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Simmonsova–Smithova reakce (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Simmonsova–Smithova reakce" in Czech language version.

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  • Howard Ensign Simmons; R. D. Smith. A New Synthesis of Cyclopropanes from Olefins. Journal of the American Chemical Society. 1958, s. 5323–5324. doi:10.1021/ja01552a080. 
  • H. E. Simmons; R. D. Smith. A New Synthesis of Cyclopropanes. Journal of the American Chemical Society. 1959, s. 4256–4264. doi:10.1021/ja01525a036. 
  • J. M. Denis; J. M. Denis; J. M. Conia. Improved Simmons–Smith Reactions. Synthesis. 1972, s. 549–551. doi:10.1055/s-1972-21919. 
  • A. B. Charette; A. Beauchemin. Simmons-Smith Cyclopropanation Reaction. Organic Reactions. 2001, s. 1. ISBN 978-0471264187. doi:10.1002/0471264180.or058.01. 
  • Bodo Fabisch; Terence N. Mitchell. An inexpensive modification of the Simmons-Smith reaction: The formation of bromomethylzinc bromide as studied by NMR spectroscopy. Journal of Organometallic Chemistry. 1984, s. 219–221. doi:10.1016/0022-328X(84)80305-8. 
  • Georg Wittig; Frank Wingler. Über methylenierte Metallhalogenide, IV. Cyclopropan-Bildung aus Olefinen mit Bis-halogenmethyl-zink. Chemische Berichte. 1964, s. 2146–2164. doi:10.1002/cber.19640970808. 
  • J. Furukawa; N. Kawabata; J. Nishimura. Synthesis of cyclopropanes by the reaction of olefins with dialkylzinc and methylene iodide. Tetrahedron. 1968, s. 53–58. doi:10.1016/0040-4020(68)89007-6. 
  • Howard E. Simmons; Theodore L. Cairns; Susan A. Vladuchick; Connie M. Hoiness. Cyclopropanes from Unsaturated Compounds, Methylene Iodide, and Zinc-Copper Couple. Organic Reactions. 2011-03-15. Dostupné online. ISBN 978-0471264187. doi:10.1002/0471264180.or020.01. 
  • Paul A. Grieco; Tomei Oguri; Chia-Lin J. Wang; Eric Williams. Stereochemistry and total synthesis of (±)-ivangulin. The Journal of Organic Chemistry. 1977, s. 4113–4118. doi:10.1021/jo00445a027. 
  • Hideyo Takahashi; Masato Yoshioka; Masaji Ohno; Susumu Kobayashi. A catalytic enantioselective reaction using a C2-symmetric disulfonamide as a chiral ligand: cyclopropanation of allylic alcohols by the Et2Zn-CH2I2-disulfonamide system. Tetrahedron Letters. 1992, s. 2575–2578. doi:10.1016/S0040-4039(00)92246-9. 
  • Tao Wang; Yong Liang; Zhi-Xiang Yu. Density Functional Theory Study of the Mechanism and Origins of Stereoselectivity in the Asymmetric Simmons–Smith Cyclopropanation with Charette Chiral Dioxaborolane Ligand. Journal of the American Chemical Society. 2011, s. 9343–9353. doi:10.1021/ja111330z. PMID 21627114. 
  • Hiroaki Shitama; Tsutomu Katsuki. Asymmetric Simmons–Smith Reaction of Allylic Alcohols with Al Lewis Acid/N Lewis Base Bifunctional Al(Salalen) Catalyst. Angewandte Chemie International Edition. 2008, s. 2450–2453. doi:10.1002/anie.200705641. PMID 18288666. 
  • S. E. Denmark; J. P. Edwards. A Comparison of (Chloromethyl)- and (Iodomethyl)zinc Cyclopropanation Reagents. The Journal of Organic Chemistry. 1991, s. 6974–6981. doi:10.1021/jo00025a007. 
  • G. M. Rubottom; M. I. Lopez. Reaction of Trimethysilyl Enol Ethers with Simmons-Smith Reagent. Facile Synthesis of Trimethylsilyl Cyclopropyl Ethers and Cyclopropanols. The Journal of Organic Chemistry. 1973, s. 2097–2099. doi:10.1021/jo00951a032. 
  • E. C. Friedrich; F. Niyati-Shirkhodaee. Regioselectivity and Solvent Effects in Cyclopropanation of Alkadienes. The Journal of Organic Chemistry. 1991, s. 2202–2205. doi:10.1021/jo00006a044. 
  • J. Lee; H. Kim; J. K. Cha. Diastereoselective Synthesis of Cis-1,2-Dialkenylcyclopropanols and Subsequent Oxy-Cope Rearrangement. Journal of the American Chemical Society. 1995, s. 9919–9920. doi:10.1021/ja00144a022. 
  • I. M. Takakis; Y. E. Rhodes. Diastereoselective Cyclopropanation of Some Simple Olefinic Compounds. By-Product Formation in Excess Simmons-Smith Reagent. The Journal of Organic Chemistry. 1978, s. 3496–3500. doi:10.1021/jo00412a017. 
  • T. Cohen; Z. Kosarych. Complete regio- and stereospecificity in the Lewis acid catalyzed Diels-Alder reactions of (Z)-2-methoxy-1-(phenylthio)-1,3-butadienes. Conversion of the CS configuration of an adduct to the CC configuration at the allylic position by a [2,3] sigmatropic rearrangement. The Journal of Organic Chemistry. 1982, s. 4005–4008. doi:10.1021/jo00141a047. 
  • Éric Lévesque; Sébastien R. Goudreau; André B. Charette. Improved Zinc-Catalyzed Simmons–Smith Reaction: Access to Various 1,2,3-Trisubstituted Cyclopropanes. Organic Letters. 2014, s. 1490–1493. doi:10.1021/ol500267w. PMID 24555697. 
  • G. A. Molander; L. S. Harring. Samarium-Promoted Cyclopropanation of Allylic Alcohols. The Journal of Organic Chemistry. 1989, s. 3525–3532. doi:10.1021/jo00276a008. 
  • K. Maruoka; Y. Fukutani; H. Yamamoto. Trialkylaluminum-Alkylidene Iodide. A Powerful Cyclopropanation Agent with Unique Selectivity. The Journal of Organic Chemistry. 1985, s. 4412–4414. doi:10.1021/jo00222a051. 
  • Yashoda Bhogadhi; Charles Zercher. Discussion Addendum for: Formation of γ-Keto Esters from β-Keto Esters: Methyl 5,5-dimethyl-4-oxohexanoate. Organic Syntheses. 2014, s. 248–259. doi:10.15227/orgsyn.091.0248. 
  • Matthew Ronsheim; Ramona Hilgenkamp; Charles Zercher. Formation of γ-Keto Esters from β-Keto Esters: Methyl 5,5-dimethyl-4-oxohexanoate. Organic Syntheses. 2002, s. 146. Dostupné online. ISBN 978-0471264224. doi:10.1002/0471264180.os079.18. 
  • Yong-Chua Teo; Richard Hsung. Discussion Addendum for: Practical Synthesis of Novel Chiral Allenamides: (R)-4- Phenyl-3-(1,2-propadienyl)oxazolidin-2-one. Organic Syntheses. 2014, s. 12–26. doi:10.15227/orgsyn.091.0012. 
  • H. Xiong; M. Tracey; T. Grebe; J. Mulder; R. Hsung. PRACTICAL SYNTHESIS OF NOVEL CHIRAL ALLENAMIDES: (R)-4-PHENYL-3-(1,2-PROPADIENYL)OXAZOLIDIN-2-ONE (2-Oxazolidinone, 4-phenyl-3-(1,2-propadienyl)–, (4R)–). Organic Syntheses. 2005, s. 147–156. doi:10.15227/orgsyn.081.0147. 
  • William Donaldson. Synthesis of cyclopropane containing natural products. Tetrahedron. 2001-10-08, s. 8589. Dostupné online. doi:10.1016/s0040-4020(01)00777-3. 
  • Synthesis of SUVN-911. Synfacts. 2020, s. 0626. ISSN 1861-1958. doi:10.1055/s-0040-1707534. 

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  • Tao Wang; Yong Liang; Zhi-Xiang Yu. Density Functional Theory Study of the Mechanism and Origins of Stereoselectivity in the Asymmetric Simmons–Smith Cyclopropanation with Charette Chiral Dioxaborolane Ligand. Journal of the American Chemical Society. 2011, s. 9343–9353. doi:10.1021/ja111330z. PMID 21627114. 
  • Hiroaki Shitama; Tsutomu Katsuki. Asymmetric Simmons–Smith Reaction of Allylic Alcohols with Al Lewis Acid/N Lewis Base Bifunctional Al(Salalen) Catalyst. Angewandte Chemie International Edition. 2008, s. 2450–2453. doi:10.1002/anie.200705641. PMID 18288666. 
  • Éric Lévesque; Sébastien R. Goudreau; André B. Charette. Improved Zinc-Catalyzed Simmons–Smith Reaction: Access to Various 1,2,3-Trisubstituted Cyclopropanes. Organic Letters. 2014, s. 1490–1493. doi:10.1021/ol500267w. PMID 24555697. 

orgsyn.org

  • SMITH, R. D.; SIMMONS, H. E. Norcarane. Org. Synth.. Dostupné online. ; Coll. Vol.. S. 855. 
  • ITO, Y.; FUJII, S.; NAKATUSKA, M.; KAWAMOTO, F.; SAEGUSA, T. One-Carbon Ring Expansion Of Cycloalkanones To Conjugated Cycloalkenones: 2-Cyclohepten-1-one. Org. Synth.. 1988. Dostupné online. ; Coll. Vol.. S. 327. 
  • Matthew Ronsheim; Ramona Hilgenkamp; Charles Zercher. Formation of γ-Keto Esters from β-Keto Esters: Methyl 5,5-dimethyl-4-oxohexanoate. Organic Syntheses. 2002, s. 146. Dostupné online. ISBN 978-0471264224. doi:10.1002/0471264180.os079.18. 

worldcat.org