillman amines. Ultrasonics Sonochemistry 16:6, pages 743-746.
Crossref

Hyun Seung Lee, Eun Sun Kim, Sung Hwan Kim & Jae Nyoung Kim. (2009) Synthesis of poly-substituted tetrahydropyridines from Baylis–Hillman adducts modified with N-allylamino group via radical cyclization. Tetrahedron Letters 50:19, pages 2274-2277.
Crossref

Valérie Declerck, Jean Martinez & Frédéric Lamaty. (2009) aza -Baylis−Hillman Reaction . Chemical Reviews 109:1, pages 1-48.
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. (2008) One-Pot Synthesis of Naphthalenes from Baylis-Hillman Adducts via Pd-Mediated Successive Allylation and Arylation. Bulletin of the Korean Chemical Society 29:12, pages 2537-2539.
Crossref

Dafeng Li, Jian Li & Xueshun Jia. (2008) Regio- and Stereoselective Synthesis of α,β-dehydro-β-amino Esters. Journal of Chemical Research 2008:8, pages 434-436.
Crossref

Young Sang Park, Min Young Cho, Young Bum Kwon, Byung Woo Yoo & Cheol Min Yoon. (2008) ChemInform Abstract: Amination of the Baylis—Hillman Acetates in Ethanol.. ChemInform 39:6.
Crossref

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Amination of the Baylis–Hillman Acetates in Ethanol

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Amination of the Baylis–Hillman Acetates in Ethanol

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