Artículos de revistas sobre el tema "Α-diazocarbonyl compounds"
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Krasavin, Mikhail, Maria Eremeyeva, Daniil Zhukovsky y Dmitry Dar’in. "The Use of α-Diazo-γ-butyrolactams in the Büchner–Curtius–Schlotterbeck Reaction of Cyclic Ketones Opens New Entry to Spirocyclic Pyrrolidones". Synlett 31, n.º 10 (23 de marzo de 2020): 982–86. http://dx.doi.org/10.1055/s-0040-1708011.
Texto completoWang, Zikun, Xihe Bi, Yongjiu Liang, Peiqiu Liao y Dewen Dong. "A copper-catalyzed formal O–H insertion reaction of α-diazo-1,3-dicarbonyl compounds to carboxylic acids with the assistance of isocyanide". Chem. Commun. 50, n.º 30 (2014): 3976–78. http://dx.doi.org/10.1039/c4cc00402g.
Texto completoDong, Shunxi, Xiaohua Liu y Xiaoming Feng. "Asymmetric Catalytic Rearrangements with α-Diazocarbonyl Compounds". Accounts of Chemical Research 55, n.º 3 (14 de enero de 2022): 415–28. http://dx.doi.org/10.1021/acs.accounts.1c00664.
Texto completoFord, Alan, Hugues Miel, Aoife Ring, Catherine N. Slattery, Anita R. Maguire y M. Anthony McKervey. "Modern Organic Synthesis with α-Diazocarbonyl Compounds". Chemical Reviews 115, n.º 18 (18 de agosto de 2015): 9981–10080. http://dx.doi.org/10.1021/acs.chemrev.5b00121.
Texto completoLübcke, Marvin, Dina Bezhan y Kálmán J. Szabó. "Trifluoromethylthiolation–arylation of diazocarbonyl compounds by modified Hooz multicomponent coupling". Chemical Science 10, n.º 23 (2019): 5990–95. http://dx.doi.org/10.1039/c9sc00829b.
Texto completoChen, Xun, Ying Xie, Xinsheng Xiao, Guoqiang Li, Yuanfu Deng, Huanfeng Jiang y Wei Zeng. "Rh(iii)-catalyzed chelation-assisted intermolecular carbenoid functionalization of α-imino Csp3–H bonds". Chemical Communications 51, n.º 83 (2015): 15328–31. http://dx.doi.org/10.1039/c5cc06428g.
Texto completoLiu, Lu y Junliang Zhang. "Gold-catalyzed transformations of α-diazocarbonyl compounds: selectivity and diversity". Chemical Society Reviews 45, n.º 3 (2016): 506–16. http://dx.doi.org/10.1039/c5cs00821b.
Texto completoWang, Kang, Shufeng Chen, Hang Zhang, Shuai Xu, Fei Ye, Yan Zhang y Jianbo Wang. "Pd(0)-catalyzed cross-coupling of allyl halides with α-diazocarbonyl compounds or N-mesylhydrazones: synthesis of 1,3-diene compounds". Organic & Biomolecular Chemistry 14, n.º 15 (2016): 3809–20. http://dx.doi.org/10.1039/c6ob00454g.
Texto completoCortés González, Miguel A., Xingguo Jiang, Patrik Nordeman, Gunnar Antoni y Kálmán J. Szabó. "Rhodium-mediated 18F-oxyfluorination of diazoketones using a fluorine-18-containing hypervalent iodine reagent". Chemical Communications 55, n.º 89 (2019): 13358–61. http://dx.doi.org/10.1039/c9cc06905d.
Texto completoGhorai, Jayanta, Manthena Chaitanya y Pazhamalai Anbarasan. "Cp*Co(iii)-catalysed selective alkylation of C–H bonds of arenes and heteroarenes with α-diazocarbonyl compounds". Organic & Biomolecular Chemistry 16, n.º 40 (2018): 7346–50. http://dx.doi.org/10.1039/c8ob02111b.
Texto completoYE, T. y M. A. MCKERVEY. "ChemInform Abstract: Organic Synthesis with α-Diazocarbonyl Compounds". ChemInform 25, n.º 39 (18 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199439313.
Texto completoYE, T. y M. A. MCKERVEY. "ChemInform Abstract: Organic Synthesis with α-Diazocarbonyl Compounds". ChemInform 25, n.º 44 (18 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199444267.
Texto completoKIM, S. y J. R. CHO. "ChemInform Abstract: Radical Cyclization of α-Diazocarbonyl Compounds." ChemInform 25, n.º 21 (19 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199421077.
Texto completoZhang, He, Tongxiang Cao, Hejiang Luo, Lianfen Chen y Shifa Zhu. "Enynone-enabled migratory insertion and Schmittel cyclization cascade for the synthesis of furan-fused fluorenes". Organic Chemistry Frontiers 6, n.º 8 (2019): 1118–22. http://dx.doi.org/10.1039/c9qo00045c.
Texto completoHou, Wei, Yaxi Yang, Yunxiang Wu, Huijin Feng, Yuanchao Li y Bing Zhou. "Rhodium(iii)-catalyzed alkylation of primary C(sp3)–H bonds with α-diazocarbonyl compounds". Chemical Communications 52, n.º 62 (2016): 9672–75. http://dx.doi.org/10.1039/c6cc03846h.
Texto completoGeigle, Stefanie N., Laura A. Wyss, Shana J. Sturla y Dennis G. Gillingham. "Copper carbenes alkylate guanine chemoselectively through a substrate directed reaction". Chemical Science 8, n.º 1 (2017): 499–506. http://dx.doi.org/10.1039/c6sc03502g.
Texto completoYu, Sifan, Jinzhou Chen, Gengxin Liu, Jinping Lei, Wenhao Hu y Huang Qiu. "A gold(i)-catalysed chemoselective three-component reaction between phenols, α-diazocarbonyl compounds and allenamides". Chemical Communications 56, n.º 11 (2020): 1649–52. http://dx.doi.org/10.1039/c9cc09470a.
Texto completoZhou, Minghui, Qin Su, Yesu Addepalli, Yun He y Zhen Wang. "An asymmetric Mannich reaction of α-diazocarbonyl compounds and N-sulfonyl cyclic ketimines catalyzed by complexes generated from chiral and achiral phosphines with gold(i)". Organic & Biomolecular Chemistry 16, n.º 16 (2018): 2923–31. http://dx.doi.org/10.1039/c8ob00577j.
Texto completoChuprun, Sergey, Dmitry Dar’in, Grigory Kantin y Mikhail Krasavin. "[3+2]-Cycloaddition of α-Diazocarbonyl Compounds with Arenediazonium Salts Catalyzed by Silver Nitrate Delivers 2,5-Disubstituted Tetrazoles". Synthesis 51, n.º 21 (12 de agosto de 2019): 3998–4005. http://dx.doi.org/10.1055/s-0039-1690159.
Texto completoRao, Changqing, Shaoyu Mai y Qiuling Song. "Rh(ii)/phosphine-cocatalyzed synthesis of dithioketal derivatives from diazo compounds through simultaneous construction of two different C–S bonds". Chemical Communications 54, n.º 47 (2018): 5964–67. http://dx.doi.org/10.1039/c8cc01656a.
Texto completoAher, Yogesh N., Dhanaji M. Lade y Amit B. Pawar. "Cp*Ir(iii)-catalyzed C–H/N–H functionalization of sulfoximines for the synthesis of 1,2-benzothiazines at room temperature". Chemical Communications 54, n.º 49 (2018): 6288–91. http://dx.doi.org/10.1039/c8cc03288b.
Texto completoKidonakis, Marios y Manolis Stratakis. "Reduction of the Diazo Functionality of α-Diazocarbonyl Compounds into a Methylene Group by NH3BH3 or NaBH4 Catalyzed by Au Nanoparticles". Nanomaterials 11, n.º 1 (18 de enero de 2021): 248. http://dx.doi.org/10.3390/nano11010248.
Texto completoPeng, Cheng, Wei Zhang, Guobing Yan y Jianbo Wang. "Arylation and Vinylation of α-Diazocarbonyl Compounds with Boroxines". Organic Letters 11, n.º 7 (2 de abril de 2009): 1667–70. http://dx.doi.org/10.1021/ol900362d.
Texto completoZhang, Zhenhua y Jianbo Wang. "Recent studies on the reactions of α-diazocarbonyl compounds". Tetrahedron 64, n.º 28 (julio de 2008): 6577–605. http://dx.doi.org/10.1016/j.tet.2008.04.074.
Texto completoElkin, Pavel K., Vitalij V. Levin, Alexander D. Dilman, Marina I. Struchkova, Pavel A. Belyakov, Dmitry E. Arkhipov, Alexander A. Korlyukov y Vladimir A. Tartakovsky. "Reactions of CF3-substituted boranes with α-diazocarbonyl compounds". Tetrahedron Letters 52, n.º 41 (octubre de 2011): 5259–63. http://dx.doi.org/10.1016/j.tetlet.2011.07.141.
Texto completoRao, M. V. Krishna, K. Nagarjuna Reddy, B. Sridhar y B. V. Subba Reddy. "ortho-Alkylation of 2-arylindazoles with α-diazocarbonyl compounds". Tetrahedron Letters 61, n.º 35 (agosto de 2020): 152252. http://dx.doi.org/10.1016/j.tetlet.2020.152252.
Texto completoSolovyev, Igor V., Daniil D. Zhukovsky, Dmitry V. Dar’in y Mikhail Yu Krasavin. "N-Alkylation of Nitrogen Heterocycles with α-Diazocarbonyl Compounds". Chemistry of Heterocyclic Compounds 56, n.º 7 (julio de 2020): 809–13. http://dx.doi.org/10.1007/s10593-020-02736-y.
Texto completoFord, Alan, Hugues Miel, Aoife Ring, Catherine N. Slattery, Anita R. Maguire y M. Anthony McKervey. "ChemInform Abstract: Modern Organic Synthesis with α-Diazocarbonyl Compounds". ChemInform 46, n.º 46 (27 de octubre de 2015): no. http://dx.doi.org/10.1002/chin.201546271.
Texto completoRamakrishna, D. S. "Preparation of Novel Chiral α-Diazocarbonyl Compounds Using Regitz’s Methodology". Organic Preparations and Procedures International 54, n.º 2 (7 de enero de 2022): 178–83. http://dx.doi.org/10.1080/00304948.2021.2010466.
Texto completoFeng, Jiajun, Xiangyan Yi, Yaofeng Fu, Yang Yu y Fei Huang. "Progress in N-H Insertion Reaction of α-Diazocarbonyl Compounds". Chinese Journal of Organic Chemistry 39, n.º 11 (2019): 3013. http://dx.doi.org/10.6023/cjoc201904044.
Texto completoZhang, Yan y Jianbo Wang. "Recent development of reactions with α-diazocarbonyl compounds as nucleophiles". Chemical Communications, n.º 36 (2009): 5350. http://dx.doi.org/10.1039/b908378b.
Texto completoSlattery, Catherine N., Alan Ford y Anita R. Maguire. "Catalytic asymmetric C–H insertion reactions of α-diazocarbonyl compounds". Tetrahedron 66, n.º 34 (agosto de 2010): 6681–705. http://dx.doi.org/10.1016/j.tet.2010.05.073.
Texto completoChen, Shufeng y Jianbo Wang. "Palladium-catalyzed reaction of allyl halides with α-diazocarbonyl compounds". Chemical Communications, n.º 35 (2008): 4198. http://dx.doi.org/10.1039/b806970k.
Texto completoPeng, Cheng, Yan Wang y Jianbo Wang. "Palladium-Catalyzed Cross-Coupling of α-Diazocarbonyl Compounds with Arylboronic Acids". Journal of the American Chemical Society 130, n.º 5 (febrero de 2008): 1566–67. http://dx.doi.org/10.1021/ja0782293.
Texto completoKoduri, Naga D., Zhiguo Wang, Garrett Cannell, Kate Cooley, Tsebaot Mesfin Lemma, Kun Miao, Michael Nguyen et al. "Enaminones via Ruthenium-Catalyzed Coupling of Thioamides and α-Diazocarbonyl Compounds". Journal of Organic Chemistry 79, n.º 16 (31 de julio de 2014): 7405–14. http://dx.doi.org/10.1021/jo5011312.
Texto completoElkin, Pavel K., Vitalij V. Levin, Alexander D. Dilman, Marina I. Struchkova, Pavel A. Belyakov, Dmitry E. Arkhipov, Alexander A. Korlyukov y Vladimir A. Tartakovsky. "ChemInform Abstract: Reactions of CF3-Substituted Boranes with α-Diazocarbonyl Compounds." ChemInform 43, n.º 4 (29 de diciembre de 2011): no. http://dx.doi.org/10.1002/chin.201204156.
Texto completoPopik, Vladimir V. "The role of molecular geometry in the Wolff rearrangement of α-diazocarbonyl compounds Conformational control or structural constraints?" Canadian Journal of Chemistry 83, n.º 9 (1 de septiembre de 2005): 1382–90. http://dx.doi.org/10.1139/v05-152.
Texto completoSemenov, S. G. y M. V. Makarova. "Quantum chemical study of α-diazocarbonyl bullvalene derivatives and related heterocyclic compounds". Russian Journal of Organic Chemistry 50, n.º 3 (marzo de 2014): 439–41. http://dx.doi.org/10.1134/s1070428014030245.
Texto completoSengupta, Saumitra y Somnath Mondal. "InCl3: A new Lewis acid catalyst for reactions with α-diazocarbonyl compounds". Tetrahedron Letters 40, n.º 49 (diciembre de 1999): 8685–88. http://dx.doi.org/10.1016/s0040-4039(99)01843-2.
Texto completoKidonakis, Marios y Manolis Stratakis. "Au Nanoparticle-Catalyzed Insertion of Carbenes from α-Diazocarbonyl Compounds into Hydrosilanes". Organic Letters 20, n.º 13 (27 de junio de 2018): 4086–89. http://dx.doi.org/10.1021/acs.orglett.8b01638.
Texto completoAusteri, Martina, Diane Rix, Walid Zeghida y Jérôme Lacour. "CpRu-Catalyzed O−H Insertion and Condensation Reactions of α-Diazocarbonyl Compounds". Organic Letters 13, n.º 6 (18 de marzo de 2011): 1394–97. http://dx.doi.org/10.1021/ol2000815.
Texto completoYang, Xiaobo, Jiyang Jie, Haoyi Li y Meihui Piao. "Ir(iii)-catalyzed synthesis of isoquinolines from benzimidates and α-diazocarbonyl compounds". RSC Advances 6, n.º 62 (2016): 57371–74. http://dx.doi.org/10.1039/c6ra10045g.
Texto completoLiu, Lu y Junliang Zhang. "ChemInform Abstract: Gold-Catalyzed Transformations of α-Diazocarbonyl Compounds: Selectivity and Diversity". ChemInform 47, n.º 13 (marzo de 2016): no. http://dx.doi.org/10.1002/chin.201613252.
Texto completoSlattery, Catherine N., Alan Ford y Anita R. Maguire. "ChemInform Abstract: Catalytic Asymmetric C-H Insertion Reactions of α-Diazocarbonyl Compounds". ChemInform 41, n.º 48 (4 de noviembre de 2010): no. http://dx.doi.org/10.1002/chin.201048241.
Texto completoAlavi, Sima, Jian-Bin Lin y Huck K. Grover. "Copper-Catalyzed Annulation of Indolyl α-Diazocarbonyl Compounds Leads to Structurally Rearranged Carbazoles". Organic Letters 23, n.º 14 (1 de julio de 2021): 5559–64. http://dx.doi.org/10.1021/acs.orglett.1c01965.
Texto completoJabre, Nitinkumar D. y Matthias Brewer. "Stereoelectronic Effects in the Fragmentation of γ-Silyloxy-β-hydroxy-α-diazocarbonyl Compounds". Journal of Organic Chemistry 77, n.º 21 (15 de octubre de 2012): 9910–14. http://dx.doi.org/10.1021/jo301944t.
Texto completoXu, Feng, Shiwei Zhang, Xiangnan Wu, Yu Liu, Weifeng Shi y Jianbo Wang. "2,3-Migration in Rh(II)-Catalyzed Reactions of β-Trifluoroacetamido α-Diazocarbonyl Compounds". Organic Letters 8, n.º 15 (julio de 2006): 3207–10. http://dx.doi.org/10.1021/ol061047d.
Texto completoHussaini, Syed R. y et al et al. "ChemInform Abstract: Enaminones via Ruthenium-Catalyzed Coupling of Thioamides and α-Diazocarbonyl Compounds." ChemInform 46, n.º 7 (29 de enero de 2015): no. http://dx.doi.org/10.1002/chin.201507065.
Texto completoHuang, Junmin, Xinwei Hu, Fengjuan Chen, Jiao Gui y Wei Zeng. "Rhodium(i)-catalyzed vinylation/[2 + 1] carbocyclization of 1,6-enynes with α-diazocarbonyl compounds". Organic & Biomolecular Chemistry 17, n.º 29 (2019): 7042–54. http://dx.doi.org/10.1039/c9ob01028a.
Texto completoWest, F. G., Kevin W. Glaeske y B. N. Naidu. "One-Step Synthesis of Tertiary α-Amino Ketones and α-Amino Esters From Amines and Diazocarbonyl Compounds". Synthesis 1993, n.º 10 (1993): 977–80. http://dx.doi.org/10.1055/s-1993-25984.
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