A Chiral N,N'-Dioxide-Zn(II) Complex Catalyzes the Enantioselective [2+2] Cycloaddition of Alkynones with Cyclic Enol Silyl Ethers.
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Lili Lin | Xiaoming Feng | Xiaohua Liu | Shulin Ge | Yan Lu | Tengfei Kang
[1] Auxiliadora Prieto,et al. [2+2] Cycloaddition reactions promoted by group 11 metal-based catalysts , 2016 .
[2] K. Okamoto,et al. Indium-Catalyzed [2 + 2] Cycloaddition of Allylsilanes to Internal Alkynones. , 2015, Organic letters.
[3] M. K. Brown,et al. Synthese von Cyclobutanen und Cyclobutenen: katalytische enantioselektive [2+2]‐Cycloadditionen , 2015 .
[4] M. K. Brown,et al. Cyclobutane and cyclobutene synthesis: catalytic enantioselective [2+2] cycloadditions. , 2015, Angewandte Chemie.
[5] K. Takasu,et al. An Arylative Ring Expansion Cascade of Fused Cyclobutenes via Short-Lived Intermediates with Planar Chirality. , 2015, Journal of the American Chemical Society.
[6] Lili Lin,et al. N,N′‐Dioxide/Zinc Bis(trifluoromethylsulfonyl)imide Complex Catalyzed Enantioselective Diels–Alder Reaction of Cyclopentadiene with Alkynones , 2015 .
[7] M. Nakada,et al. Highly enantioselective catalytic asymmetric [2+2] cycloadditions of cyclic α-alkylidene β-oxo imides with ynamides. , 2015, Chemistry.
[8] D. Aitken,et al. Stereoselective intermolecular [2 + 2]-photocycloaddition reactions of maleic anhydride: stereocontrolled and regiocontrolled access to 1,2,3-trifunctionalized cyclobutanes. , 2014, Organic & biomolecular chemistry.
[9] T. Bach,et al. Enantioselektive Katalyse der intermolekularen [2+2]‐Photocycloaddition von 2‐Pyridonen mit Acetylendicarbonsäureestern , 2014 .
[10] T. Bach,et al. Enantioselective catalysis of the intermolecular [2+2] photocycloaddition between 2-pyridones and acetylenedicarboxylates. , 2014, Angewandte Chemie.
[11] Lili Lin,et al. Chiral N,N′-dioxide ligands: synthesis, coordination chemistry and asymmetric catalysis , 2014 .
[12] 王刚,et al. 催化不对称[8+2]环加成反应构建环庚三烯并吡咯烷-3,3’-吲哚酮 , 2014 .
[13] A. Nishida,et al. A 2‐Benzothiazolylphenyl Group Accelerates the Intramolecular [2+2] Cycloaddition of Allene‐Ynes , 2014 .
[14] Shanshan Liu,et al. A study on the substituent effects of norbornadiene derivatives in iridium-catalyzed asymmetric [2 + 2] cycloaddition reactions. , 2013, Organic & biomolecular chemistry.
[15] F. Kakiuchi,et al. Rhodium-catalyzed intermolecular [2 + 2] cycloaddition of terminal alkynes with electron-deficient alkenes. , 2013, Organic letters.
[16] F. Rominger,et al. Vinylidengoldverbindungen: intermolekulare C(sp3)‐H‐Insertionen und Cyclopropanierungspfade , 2012 .
[17] F. Rominger,et al. Gold vinylidene complexes: intermolecular C(sp3)-H insertions and cyclopropanations pathways. , 2012, Angewandte Chemie.
[18] S. N. Osipov,et al. Cyclobutene ring-opening of bicyclo[4.2.0]octa-1,6-dienes: access to CF3-substituted 5,6,7,8-tetrahydro-1,7-naphthyridines. , 2012, The Journal of organic chemistry.
[19] M. Ohashi,et al. Nickel-catalyzed intermolecular [2 + 2] cycloaddition of conjugated enynes with alkenes. , 2012, Journal of the American Chemical Society.
[20] H. W. Lam,et al. Rhodium-catalyzed [2 + 2] cycloaddition of ynamides with nitroalkenes. , 2012, Organic letters.
[21] 郑柯,et al. 手性氮氧-Ni(II)络合物催化三氟甲基酮酸酯的不对称羰基ene 反应 , 2012 .
[22] Lili Lin,et al. Recent progress in enantioselective synthesis of C3-functionalized oxindoles: rare earth metals take action , 2012 .
[23] Lili Lin,et al. Chiral N,N'-dioxides: new ligands and organocatalysts for catalytic asymmetric reactions. , 2011, Accounts of chemical research.
[24] A. Mezzetti,et al. Enantioselective Ficini reaction: ruthenium/PNNP-catalyzed [2+2] cycloaddition of ynamides with cyclic enones. , 2011, Angewandte Chemie.
[25] B. Alcaide,et al. Expeditious Entry to Enantiopure Mono‐ and Bis(Tricyclic) β‐Lactams by Single or Double [2+2] Cycloaddition of Allenynes , 2011 .
[26] R. Hsung,et al. Copper-catalyzed Ficini [2 + 2] cycloaddition of ynamides. , 2010, Organic letters.
[27] M. Siebert,et al. Differentiating mechanistic possibilities for the thermal, intramolecular [2 + 2] cycloaddition of allene-ynes. , 2010, Journal of the American Chemical Society.
[28] Keisuke Suzuki,et al. Siloxy(trialkoxy)ethene undergoes regioselective [2+2] cycloaddition to ynones and ynoates en route to functionalized cyclobutenediones. , 2010, Chemical communications.
[29] G. Hilt,et al. Cobalt catalysis at the crossroads: cobalt-catalyzed Alder-ene reaction versus [2 + 2] cycloaddition. , 2010, Organic letters.
[30] A. Chan,et al. Ligand-controlled enantioselective [2 + 2] cycloaddition of oxabicyclic alkenes with terminal alkynes using chiral iridium catalysts. , 2010, Organic letters.
[31] H. Saegusa,et al. Total syntheses of (+)- and (-)-pestalotiopsin A. , 2009, The Journal of organic chemistry.
[32] G. Hilt,et al. Cobalt‐katalysierte [2+2]‐Cycloaddition , 2008 .
[33] G. Hilt,et al. Cobalt-catalyzed [2+2] cycloaddition. , 2008, Angewandte Chemie.
[34] M. Fushimi,et al. Catalytic enantioselective [2 + 4] and [2 + 2] cycloaddition reactions with propiolamides. , 2008, Journal of the American Chemical Society.
[35] T. Ovaska,et al. Intramolecular thermal allenyne [2 + 2] cycloadditions; facile construction of the 5-6-4 ring core of sterpurene. , 2008, Tetrahedron letters.
[36] E. Corey,et al. Highly enantioselective [2+2]-cycloaddition reactions catalyzed by a chiral aluminum bromide complex. , 2007, Journal of the American Chemical Society.
[37] Valery M. Dembitsky,et al. Bioactive cyclobutane-containing alkaloids , 2007, Journal of Natural Medicines.
[38] Xuefeng Jiang,et al. Intramolecular [2+2]-cycloaddition of propargylic 2,3-allenoates for the efficient synthesis of 3-oxabicyclo[4.2.0]octa-1(8),5-dien-4-ones: a dramatic substituent effect , 2007 .
[39] F. Inagaki,et al. Thermal [2+2] cycloaddition of allenynes: easy construction of bicyclo[6.2.0]deca-1,8-dienes, bicyclo[5.2.0]nona-1,7-dienes, and bicyclo[4.2.0]octa-1,6-dienes. , 2007, The Journal of organic chemistry.
[40] K. Iguchi,et al. Catalytic enantioselective [2+2]-cycloaddition reaction of 2-methoxycarbonyl-2-cyclopenten-1-one by chiral copper catalyst , 2006 .
[41] T. Shibata,et al. Rh-catalyzed enantioselective [2 + 2] cycloaddition of alkynyl esters and norbornene derivatives. , 2006, Organic letters.
[42] N. Martín,et al. Thermal [2+2] intramolecular cycloadditions of fuller-1,6-enynes. , 2006, Angewandte Chemie.
[43] H. Saegusa,et al. Synthetic studies of pestalotiopsin A: asymmetric synthesis of the 2-oxabicyclo[3.2.0]heptane substructure , 2005 .
[44] H. Ohno,et al. Thermal intramolecular [2+2] cycloaddition of allenenes and allenynes: diastereoselective access to bicyclic nitrogen heterocycles. , 2005, Angewandte Chemie.
[45] N. Riddell,et al. Ruthenium-catalyzed [2 + 2] cycloadditions of ynamides. , 2005, Organic letters.
[46] K. Takasu,et al. A practical catalytic method for preparing highly substituted cyclobutanes and cyclobutenes. , 2005, Journal of the American Chemical Society.
[47] M. Koketsu,et al. Synthesis of 3-acyl-1-alkyl-2-alkylseleno-1-cyclobutene using alkyneselenolate. , 2004, The Journal of organic chemistry.
[48] S. Kozmin,et al. Silver-catalyzed [2 + 2] cycloadditions of siloxy alkynes. , 2004, Journal of the American Chemical Society.
[49] M. Snapper,et al. Ring-opening metathesis/oxy-cope rearrangement: a new strategy for the synthesis of bicyclic medium ring-containing compounds. , 2003, Journal of the American Chemical Society.
[50] E. Lee-Ruff,et al. Enantiomerically pure cyclobutane derivatives and their use in organic synthesis. , 2003, Chemical reviews.
[51] D. Kaufmann,et al. The application of cyclobutane derivatives in organic synthesis. , 2003, Chemical reviews.
[52] D. Rayabarapu,et al. Cross [2 + 2] cycloaddition of bicyclic alkenes with alkynes mediated by cobalt complexes: a facile synthesis of cyclobutene derivatives. , 2001, The Journal of organic chemistry.
[53] Chien‐Hong Cheng,et al. Nickel‐Catalyzed [2+2] Cycloaddition of Alkynes with Activated Cyclic Alkenes: Synthesis and Novel Ring Expansion Studies of Cyclobutene Products , 2000 .
[54] W. Tam,et al. Ruthenium-catalyzed [2 + 2] cycloadditions of 2-substituted norbornenes. , 2000, Organic letters.
[55] J. Springer,et al. A comprehensive study of [2 + 2] cycloadditions and ene reactions of alkynyl chromium and tungsten carbene complexes with enol ethers and ketene acetals and of the stereochemistry of the electrocyclic ring opening of cyclobutenyl carbene complexes , 1999 .
[56] M. Miesch,et al. Synthesis of the angular triquinane (±)-pentalenene via small ring intermediates. , 1992 .
[57] Y. Hayashi,et al. Asymmetric [2 + 2] cycloaddition reaction catalyzed by a chiral titanium reagent , 1989 .
[58] W. Wulff,et al. Chromium and Tungsten Pentacarbonyl Groups as Reactivity Auxiliaries in (2 + 2) Cycloadditions. , 1989 .
[59] W. Wulff,et al. The chromium and tungsten pentacarbonyl groups as reactivity auxiliaries in [2 + 2] cycloadditions , 1988 .
[60] G. Rousseau,et al. Reaction of ketenealkylsilylacetals with ethyl propiolate , 1988 .
[61] M. Rosenblum,et al. Condensation of propiolic esters with olefins catalyzed by the C5H5Fe(CO)2 cation , 1982 .
[62] B. Snider,et al. Lewis acid catalyzed reactions of acetylenic esters with alkenes. Stereochemistry and regiochemistry , 1980 .
[63] S. Sealfon,et al. Lewis acid catalyzed reactions of methyl propiolate with unactivated alkenes , 1979 .
[64] H. Hoffmann,et al. Cyclobutenecarboxylic esters via aluminum chloride induced [2 + 2] cycloadditions of 2-propynoic esters to cyclic olefins , 1979 .
[65] R. Clark,et al. [2 + 2] Cycloadditions of silyl enol ethers and dimethyl acetylenedicarboxylate, dimethyl fumarate, and methyl crotonate , 1979 .
[66] R. Clark,et al. [2 + 2] Cycloaddition of ethyl propiolate and silyl enol ethers , 1979 .
[67] R. E. Conn,et al. The lewis acid catalyzed reaction of 3-butyn-2-one with alkenes , 1977 .