221 related articles for article (PubMed ID: 26511715)
1. Synthesis of Chiral Tertiary Alcohols by Cu(I) -Catalyzed Enantioselective Addition of Organomagnesium Reagents to Ketones.
Rong J; Pellegrini T; Harutyunyan SR
Chemistry; 2016 Mar; 22(11):3558-70. PubMed ID: 26511715
[TBL] [Abstract][Full Text] [Related]
2. Catalytic asymmetric alkylation of ketones using organometallic reagents.
Madduri AV; Harutyunyan SR; Minnaard AJ
Drug Discov Today Technol; 2013; 10(1):e21-7. PubMed ID: 24050226
[TBL] [Abstract][Full Text] [Related]
3. Synthesis of W-Phos Ligand and Its Application in the Copper-Catalyzed Enantioselective Addition of Linear Grignard Reagents to Ketones.
Luo W; Zhang LM; Zhang ZM; Zhang J
Angew Chem Int Ed Engl; 2022 Jul; 61(29):e202204443. PubMed ID: 35555954
[TBL] [Abstract][Full Text] [Related]
4. Copper(I) catalyzed asymmetric 1,2-addition of Grignard reagents to α-methyl substituted α,β-unsaturated ketones.
Madduri AV; Minnaard AJ; Harutyunyan SR
Chem Commun (Camb); 2012 Feb; 48(10):1478-80. PubMed ID: 22124420
[TBL] [Abstract][Full Text] [Related]
5. Copper-Catalyzed Enantioselective Alkylation of Enolizable Ketimines with Organomagnesium Reagents.
Ortiz P; Collados JF; Jumde RP; Otten E; Harutyunyan SR
Angew Chem Int Ed Engl; 2017 Mar; 56(11):3041-3044. PubMed ID: 28156047
[TBL] [Abstract][Full Text] [Related]
6. Access to chiral α-bromo and α-H-substituted tertiary allylic alcohols via copper(I) catalyzed 1,2-addition of Grignard reagents to enones.
Madduri AV; Minnaard AJ; Harutyunyan SR
Org Biomol Chem; 2012 Apr; 10(14):2878-84. PubMed ID: 22389187
[TBL] [Abstract][Full Text] [Related]
7. Asymmetric addition of Grignard reagents to ketones: culmination of the ligand-mediated methodology allows modular construction of chiral tertiary alcohols.
Monasterolo C; O'Gara R; Kavanagh SE; Byrne SE; Bieszczad B; Murray O; Wiesinger M; Lynch RA; Nikitin K; Gilheany DG
Chem Sci; 2022 Jun; 13(21):6262-6269. PubMed ID: 35733895
[TBL] [Abstract][Full Text] [Related]
8. Asymmetric Grignard Synthesis of Tertiary Alcohols through Rational Ligand Design.
Bieszczad B; Gilheany DG
Angew Chem Int Ed Engl; 2017 Apr; 56(15):4272-4276. PubMed ID: 28319305
[TBL] [Abstract][Full Text] [Related]
9. Catalytic asymmetric alkylation of acylsilanes.
Rong J; Oost R; Desmarchelier A; Minnaard AJ; Harutyunyan SR
Angew Chem Int Ed Engl; 2015 Mar; 54(10):3038-42. PubMed ID: 25403641
[TBL] [Abstract][Full Text] [Related]
10. 2-Azadienes as Reagents for Preparing Chiral Amines: Synthesis of 1,2-Amino Tertiary Alcohols by Cu-Catalyzed Enantioselective Reductive Couplings with Ketones.
Li K; Shao X; Tseng L; Malcolmson SJ
J Am Chem Soc; 2018 Jan; 140(2):598-601. PubMed ID: 29272124
[TBL] [Abstract][Full Text] [Related]
11. Highly enantioselective phase-transfer-catalyzed alkylation of protected alpha-amino acid amides toward practical asymmetric synthesis of vicinal diamines, alpha-amino ketones, and alpha-amino alcohols.
Ooi T; Takeuchi M; Kato D; Uematsu Y; Tayama E; Sakai D; Maruoka K
J Am Chem Soc; 2005 Apr; 127(14):5073-83. PubMed ID: 15810842
[TBL] [Abstract][Full Text] [Related]
12. Highly enantioselective Cu(I)-Tol-BINAP-catalyzed asymmetric conjugate addition of Grignard reagents to α,β-unsaturated esters.
Wang SY; Loh TP
Chem Commun (Camb); 2010 Dec; 46(46):8694-703. PubMed ID: 21038042
[TBL] [Abstract][Full Text] [Related]
13. Catalytic enantioselective conjugate addition with Grignard reagents.
López F; Minnaard AJ; Feringa BL
Acc Chem Res; 2007 Mar; 40(3):179-88. PubMed ID: 17370989
[TBL] [Abstract][Full Text] [Related]
14. Zinc(II)-catalyzed addition of Grignard reagents to ketones.
Hatano M; Ito O; Suzuki S; Ishihara K
J Org Chem; 2010 Aug; 75(15):5008-16. PubMed ID: 20560525
[TBL] [Abstract][Full Text] [Related]
15. Catalytic highly enantioselective alkylation of aldehydes with deactivated grignard reagents and synthesis of bioactive intermediate secondary arylpropanols.
Liu Y; Da CS; Yu SL; Yin XG; Wang JR; Fan XY; Li WP; Wang R
J Org Chem; 2010 Oct; 75(20):6869-78. PubMed ID: 20836546
[TBL] [Abstract][Full Text] [Related]
16. Catalytic enantioselective addition of terminal 1,3-diynes to aromatic ketones: facile access to chiral nonracemic tertiary alcohols.
Liu TL; Ma H; Zhang FG; Zheng Y; Nie J; Ma JA
Chem Commun (Camb); 2011 Dec; 47(48):12873-5. PubMed ID: 22068909
[TBL] [Abstract][Full Text] [Related]
17. A practical method for enantioselective synthesis of all-carbon quaternary stereogenic centers through NHC-Cu-catalyzed conjugate additions of alkyl- and arylzinc reagents to beta-substituted cyclic enones.
Lee KS; Brown MK; Hird AW; Hoveyda AH
J Am Chem Soc; 2006 Jun; 128(22):7182-4. PubMed ID: 16734469
[TBL] [Abstract][Full Text] [Related]
18. Enantioselective total synthesis of erogorgiaene: applications of asymmetric Cu-catalyzed conjugate additions of alkylzincs to acyclic enones.
Cesati RR; de Armas J; Hoveyda AH
J Am Chem Soc; 2004 Jan; 126(1):96-101. PubMed ID: 14709074
[TBL] [Abstract][Full Text] [Related]
19. Lithium binaphtholate-catalyzed enantioselective enyne addition to ketones: access to enynylated tertiary alcohols.
Cai H; Nie J; Zheng Y; Ma JA
J Org Chem; 2014 Jun; 79(12):5484-93. PubMed ID: 24849808
[TBL] [Abstract][Full Text] [Related]
20. Asymmetric Direct 1,2-Addition of Aryl Grignard Reagents to Aryl Alkyl Ketones.
Osakama K; Nakajima M
Org Lett; 2016 Jan; 18(2):236-9. PubMed ID: 26704528
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
