190 related articles for article (PubMed ID: 18533665)
1. Ruthenium catalyzed C-C bond formation via transfer hydrogenation: branch-selective reductive coupling of allenes to paraformaldehyde and higher aldehydes.
Ngai MY; Skucas E; Krische MJ
Org Lett; 2008 Jul; 10(13):2705-8. PubMed ID: 18533665
[TBL] [Abstract][Full Text] [Related]
2. Diene hydroacylation from the alcohol or aldehyde oxidation level via ruthenium-catalyzed C-C bond-forming transfer hydrogenation: synthesis of beta,gamma-unsaturated ketones.
Shibahara F; Bower JF; Krische MJ
J Am Chem Soc; 2008 Oct; 130(43):14120-2. PubMed ID: 18841895
[TBL] [Abstract][Full Text] [Related]
3. Ruthenium-catalyzed C-C coupling of fluorinated alcohols with allenes: dehydrogenation at the energetic limit of β-hydride elimination.
Sam B; Luong T; Krische MJ
Angew Chem Int Ed Engl; 2015 Apr; 54(18):5465-9. PubMed ID: 25757459
[TBL] [Abstract][Full Text] [Related]
4. anti-Aminoallylation of aldehydes via ruthenium-catalyzed transfer hydrogenative coupling of sulfonamido allenes: 1,2-aminoalcohols.
Skucas E; Zbieg JR; Krische MJ
J Am Chem Soc; 2009 Apr; 131(14):5054-5. PubMed ID: 19317402
[TBL] [Abstract][Full Text] [Related]
5. Amplification of anti-diastereoselectivity via Curtin-Hammett effects in ruthenium-catalyzed hydrohydroxyalkylation of 1,1-disubstituted allenes: diastereoselective formation of all-carbon quaternary centers.
Zbieg JR; McInturff EL; Leung JC; Krische MJ
J Am Chem Soc; 2011 Feb; 133(4):1141-4. PubMed ID: 21175178
[TBL] [Abstract][Full Text] [Related]
6. Ruthenium-catalyzed C-C bond forming transfer hydrogenation: carbonyl allylation from the alcohol or aldehyde oxidation level employing acyclic 1,3-dienes as surrogates to preformed allyl metal reagents.
Shibahara F; Bower JF; Krische MJ
J Am Chem Soc; 2008 May; 130(20):6338-9. PubMed ID: 18444617
[TBL] [Abstract][Full Text] [Related]
7. Direct ruthenium-catalyzed C-C coupling of ethanol: diene hydro-hydroxyethylation to form all-carbon quaternary centers.
Han H; Krische MJ
Org Lett; 2010 Jun; 12(12):2844-6. PubMed ID: 20491487
[TBL] [Abstract][Full Text] [Related]
8. Direct vinylation of alcohols or aldehydes employing alkynes as vinyl donors: a ruthenium catalyzed C-C bond-forming transfer hydrogenation.
Patman RL; Chaulagain MR; Williams VM; Krische MJ
J Am Chem Soc; 2009 Feb; 131(6):2066-7. PubMed ID: 19173651
[TBL] [Abstract][Full Text] [Related]
9. Regioselective Hydrohydroxyalkylation of Styrene with Primary Alcohols or Aldehydes via Ruthenium-Catalyzed C-C Bond Forming Transfer Hydrogenation.
Xiao H; Wang G; Krische MJ
Angew Chem Int Ed Engl; 2016 Dec; 55(52):16119-16122. PubMed ID: 27910228
[TBL] [Abstract][Full Text] [Related]
10. Alkyne-aldehyde reductive C-C coupling through ruthenium-catalyzed transfer hydrogenation: direct regio- and stereoselective carbonyl vinylation to form trisubstituted allylic alcohols in the absence of premetallated reagents.
Leung JC; Patman RL; Sam B; Krische MJ
Chemistry; 2011 Oct; 17(44):12437-43. PubMed ID: 21953608
[TBL] [Abstract][Full Text] [Related]
11. All-carbon quaternary centers via ruthenium-catalyzed hydroxymethylation of 2-substituted butadienes mediated by formaldehyde: beyond hydroformylation.
Smejkal T; Han H; Breit B; Krische MJ
J Am Chem Soc; 2009 Aug; 131(30):10366-7. PubMed ID: 19594163
[TBL] [Abstract][Full Text] [Related]
12. Enantioselective ruthenium-catalyzed carbonyl allylation via alkyne-alcohol C-C bond-forming transfer hydrogenation: allene hydrometalation vs oxidative coupling.
Liang T; Nguyen KD; Zhang W; Krische MJ
J Am Chem Soc; 2015 Mar; 137(9):3161-4. PubMed ID: 25734220
[TBL] [Abstract][Full Text] [Related]
13. Ruthenium catalyzed reductive coupling of paraformaldehyde to trifluoromethyl allenes: CF3-bearing all-carbon quaternary centers.
Sam B; Montgomery TP; Krische MJ
Org Lett; 2013 Jul; 15(14):3790-3. PubMed ID: 23841678
[TBL] [Abstract][Full Text] [Related]
14. Ruthenium-catalyzed reductive coupling of 1,3-enynes and aldehydes by transfer hydrogenation: anti-diastereoselective carbonyl propargylation.
Geary LM; Leung JC; Krische MJ
Chemistry; 2012 Dec; 18(52):16823-7. PubMed ID: 23147989
[TBL] [Abstract][Full Text] [Related]
15. Ruthenium-Catalyzed Transfer Hydrogenation for C-C Bond Formation: Hydrohydroxyalkylation and Hydroaminoalkylation via Reactant Redox Pairs.
Perez F; Oda S; Geary LM; Krische MJ
Top Curr Chem (Cham); 2016 Jun; 374(3):35. PubMed ID: 27573275
[TBL] [Abstract][Full Text] [Related]
16. Cyclometalated Iridium-PhanePhos Complexes Are Active Catalysts in Enantioselective Allene-Fluoral Reductive Coupling and Related Alcohol-Mediated Carbonyl Additions That Form Acyclic Quaternary Carbon Stereocenters.
Schwartz LA; Holmes M; Brito GA; Gonçalves TP; Richardson J; Ruble JC; Huang KW; Krische MJ
J Am Chem Soc; 2019 Feb; 141(5):2087-2096. PubMed ID: 30681850
[TBL] [Abstract][Full Text] [Related]
17. Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level via transfer hydrogenative coupling of allyl acetate: departure from chirally modified allyl metal reagents in carbonyl addition.
Kim IS; Ngai MY; Krische MJ
J Am Chem Soc; 2008 Nov; 130(44):14891-9. PubMed ID: 18841896
[TBL] [Abstract][Full Text] [Related]
18. Successive C-C coupling of dienes to vicinally dioxygenated hydrocarbons: ruthenium catalyzed [4 + 2] cycloaddition across the diol, hydroxycarbonyl, or dione oxidation levels.
Geary LM; Glasspoole BW; Kim MM; Krische MJ
J Am Chem Soc; 2013 Mar; 135(10):3796-9. PubMed ID: 23448269
[TBL] [Abstract][Full Text] [Related]
19. Catalytic C-C coupling via transfer hydrogenation: reverse prenylation, crotylation, and allylation from the alcohol or aldehyde oxidation level.
Bower JF; Skucas E; Patman RL; Krische MJ
J Am Chem Soc; 2007 Dec; 129(49):15134-5. PubMed ID: 18020342
[No Abstract] [Full Text] [Related]
20. Enantioselective carbonyl reverse prenylation from the alcohol or aldehyde oxidation level employing 1,1-dimethylallene as the prenyl donor.
Han SB; Kim IS; Han H; Krische MJ
J Am Chem Soc; 2009 May; 131(20):6916-7. PubMed ID: 19453190
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]