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- Prolinamides containing 2-(2-aminocyclohexyl)phenols as highly enantioselective organocatalysts for aldol reactions. Tolga A. Yeşil, Taner Atalar, Mustafa Yavuz, Erkan Ertürk
, Org. Biomol. Chem.
, 2023
, 21
, 5809
- A tripeptide-like prolinamide-thiourea as an aldol reaction catalyst. Stamatis Fotaras, Christoforos G. Kokotos, George Kokotos
, Org. Biomol. Chem.
, 2012
, 10
, 5613
- Combinatorial synthesis of nicotine analogs using an Ugi 4-CR/cyclization-reduction strategy. Luis A. Polindara-García, Alfredo Vazquez
, Org. Biomol. Chem.
, 2014
, 12
, 7068
- l-Proline supported on ionic liquid-modified magnetic nanoparticles as a highly efficient and reusable organocatalyst for direct asymmetric aldol reaction in water. Yu Kong, Rong Tan, Lili Zhao, Donghong Yin
, Green Chem.
, 2013
, 15
, 2422
- Robust asymmetric synthesis of unnatural alkenyl amino acids for conformationally constrained α-helix peptides. Boris Aillard, Naomi S. Robertson, Adam R. Baldwin, Siobhan Robins, Andrew G. Jamieson
, Org. Biomol. Chem.
, 2014
, 12
, 8775
- Proline derived guanidine catalysts forge extensive H-bonded architectures: a solution and solid state study. Zahraa S. Al-Taie, Simon R. Anetts, Jeppe Christensen, Simon J. Coles, Peter N. Horton, Daniel M. Evans, Leigh F. Jones, Frank F. J. de Kleijne, Shaun M. Ledbetter, Yassin T. H. Mehdar, Patrick J. Murphy, Jack A. Wilson
, RSC Adv.
, 2020
, 10
, 22397
- Synergistic effects within a C
2-symmetric organocatalyst: the potential formation of a chiral catalytic pocket. Joshua P. Delaney, Hannah L. Brozinski, Luke C. Henderson
, Org. Biomol. Chem.
, 2013
, 11
, 2951
- Recyclable organocatalysts based on hybrid silicas. M. Ferré, R. Pleixats, M. Wong Chi Man, X. Cattoën
, Green Chem.
, 2016
, 18
, 881
- Enantioselective synthesis of α-perfluoroalkylated prolines, their 6,7-membered homologues and derivatives. Natalia G. Voznesenskaia, Olga I. Shmatova, Victor N. Khrustalev, Valentine G. Nenajdenko
, Org. Biomol. Chem.
, 2018
, 16
, 7004
- Rapid and efficient syntheses of tryptophans using a continuous-flow quaternization–substitution reaction of gramines with a chiral nucleophilic glycine equivalent. Daichi Koiwa, Masayuki Ohira, Takahiro Hiramatsu, Hidenori Abe, Tetsuji Kawamoto, Yuji Ishihara, Bernardo Ignacio, Noel Mansour, Todd Romoff
, Org. Biomol. Chem.
, 2022
, 20
, 8331