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Reformatsky reaction (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Reformatsky reaction" in English language version.

refsWebsite
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25doi.org
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5nih.gov
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1zenodo.org
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1semanticscholar.org
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doi.org

  • Reformatsky, S. (1887). "Neue Synthese zweiatomiger einbasischer Säuren aus den Ketonen". Berichte der Deutschen Chemischen Gesellschaft. 20 (1): 1210–1211. doi:10.1002/cber.188702001268.
  • Shriner, R. L. (1942). "The Reformatsky Reaction". Organic Reactions. 1: 1–37. doi:10.1002/0471264180.or001.01. ISBN 9780471264187.
  • Rathke, M. W. (1975). "The Reformatsky Reaction". Organic Reactions. 22: 423–460. doi:10.1002/0471264180.or022.04. ISBN 0471264180.
  • Sato, Toshio; Itoh, Toshiyuki; Fujisawa, Tamotsu (1982). "Facile synthesis of β-ketoesters by a coupling reaction of the Reformatsky reagent with acyl chlorides catalyzed by a palladium complex". Chemistry Letters. 11 (10): 1559–1560. doi:10.1246/cl.1982.1559.
  • Gilman, Henry; Speeter, Merrill (1943). "The Reformatsky Reaction with Benzalaniline". Journal of the American Chemical Society. 65 (11): 2255–2256. doi:10.1021/ja01251a503.
  • Stamm, H.; Steudle, H. (1979). "Nitrone—XI Isoxazolidin-verbindungen—VIII : N-substituierte 5-isoxazolidinone durch reformatzky-reaktion mit nitronen". Tetrahedron. 35 (5): 647–650. doi:10.1016/0040-4020(79)87010-6.
  • Moriwake, Tosio (1966). "The Reformatsky Reaction. I. Condensation of Ketones and t-Butyl Bromoacetate by Magnesium". The Journal of Organic Chemistry. 31 (3): 983–985. doi:10.1021/jo01341a524.
  • Liu, Xuan-Yu; Li, Xiang-Rui; Zhang, Chen; Chu, Xue-Qiang; Rao, Weidong; Loh, Teck-Peng; Shen, Zhi-Liang (2019). "Iron(0)-Mediated Reformatsky Reaction for the Synthesis of β-Hydroxyl Carbonyl Compounds". Organic Letters. 21 (15): 5873–5878. doi:10.1021/acs.orglett.9b01999. PMID 31318222. S2CID 197541600.
  • Orsini, Fulvia; Pelizzoni, Francesca; Pulici, Maurizio; Vallarino, Lidia M. (1994). "A cobalt-phosphine complex as mediator in the formation of carbon-carbon bonds". The Journal of Organic Chemistry. 59 (1): 1–3. doi:10.1021/jo00080a001.
  • Inaba, Shin-ichi; Rieke, Reuben D. (1985). "Reformatsky type additions of haloacetonitriles to aldehydes mediated by metallic nickel". Tetrahedron Letters. 26 (2): 155–156. doi:10.1016/S0040-4039(00)61867-1.
  • Kagoshima, Hirotaka; Hashimoto, Yukihiko; Oguro, Dai; Saigo, Kazuhiko (1998). "An Activated Germanium Metal-Promoted, Highly Diastereoselective Reformatsky Reaction". The Journal of Organic Chemistry. 63 (3): 691–697. doi:10.1021/jo971672j. PMID 11672062.
  • Burkhardt, Elizabeth R.; Rieke, Reuben D. (1985). "The direct preparation of organocadmium compounds from highly reactive cadmium metal powders". The Journal of Organic Chemistry. 50 (3): 416–417. doi:10.1021/jo00203a036.
  • Chao, Li-Chung; Rieke, Reuben D. (1975). "Activated metals. IX. New reformatsky reagent involving activated indium for the preparation of β-hydroxy esters". The Journal of Organic Chemistry. 40 (15): 2253–2255. doi:10.1021/jo00903a031.
  • Araki, Shuki; Ito, Hirokazu; Butsugan, Yasuo (1988). "Synthesis of β-Hydroxyesters by Reformatsky Reaction Using Indium Metal". Synthetic Communications. 18 (4): 453–458. doi:10.1080/00397918808064009.
  • Yanagisawa, Akira; Takahashi, Hiroshi; Arai, Takayoshi (2004). "Reactive barium-promoted Reformatsky-type reaction of α-chloroketones with aldehydes". Chemical Communications (5): 580–581. doi:10.1039/B314752P. PMID 14973617.
  • Imamoto, Tsuneo; Kusumoto, Tetsuo; Tawarayama, Yoshinori; Sugiura, Yasushi; Mita, Takeshi; Hatanaka, Yasuo; Yokoyama, Masataka (1984). "Carbon-carbon bond-forming reactions using cerium metal or organocerium(III) reagents". The Journal of Organic Chemistry. 49 (21): 3904–3912. doi:10.1021/jo00195a006.
  • Tabuchi, Takanori; Kawamura, Kisa; Inanaga, Junji; Yamaguchi, Masaru (1986). "Preparation of medium- and large-ring lactones. SmI2-induced cyclization of ω-(α-bromoacyloxy) aldehydes". Tetrahedron Letters. 27 (33): 3889–3890. doi:10.1016/S0040-4039(00)83907-6.
  • Molander, Gary A.; Etter, Jeffrey B. (1987). "Lanthanides in organic synthesis. 8. 1.3-Asymmetric induction in intramolecular Reformatskii-type reactions promoted by samarium diiodide". Journal of the American Chemical Society. 109 (21): 6556–6558. doi:10.1021/ja00255a076.
  • Dubois, Jacques-Emile; Axiotis, Georges; Bertounesque, Emmanuel (1985). "Chromium (II) chloride : a new reagent for cross-aldol reactions". Tetrahedron Letters. 26 (36): 4371–4372. doi:10.1016/S0040-4039(00)98737-9.
  • Ishihara, Takashi; Yamanaka, Tohru; Ando, Teiichi (1984). "New low-valent titanium catalyzed reaction of chlorodifluoromethyl ketones leading to α,α-difluorinated β-hydroxy ketones". Chemistry Letters. 13 (7): 1165–1168. doi:10.1246/cl.1984.1165.
  • Fukuzawa, Shin-Ichi; Fujinami, Tatsuo; Sakai, Shizuyoshi (1985). "Carbon–carbon bond formation between α-halogenoketones and aldehydes promoted by cerium(III) iodide or cerium(III) chloride–sodium iodide". Journal of the Chemical Society, Chemical Communications (12): 777–778. doi:10.1039/C39850000777.
  • Parrish, J. D.; Shelton, Daniel R.; Little, R. Daniel (2003). "Titanocene(III)-Promoted Reformatsky Additions". Organic Letters. 5 (20): 3615–3617. doi:10.1021/ol035269c. PMID 14507186.
  • Dekker, J.; Budzelaar, P. H. M.; Boersma, J.; van der Kerk, G. J. M. & Spek, A. J. (1984). "The Nature of the Reformatsky Reagent. Crystal Structure of (BrZnCH2COO-t-Bu · THF)2". Organometallics. 9 (3): 1403–1407. doi:10.1021/om00087a015.
  • Miki, S.; Nakamoto, K.; Kawakami, J.; Handa, S.; Nuwa, S. (2008). "The First Isolation of Crystalline Ethyl Bromozincacetate, Typical Reformatsky Reagent: Crystal Structure and Convenient Preparation". Synthesis. 2008 (3): 409–412. doi:10.1055/s-2008-1032023.
  • Lambert, T. H.; Danishefsky, S. J. (2006). "Total Synthesis of UCS1025A". Journal of the American Chemical Society. 128 (2): 426–427. doi:10.1021/ja0574567. PMID 16402826.

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  • Reformatsky, S. (1887). "Neue Synthese zweiatomiger einbasischer Säuren aus den Ketonen". Berichte der Deutschen Chemischen Gesellschaft. 20 (1): 1210–1211. doi:10.1002/cber.188702001268.