These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
191 related articles for article (PubMed ID: 23153274)
1. Expanding the scope of donor/acceptor carbenes to N-phthalimido donor groups: diastereoselective synthesis of 1-cyclopropane α-amino acids. Alford JS; Davies HM Org Lett; 2012 Dec; 14(23):6020-3. PubMed ID: 23153274 [TBL] [Abstract][Full Text] [Related]
2. Expedient synthesis of cyclopropane alpha-amino acids by the catalytic asymmetric cyclopropanation of alkenes using iodonium ylides derived from methyl nitroacetate. Moreau B; Charette AB J Am Chem Soc; 2005 Dec; 127(51):18014-5. PubMed ID: 16366547 [TBL] [Abstract][Full Text] [Related]
3. Synthesis of donor-acceptor alkynylcyclopropanes by diastereoselective cyclopropanation of electron-deficient alkenes with alkoxyalkynyl Fischer carbene complexes. Barluenga J; Fernández-Rodríguez MA; García-García P; Aguilar E; Merino I Chemistry; 2005 Dec; 12(1):303-13. PubMed ID: 16294347 [TBL] [Abstract][Full Text] [Related]
4. Gold(I)-catalyzed intermolecular cyclopropanation of enynes with alkenes: trapping of two different gold carbenes. López S; Herrero-Gómez E; Pérez-Galán P; Nieto-Oberhuber C; Echavarren AM Angew Chem Int Ed Engl; 2006 Sep; 45(36):6029-32. PubMed ID: 16900550 [No Abstract] [Full Text] [Related]
5. Experimental evidence for the all-up reactive conformation of chiral rhodium(II) carboxylate catalysts: enantioselective synthesis of cis-cyclopropane alpha-amino acids. Lindsay VN; Lin W; Charette AB J Am Chem Soc; 2009 Nov; 131(45):16383-5. PubMed ID: 19860407 [TBL] [Abstract][Full Text] [Related]
6. Diastereoselective synthesis of cyclopropane amino acids using diazo compounds generated in situ. Adams LA; Aggarwal VK; Bonnert RV; Bressel B; Cox RJ; Shepherd J; de Vicente J; Walter M; Whittingham WG; Winn CL J Org Chem; 2003 Nov; 68(24):9433-40. PubMed ID: 14629169 [TBL] [Abstract][Full Text] [Related]
7. Theoretical study on the mechanism of the [2+1] thermal cycloaddition between alkenes and stable singlet (phosphino)(silyl)carbenes. Lecea B; Ayerbe M; Arrieta A; Cossío FP; Branchadell V; Ortuño RM; Baceiredo A J Org Chem; 2007 Jan; 72(2):357-66. PubMed ID: 17221950 [TBL] [Abstract][Full Text] [Related]
10. Preparation of enolate-homoenolate species as (Z)-gamma-siloxyallylmetal equivalents: sequential 1,4-addition of bis(iodozincio)methane to 1,4-dicarbonylbutenes and cyclopropanation. Hirayama T; Oshima K; Matsubara S Angew Chem Int Ed Engl; 2005 May; 44(21):3293-6. PubMed ID: 15844119 [No Abstract] [Full Text] [Related]
16. Transition-Metal-Free Cyclopropanation of 2-Aminoacrylates with N-Tosylhydrazones: A General Route to Cyclopropane α-Amino Acid with Contiguous Quaternary Carbon Centers. Zhu C; Li J; Chen P; Wu W; Ren Y; Jiang H Org Lett; 2016 Mar; 18(6):1470-3. PubMed ID: 26958741 [TBL] [Abstract][Full Text] [Related]
17. An expedient and practical method for the synthesis of a diverse series of cyclopropane alpha-amino acids and amines. Wurz RP; Charette AB J Org Chem; 2004 Feb; 69(4):1262-9. PubMed ID: 14961679 [TBL] [Abstract][Full Text] [Related]
18. Highly enantioselective synthesis of α-amino acid derivatives by an NHC-catalyzed intermolecular Stetter reaction. Jousseaume T; Wurz NE; Glorius F Angew Chem Int Ed Engl; 2011 Feb; 50(6):1410-4. PubMed ID: 21290524 [No Abstract] [Full Text] [Related]
19. A straightforward and highly diastereoselective access to functionalized monofluorinated cyclopropanes via a Michael initiated ring closure reaction. Ferrary T; David E; Milanole G; Besset T; Jubault P; Pannecoucke X Org Lett; 2013 Nov; 15(21):5598-601. PubMed ID: 24138105 [TBL] [Abstract][Full Text] [Related]
20. Side-arm-promoted highly enantioselective ring-opening reactions and kinetic resolution of donor-acceptor cyclopropanes with amines. Zhou YY; Wang LJ; Li J; Sun XL; Tang Y J Am Chem Soc; 2012 Jun; 134(22):9066-9. PubMed ID: 22578301 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]