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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
258 related items for PubMed ID: 19453190
1. 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 27; 131(20):6916-7. PubMed ID: 19453190 [Abstract] [Full Text] [Related]
2. anti-Diastereo- and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level employing a cyclometallated iridium catalyst: alpha-methyl allyl acetate as a surrogate to preformed crotylmetal reagents. Kim IS, Han SB, Krische MJ. J Am Chem Soc; 2009 Feb 25; 131(7):2514-20. PubMed ID: 19191498 [Abstract] [Full Text] [Related]
3. Diastereo- and enantioselective anti-alkoxyallylation employing allylic gem-dicarboxylates as allyl donors via iridium-catalyzed transfer hydrogenation. Han SB, Han H, Krische MJ. J Am Chem Soc; 2010 Feb 17; 132(6):1760-1. PubMed ID: 20099821 [Abstract] [Full Text] [Related]
4. anti-Diastereo- and enantioselective carbonyl (hydroxymethyl)allylation from the alcohol or aldehyde oxidation level: allyl carbonates as allylmetal surrogates. Zhang YJ, Yang JH, Kim SH, Krische MJ. J Am Chem Soc; 2010 Apr 07; 132(13):4562-3. PubMed ID: 20225853 [Abstract] [Full Text] [Related]
5. 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 05; 130(44):14891-9. PubMed ID: 18841896 [Abstract] [Full Text] [Related]
7. Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level using allyl acetate as an allyl metal surrogate. Kim IS, Ngai MY, Krische MJ. J Am Chem Soc; 2008 May 21; 130(20):6340-1. PubMed ID: 18444616 [Abstract] [Full Text] [Related]
9. 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 06; 141(5):2087-2096. PubMed ID: 30681850 [Abstract] [Full Text] [Related]
10. 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 29; 130(43):14120-2. PubMed ID: 18841895 [Abstract] [Full Text] [Related]
18. 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 11; 137(9):3161-4. PubMed ID: 25734220 [Abstract] [Full Text] [Related]
19. 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 02; 133(4):1141-4. PubMed ID: 21175178 [Abstract] [Full Text] [Related]
20. Diastereo- and Enantioselective Iridium Catalyzed Coupling of Vinyl Aziridines with Alcohols: Site-Selective Modification of Unprotected Diols and Synthesis of Substituted Piperidines. Wang G, Franke J, Ngo CQ, Krische MJ. J Am Chem Soc; 2015 Jun 24; 137(24):7915-20. PubMed ID: 26074091 [Abstract] [Full Text] [Related] Page: [Next] [New Search]