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Quantum-chemical predictions of redox potentials of carbamates in methanol Luisa Haya, Francisco J. Sayago, Ana M. Mainar, Carlos Cativiela, José S. Urieta
, Phys. Chem. Chem. Phys.
, 2011
, 13
, 17696 Total synthesis of phenanthroindolizidine alkaloids via asymmetric deprotonation of N -Boc-pyrrolidine Meng Deng, Bo Su, Hui Zhang, Yuxiu Liu, Qingmin Wang
, RSC Adv.
, 2014
, 4
, 14979 On the synthesis of α-amino sulfoxides Peter J. Rayner, Giacomo Gelardi, Peter O'Brien, Richard A. J. Horan, David C. Blakemore
, Org. Biomol. Chem.
, 2014
, 12
, 3499 Ambient temperature zincation of
N -Boc pyrrolidine and its solvent dependency Jennifer A. Garden, Alan R. Kennedy, Robert E. Mulvey, Stuart D. Robertson
, Chem. Commun.
, 2012
, 48
, 5265 Reactivity series for
s -BuLi /diamine -mediated lithiation of
N -Boc pyrrolidine : applications in catalysis and lithiation of N -Boc piperidine Matthew J. McGrath, Julia L. Bilke, Peter O'Brien
, Chem. Commun.
, 2006
, 2607 Recent advances in visible light-activated radical coupling reactions triggered by (i) ruthenium, (ii) iridium and (iii) organic photoredox agents Jonathan D. Bell, John A. Murphy
, Chem. Soc. Rev.
, 2021
, 50
, 9540 Synthesis of sparteine-like chiral diamines and evaluation in the enantioselective lithiation–substitution of N -(tert -butoxycarbonyl)pyrrolidine Jean-Paul R. Hermet, David W. Porter, Michael J. Dearden, Justin R. Harrison, Tobias Koplin, Peter O'Brien, Jérôme Parmene, Vladimir Tyurin, Adrian C. Whitwood, John Gilday, Neil M. Smith
, Org. Biomol. Chem.
, 2003
, 1
, 3977 Mechanistic interrogation of the asymmetric lithiation-trapping of N -thiopivaloyl azetidine and pyrrolidine Peter J. Rayner, Joshua C. Smith, Charline Denneval, Peter O'Brien, Paul A. Clarke, Richard A. J. Horan
, Chem. Commun.
, 2016
, 52
, 1354 Basic instinct: design, synthesis and evaluation of (+)-sparteine surrogates for asymmetric synthesis Peter O'Brien
, Chem. Commun.
, 2008
, 655 Diamidophosphites from β-hydroxyamides: readily assembled ligands for Pd-catalyzed asymmetric allylic substitution Ilya V. Chuchelkin, Konstantin N. Gavrilov, Nataliya E. Borisova, Alexander M. Perepukhov, Alexander V. Maximychev, Sergey V. Zheglov, Vladislav K. Gavrilov, Ilya D. Firsin, Vladislav S. Zimarev, Igor S. Mikhel, Victor A. Tafeenko, Elena V. Murashova, Vladimir V. Chernyshev, Nataliya S. Goulioukina
, Dalton Trans.
, 2020
, 49
, 5625