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- Transition-metal-catalyzed one-pot selenylation of electrophilic arylating agents using triphenyltin chloride/Se as a phenylselenating agent. Zeinab Shirvandi, Bahareh Atashkar, Mohammad Ali Zolfigol, Amin Rostami
, Org. Biomol. Chem.
, 2022
, 20
, 4625
- Linear free energy relationships in halogen bonds. Ibon Alkorta, Goar Sánchez-Sanz, José Elguero
, CrystEngComm
, 2013
, 15
, 3178
- Evidence for Suzuki–Miyaura cross-couplings catalyzed by ligated Pd3-clusters: from cradle to grave. Neda Jeddi, Neil W. J. Scott, Theo Tanner, Simon K. Beaumont, Ian J. S. Fairlamb
, Chem. Sci.
, 2024
, 15
, 2763
- Starburst dendrimers consisting of triphenylamine core and 9-phenylcarbazole-based dendrons: synthesis and properties. Jia You, Guiyang Li, Zhonggang Wang
, Org. Biomol. Chem.
, 2012
, 10
, 9481
- Palladium-mediated borylation of pentafluorosulfanyl functionalized compounds: the crucial role of metal fluorido complexes. Claudia Berg, Thomas Braun, Reik Laubenstein, Beatrice Braun
, Chem. Commun.
, 2016
, 52
, 3931
- Mechanistic views and computational studies on transition-metal-catalyzed reductive coupling reactions. Abing Duan, Fengjiao Xiao, Yu Lan, Linbin Niu
, Chem. Soc. Rev.
, 2022
, 51
, 9986
- Aggregates of the pentacenequinone derivative as reactors for the preparation of Ag@Cu2O core–shell NPs: an active photocatalyst for Suzuki and Suzuki type coupling reactions. Kamaldeep Sharma, Manoj Kumar, Vandana Bhalla
, Chem. Commun.
, 2015
, 51
, 12529
- Magnetic silica supported copper: a modular approach to aqueous Ullmann-type amination of aryl halides. R. B. Nasir Baig, Rajender S. Varma
, RSC Adv.
, 2014
, 4
, 6568
- Application of a low power/reduced pressure helium ICP ionization source for mass spectrometric detection of organobromine compounds and derivatized organotin compounds. Joseph W. Waggoner, Lisa S. Milstein, Mikhail Belkin, Karen L. Sutton, Joseph A. Caruso, Harry B. Fannin
, J. Anal. At. Spectrom.
, 2000
, 15
, 13
- XLVI.—Conversion of amino-acids into tertiary amino-alcohols. Alex. McKenzie, George Ogilvie Wills
, J. Chem. Soc., Trans.
, 1925
, 127
, 283