Pure and Applied Chemistry

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• Yang Shouliang, Xi Yumeng, Zhu Rong, Wang Lin, Chen Jiahua, Yang Zhen: Asymmetric Total Syntheses of Ansamacrolactams (+)-Q-1047H-A-A and (+)-Q-1047H-R-A. Org. Lett. 2013, 15, 812. <http://dx.doi.org/10.1021/ol400038h>
• Szostak Michal, Procter David J.: Jenseits von Samariumdiiodid: Perspektiven für Lanthanoid(II)-vermittelte Reduktionen. Angew. Chem. 2012, 124, 9372. <http://dx.doi.org/10.1002/ange.201201065>
• Szostak Michal, Procter David J.: Beyond Samarium Diiodide: Vistas in Reductive Chemistry Mediated by Lanthanides(II). Angew. Chem. Int. Ed. 2012, 51, 9238. <http://dx.doi.org/10.1002/anie.201201065>
• Nomoto Akihiro, Kojo Yusuke, Shiino Go, Tomisaka Yuri, Mitani Ikuko, Tatsumi Masahiko, Ogawa Akiya: Reductive carboxylation of alkyl halides with CO2 by use of photoinduced SmI2/Sm reduction system. Tetrahetron Lett 2010, 51, 6580. <http://dx.doi.org/10.1016/j.tetlet.2010.10.028>
• Gopalaiah Kovuru, Kagan Henri B.: Use of samarium diiodide in the field of asymmetric synthesis. New J Chem 2008, 32, 607. <http://dx.doi.org/10.1039/b718330p>
• Tomisaka Yuri, Tsuchii Kaname, Ogawa Akiya: A novel photoinduced reduction of haloalkanes with rare earth metals. J Alloys Comp 2006, 408-412, 427. <http://dx.doi.org/10.1016/j.jallcom.2004.11.089>
• Kagan Henri B.: Twenty five years of organic chemistry with diiodosamarium. J Alloys Comp 2006, 408-412, 421. <http://dx.doi.org/10.1016/j.jallcom.2004.11.090>
• Kabata Masayuki, Suzuki Takamasa, Takabe Kunihiko, Yoda Hidemi: SmI2-Promoted novel tandem elimination and coupling reactions of aliphatic imides with carbonyl compounds: application to the synthesis of dl-isoretronecanol. Tetrahetron Lett 2006, 47, 1607. <http://dx.doi.org/10.1016/j.tetlet.2005.12.126>
• Bochkarev Mikhail N.: Molecular compounds of “new” divalent lanthanides. Coord Chem Rev - 2004, 248, 835. <http://dx.doi.org/10.1016/j.ccr.2004.04.004>
• Sumino Yukihito, Harato Nami, Tomisaka Yuri, Ogawa Akiya: A novel photoinduced reduction system of low-valent samarium species: reduction of organic halides and chalcogenides, and its application to carbonylation with carbon monoxide. Tetrahedron 2003, 59, 10499. <http://dx.doi.org/10.1016/j.tet.2003.08.070>
• Kagan Henri B.: Twenty-five years of organic chemistry with diiodosamarium: an overview. Tetrahedron 2003, 59, 10351. <http://dx.doi.org/10.1016/j.tet.2003.09.101>
• Yoda Hidemi, Kohata Naoki, Takabe Kunihiko: A New Entry for the Preparation of Substituted Aromatic Carbonyl Compounds Mediated by Samarium(II) Iodide. Synth Common 2003, 33, 1087. <http://dx.doi.org/10.1081/SCC-120017130>
• Zhou Xigeng, Zhu Ming: Insertions into lanthanideligand bonds in organolanthanide chemistry. J Organomet Chem 2002, 647, 28. <http://dx.doi.org/10.1016/S0022-328X(01)01406-1>
• Su Weike, Yang Bibo, Zhang Yongmin: Nucleophilic substitution reactions of aminoalkylbenzotriazoles with ytterbium metal umpoled diaryl ketones. Tetrahetron Lett 2002, 43, 2251. <http://dx.doi.org/10.1016/S0040-4039(02)00235-6>
• Fan Chun-An, Wang Bao-Min, Tu Yong-Qiang, Song Zhen-Lei: Samarium-Catalyzed Tandem Semipinacol Rearrangement/Tishchenko Reaction ofα-Hydroxy Epoxides: A Novel Approach to Highly Stereoselective Construction of 2-Quaternary 1,3-Diol Units. Angew Chem 2001, 113, 3995. <http://dx.doi.org/10.1002/1521-3757(20011015)113:20<3995::AID-ANGE3995>3.0.CO;2-D>
• Fan Chun-An, Wang Bao-Min, Tu Yong-Qiang, Song Zhen-Lei: Samarium-Catalyzed Tandem Semipinacol Rearrangement/Tishchenko Reaction ofα-Hydroxy Epoxides: A Novel Approach to Highly Stereoselective Construction of 2-Quaternary 1,3-Diol Units. Angew Chem Int Ed 2001, 40, 3877. <http://dx.doi.org/10.1002/1521-3773(20011015)40:20<3877::AID-ANIE3877>3.0.CO;2-S>
• Kagan Henri B: Various aspects of the reaction of a chiral catalyst or reagent with a racemic or enantiopure substrate. Tetrahedron 2001, 57, 2449. <http://dx.doi.org/10.1016/S0040-4020(01)00065-5>
• Markó István E, Murphy Fiona, Kumps Lucien, Ates Ali, Touillaux Roland, Craig Donald, Carballares Santiago, Dolan Simon: Efficient preparation of trisubstituted alkenes using the SmI2 modification of the Julia–Lythgoe olefination of ketones and aldehydes. Tetrahedron 2001, 57, 2609. <http://dx.doi.org/10.1016/S0040-4020(01)00079-5>
• Nishiura Masayoshi, Katagiri Kosuke, Imamoto Tsuneo: Isolation, X-ray Structural Characterization, and Reactivities of Diiodosamarium(II) Complexes Bearing Amide Compounds as Ligands. Bull Chem Soc Jpn 2001, 74, 1417. <http://dx.doi.org/10.1246/bcsj.74.1417>
• Kan Toshiyuki, Nara Shinji, Ozawa Takashi, Shirahama Haruhisa, Matsuda Fuyuhiko: Hydroxy-Directed, SmI2-Induced Conversion of Carbohydrates into Carbocycles. Angew Chem 2000, 112, 363. <http://dx.doi.org/10.1002/(SICI)1521-3757(20000117)112:2<363::AID-ANGE363>3.0.CO;2-N>
• Prilezhaeva Elena N: Sulfones and sulfoxides in the total synthesis of biologically active natural compounds. RUSS CHEM REV 2000, 69, 367. <http://dx.doi.org/10.1070/RC2000v069n05ABEH000561>
• Shabangi Masangu, Sealy Jennifer M., Fuchs James R., Flowers Robert A.: The effect of cosolvent on the reducing power of SmI2 in tetrahydrofuran. Tetrahetron Lett 1998, 39, 4429. <http://dx.doi.org/10.1016/S0040-4039(98)00839-9>
• Zhou Longhu, Zhang Yongmin, Shi Daqing: Samarium(II) iodide promoted novel reductive coupling reactions of ketones and nitriles. Tetrahetron Lett 1998, 39, 8491. <http://dx.doi.org/10.1016/S0040-4039(98)01984-4>
• Corey E.J, Zheng Guo Zhu: Catalytic reactions of samarium (II) iodide. Tetrahetron Lett 1997, 38, 2045. <http://dx.doi.org/10.1016/S0040-4039(97)00263-3>
• Vogel Emanuel, Pohl Michael, Herrmann Adalbert, Wiß Torsten, König Christoph, Lex Johann, Gross Maurice, Gisselbrecht Jean Paul: Porphyrinoide Makrocyclen auf Thiophen-Basis: Octaethyltetrathiaporphyrin-Dikation. Angew Chem 1996, 108, 1677. <http://dx.doi.org/10.1002/ange.19961081345>
• Markó István E, Murphy Fiona, Dolan Simon: Efficient preparation of trisubstituted alkenes using the Julia-Lythgoe olefination of ketones. On the key-role of SmI2 in the reductive elimination step. Tetrahetron Lett 1996, 37, 2089. <http://dx.doi.org/10.1016/0040-4039(96)00200-6>
• Deelman Berth-Jan, Wierda Feike, Meetsma Auke, Teuben Jan H.: Reaction of (Cp2*LnH)2 (LnY, La) and Cp2* Y(2-C6H4CH2NME2) with esters and amides and molecular structure of [Cp2* Y (μ-OCMeCHC(OEt)O)]2. Appl Organometal Chem 1995, 9, 483. <http://dx.doi.org/10.1002/aoc.590090518>
• Dalko Peter I.: Redox induced radical and radical ionic carbon-carbon bond forming reactions. Tetrahedron 1995, 51, 7579. <http://dx.doi.org/10.1016/0040-4020(95)00434-A>
• Kang Han-Young, Sang Hong Woo, Seo Cho Yong, Yeong Koh Hun: Reductive decyanation of α-cyano and α-alkoxycarbonyl substituted nitriles promoted by samarium(II) iodide. Tetrahetron Lett 1995, 36, 7661. <http://dx.doi.org/10.1016/0040-4039(95)01606-I>
• Fadel Antoine: Optically active cyclopropanols by samarium(II) iodide induced intramolecular reductive cyclisation of β-chloro-substituted amides. Tet Asymm 1994, 5, 531. <http://dx.doi.org/10.1016/0957-4166(94)80010-3>
• Kang Han-Young, Cho Yong Seo, Koh Hun Yeong, Chang Moon Ho: Synthesis of 3-Alkylidenecepham-4-carboxylic Acid derivatives by Samarium(II) Iodide Reduction. Synth Common 1993, 23, 2977. <http://dx.doi.org/10.1080/00397919308011140>
• Rogers Robin D., Rogers Lillian M.: Lanthanides and actinides anual survey covering the years 1987–1989. J Organomet Chem 1992, 442, 83. <http://dx.doi.org/10.1016/0022-328X(92)80045-Y>
• Kamochi Yasuko, Kudo Tadahiro: Reductions of carboxylic acids and their derivatives using samarium diiodide-acid system. Tetrahedron 1992, 48, 4301. <http://dx.doi.org/10.1016/S0040-4020(01)80441-5>
• Enholm Eric J., Jiang Shujun: The conversion of α- to β-hydroxy esters by a deoxygenation/condensation reaction promoted by samarium diiodide. Tetrahetron Lett 1992, 33, 313. <http://dx.doi.org/10.1016/S0040-4039(00)74119-0>
• Kamochi Yasuko, Kudo Tadahiro: Lanthanoids in Organic Synthesis. I. The Novel Reduction of Carboxylic Acids with Samarium Diiodide-Base System. Bull Chem Soc Jpn 1992, 65, 3049. <http://dx.doi.org/10.1246/bcsj.65.3049>
• Kamochi Yasuko, Kudo Tadahiro: Reduction using samarium diiodide-base system. Tetrahetron Lett 1991, 32, 3511. <http://dx.doi.org/10.1016/0040-4039(91)80819-R>
• Künzer H., Stahnke M., Sauer G., Wiechert R.: Reductive desulfonylation of phenyl sulfones by samarium(II) iodide-hexamethylphosphoric triamide. Tetrahetron Lett 1991, 32, 1949. <http://dx.doi.org/10.1016/0040-4039(91)85009-T>
• Enholm Eric J., Satici Hikmet: A direct preparation of 1,2-diacetates from aldehydes and ketones promoted by samarium diiodide. Tetrahetron Lett 1991, 32, 2433. <http://dx.doi.org/10.1016/S0040-4039(00)74346-2>
• Sang Chul Shim, Jin-Taik Hwang, Han-Young Kang, Moon Ho Chang: Intramolecular reductive cyclization of aldehydes and ketones with alkynes promoted by Samarium(II) iodide. Tetrahetron Lett 1990, 31, 4765. <http://dx.doi.org/10.1016/S0040-4039(00)97728-1>
• Imamoto Tsuneo, Nishimura Seijiro: Samarium diiodide-promoted reductive coupling of imines. Chem Lett 1990, 1141. <http://dx.doi.org/10.1246/cl.1990.1141>