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.
178 related articles for article (PubMed ID: 34436899)
1. Confinement-Controlled, Either Amatov T; Tsuji N; Maji R; Schreyer L; Zhou H; Leutzsch M; List B J Am Chem Soc; 2021 Sep; 143(36):14475-14481. PubMed ID: 34436899 [TBL] [Abstract][Full Text] [Related]
2. Confined acids catalyze asymmetric single aldolizations of acetaldehyde enolates. Schreyer L; Kaib PSJ; Wakchaure VN; Obradors C; Properzi R; Lee S; List B Science; 2018 Oct; 362(6411):216-219. PubMed ID: 30309951 [TBL] [Abstract][Full Text] [Related]
3. Approaching sub-ppm-level asymmetric organocatalysis of a highly challenging and scalable carbon-carbon bond forming reaction. Bae HY; Höfler D; Kaib PSJ; Kasaplar P; De CK; Döhring A; Lee S; Kaupmees K; Leito I; List B Nat Chem; 2018 Aug; 10(8):888-894. PubMed ID: 29988150 [TBL] [Abstract][Full Text] [Related]
4. Triflimide: An Overlooked High-Performance Catalyst of the Mukaiyama Aldol Reaction of Silyl Ketene Acetals with Ketones. Bae HY; List B Chemistry; 2018 Sep; 24(52):13767-13772. PubMed ID: 29943495 [TBL] [Abstract][Full Text] [Related]
5. Chiral primary-tertiary diamine-Brønsted acid salt catalyzed syn-selective cross-aldol reaction of aldehydes. Li J; Fu N; Li X; Luo S; Cheng JP J Org Chem; 2010 Jul; 75(13):4501-7. PubMed ID: 20521772 [TBL] [Abstract][Full Text] [Related]
6. Stereodefined Acyclic Polysubstituted Silyl Ketene Aminals: Asymmetric Formation of Aldol Products with Quaternary Carbon Stereocenters. Nairoukh Z; Marek I Angew Chem Int Ed Engl; 2015 Nov; 54(48):14393-7. PubMed ID: 26448575 [TBL] [Abstract][Full Text] [Related]
7. BINAP/AgOTf/KF/18-crown-6 as new bifunctional catalysts for asymmetric Sakurai-Hosomi allylation and Mukaiyama aldol reaction. Wadamoto M; Ozasa N; Yanagisawa A; Yamamoto H J Org Chem; 2003 Jul; 68(14):5593-601. PubMed ID: 12839451 [TBL] [Abstract][Full Text] [Related]
8. Acetaldehyde Silyl Enol Ethers in Enantioselective Mukaiyama Aldol Reactions: Enzyme-Like Organocatalysis in Action. Dell'Amico L; Zanardi F Angew Chem Int Ed Engl; 2019 Mar; 58(11):3264-3266. PubMed ID: 30730598 [TBL] [Abstract][Full Text] [Related]
9. The stereoselective synthesis of α-amino aldols starting from terminal alkynes. Miura T; Nakamuro T; Hiraga K; Murakami M Chem Commun (Camb); 2014 Sep; 50(72):10474-7. PubMed ID: 25068433 [TBL] [Abstract][Full Text] [Related]
11. Highly enantioselective synthesis of syn-aldols of cyclohexanones via chiral primary amine catalyzed asymmetric transfer aldol reactions in ionic liquid. Zhou P; Luo S; Cheng JP Org Biomol Chem; 2011 Mar; 9(6):1784-90. PubMed ID: 21264400 [TBL] [Abstract][Full Text] [Related]
12. The exceptional chelating ability of dimethylaluminum chloride and methylaluminum dichloride. The merged stereochemical impact of alpha- and beta-stereocenters in chelate-controlled carbonyl addition reactions with enolsilane and hydride nucleophiles. Evans DA; Allison BD; Yang MG; Masse CE J Am Chem Soc; 2001 Nov; 123(44):10840-52. PubMed ID: 11686685 [TBL] [Abstract][Full Text] [Related]
13. Second Generation of Aldol Reaction. Gati W; Yamamoto H Acc Chem Res; 2016 Sep; 49(9):1757-68. PubMed ID: 27513812 [TBL] [Abstract][Full Text] [Related]
14. Catalytic asymmetric assembly of stereodefined propionate units: an enantioselective total synthesis of (-)-pironetin. Shen X; Wasmuth AS; Zhao J; Zhu C; Nelson SG J Am Chem Soc; 2006 Jun; 128(23):7438-9. PubMed ID: 16756287 [TBL] [Abstract][Full Text] [Related]
15. FeCl3·6H2O-catalyzed Mukaiyama-aldol type reactions of enolizable aldehydes and acetals. Rodríguez-Gimeno A; Cuenca AB; Gil-Tomás J; Medio-Simón M; Olmos A; Asensio G J Org Chem; 2014 Sep; 79(17):8263-70. PubMed ID: 25102027 [TBL] [Abstract][Full Text] [Related]
16. A designer axially chiral amino sulfonamide as an efficient organocatalyst for direct asymmetric anti-selective Mannich reactions and syn-selective cross-aldol reactions. Kano T; Yamaguchi Y; Maruoka K Chemistry; 2009 Jul; 15(27):6678-87. PubMed ID: 19479934 [TBL] [Abstract][Full Text] [Related]
17. Diastereo- and Enantioselective Construction of Stereochemical Arrays Exploiting Non-Classical Hydrogen Bonding in Enolborates. Li M; Scheeff S; Chen J; Johnston RC; Rizzo A; Krenske EH; Chiu P Chemistry; 2024 Aug; 30(46):e202401485. PubMed ID: 38829820 [TBL] [Abstract][Full Text] [Related]
18. ESTER DERIVED TITANIUM ENOLATE ALDOL REACTION: HIGHLY DIASTEREOSELECTIVE SYNTHESIS OF SYN- AND ANTI-ALDOLS. Ghosh AK; Fidanze S; Onishi M; Hussain KA Tetrahedron Lett; 1997 Oct; 38(41):7171-7174. PubMed ID: 30407471 [TBL] [Abstract][Full Text] [Related]
19. Mukaiyama aldol addition to alpha-chloro-substituted aldehydes. Origin of the unexpected syn selectivity. Borg T; Danielsson J; Somfai P Chem Commun (Camb); 2010 Feb; 46(8):1281-3. PubMed ID: 20449277 [TBL] [Abstract][Full Text] [Related]
20. [Development of asymmetric synthesis of optically active compounds including fluoroorganic molecules]. Iseki K Yakugaku Zasshi; 1999 Nov; 119(11):787-804. PubMed ID: 10590709 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]