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- Stereoselective synthesis of oxazolidinonyl-fused piperidines of interest as selective muscarinic (M1) receptor agonists: a novel M1 allosteric modulator. Kenneth J. Broadley, Maxime G. P. Buffat, Erica Burnell, Robin H. Davies, Xavier Moreau, Stephen Snee, Eric J. Thomas
, Org. Biomol. Chem.
, 2016
, 14
, 2057
- Highly effective and recyclable chiral auxiliaries: a study of the synthesis and use of three 4-isopropyl-5,5-diaryloxazolidin-2-ones. Karen Alexander (née Gillon), Stuart Cook, Colin L. Gibson, Alan R. Kennedy
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 1538
- Regioselectivity of the trifluoroethanol-promoted intramolecular N-Boc–epoxide cyclization towards 1,3-oxazolidin-2-ones and 1,3-oxazinan-2-ones. Hemi Borgohain, Kangkan Talukdar, Bipul Sarma, Sajal Kumar Das
, Org. Biomol. Chem.
, 2020
, 18
, 7401
- Enantioselective synthesis of 2-substituted 3-aminopropanoic acid (β-alanine) derivatives which are β-analogues of aromatic amino acids. Elena Arvanitis, Holger Ernst, Alice A. LudwigéD’Souza, Andrew J. Robinson, Peter B. Wyatt
, J. Chem. Soc., Perkin Trans. 1
, 1998
, 521
- Reactions of secondary propargylamines with heteroallenes for the synthesis of diverse heterocycles. Vsevolod A. Peshkov, Olga P. Pereshivko, Anton A. Nechaev, Anatoly A. Peshkov, Erik V. Van der Eycken
, Chem. Soc. Rev.
, 2018
, 47
, 3861
- Carbon dioxide utilization with C–N bond formation: carbon dioxide capture and subsequent conversion. Zhen-Zhen Yang, Liang-Nian He, Jiao Gao, An-Hua Liu, Bing Yu
, Energy Environ. Sci.
, 2012
, 5
, 6602
- Stereoselective synthesis of (E)-trisubstituted α,β-unsaturated amides and acids. Fred J. P. Feuillet, Matt Cheeseman, Mary F. Mahon, Steven D. Bull
, Org. Biomol. Chem.
, 2005
, 3
, 2976
- Potassium trimethylsilanolate induced cleavage of 1,3-oxazolidin-2- and 5-ones, and application to the synthesis of (R)-salmeterol. Diane M. Coe, Rossana Perciaccante, Panayiotis A. Procopiou
, Org. Biomol. Chem.
, 2003
, 1
, 1106
- Regio- and stereoselective ring-opening of chiral 1,3-oxazolidin-2-one derivatives by organocopper reagents provides novel access to di-, tri- and tetra-substituted alkene
dipeptide isosteres
. Shinya Oishi, Ayumu Niida, Takae Kamano, Yoshihisa Miwa, Tooru Taga, Yoshihiko Odagaki, Nobuyuki Hamanaka, Mikio Yamamoto, Keiichi Ajito, Hirokazu Tamamura, Akira Otaka, Nobutaka Fujii
, J. Chem. Soc., Perkin Trans. 1
, 2002
, 1786
- Enantioselective synthesis of 2-substituted 4-aminobutanoic acid (GABA) analogues via cyanomethylation of chiral enolates. Shamim Azam, Alice A. D'Souza, Peter B. Wyatt
, J. Chem. Soc., Perkin Trans. 1
, 1996
, 621