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.
104 related articles for article (PubMed ID: 31274327)
1. Total Synthesis of Hoiamide A Using an Evans-Tishchenko Reaction as a Key Step. Guo Y; Zhou J; Gao B; Zhao M; Yan JL; Xu Z; Choi S; Ye T Org Lett; 2019 Jul; 21(14):5471-5474. PubMed ID: 31274327 [TBL] [Abstract][Full Text] [Related]
2. Directed hydrogenations and an Ireland-Claisen rearrangement linked to evans-tishchenko chemistry: the highly efficient total synthesis of the marine cyclodepsipeptide doliculide. Chen T; Altmann KH Chemistry; 2015 Jun; 21(23):8403-7. PubMed ID: 25917788 [TBL] [Abstract][Full Text] [Related]
4. Stereoselective Installation of Five Contiguous Stereogenic Centers in a Double Aldol-Tishchenko Cascade and Evaluation of the Key Transition State through DFT Calculation. Mackey P; Turlik A; Ando K; Light ME; Houk KN; McGlacken GP Org Lett; 2021 Aug; 23(16):6372-6376. PubMed ID: 34374288 [TBL] [Abstract][Full Text] [Related]
5. Direct enantioselective aldol-Tishchenko reaction catalyzed by chiral lithium diphenylbinaphtholate. Ichibakase T; Nakajima M Org Lett; 2011 Apr; 13(7):1579-81. PubMed ID: 21355567 [TBL] [Abstract][Full Text] [Related]
7. Asymmetric Aldol-Tishchenko Reaction of Sulfinimines. Foley VM; McSweeney CM; Eccles KS; Lawrence SE; McGlacken GP Org Lett; 2015 Nov; 17(22):5642-5. PubMed ID: 26528888 [TBL] [Abstract][Full Text] [Related]
8. Samarium Ion-Promoted Cross-Aldol Reactions and Tandem Aldol/Evans-Tishchenko Reactions. Lu L; Chang HY; Fang JM J Org Chem; 1999 Feb; 64(3):843-853. PubMed ID: 11674156 [TBL] [Abstract][Full Text] [Related]
9. Total synthesis of sphingofungin F based on chiral tricyclic iminolactone. Gan FF; Yang SB; Luo YC; Yang WB; Xu PF J Org Chem; 2010 Apr; 75(8):2737-40. PubMed ID: 20329736 [TBL] [Abstract][Full Text] [Related]
10. Asymmetric synthesis of a stereopentade fragment toward latrunculins. Joyeux B; Gamet A; Casaretto N; Nay B Beilstein J Org Chem; 2023; 19():428-433. PubMed ID: 37091733 [TBL] [Abstract][Full Text] [Related]
11. An Evans-Tishchenko-ring-closing metathesis approach to medium-ring lactones. Aird JI; Hulme AN; White JW Org Lett; 2007 Feb; 9(4):631-4. PubMed ID: 17256949 [TBL] [Abstract][Full Text] [Related]
12. Stereoselective Synthesis of 2-Fluoro-1,3-Diols via Lithium Binaphtholate-Catalyzed Aldol-Tishchenko Reaction. Asano T; Kotani S; Nakajima M Org Lett; 2019 Jun; 21(11):4192-4196. PubMed ID: 31120256 [TBL] [Abstract][Full Text] [Related]
13. Total synthesis of cruentaren B. Chakraborty TK; Chattopadhyay AK J Org Chem; 2008 May; 73(9):3578-81. PubMed ID: 18363370 [TBL] [Abstract][Full Text] [Related]
14. A formal total synthesis of the salicylihalamides. Herb C; Maier ME J Org Chem; 2003 Oct; 68(21):8129-35. PubMed ID: 14535794 [TBL] [Abstract][Full Text] [Related]
15. Involvement of JNK and caspase activation in hoiamide A-induced neurotoxicity in neocortical neurons. Cao Z; Li X; Zou X; Greenwood M; Gerwick WH; Murray TF Mar Drugs; 2015 Feb; 13(2):903-19. PubMed ID: 25675001 [TBL] [Abstract][Full Text] [Related]
16. Total synthesis of (+)-13-deoxytedanolide. Smith AB; Adams CM; Lodise Barbosa SA; Degnan AP J Am Chem Soc; 2003 Jan; 125(2):350-1. PubMed ID: 12517144 [TBL] [Abstract][Full Text] [Related]
17. Addition-elimination versus Tishchenko reaction in the gas phase. Wilenska B; Swider P; Danikiewicz W J Mass Spectrom; 2014 Dec; 49(12):1247-53. PubMed ID: 25476942 [TBL] [Abstract][Full Text] [Related]
18. Mechanistic origin of cross-coupling selectivity in Ni-catalysed Tishchenko reactions. Yu H; Fu Y Chemistry; 2012 Dec; 18(52):16765-73. PubMed ID: 23112051 [TBL] [Abstract][Full Text] [Related]
19. Homoleptic lanthanide amides as homogeneous catalysts for alkyne hydroamination and the Tishchenko reaction. Bürgstein MR; Berberich H; Roesky PW Chemistry; 2001 Jul; 7(14):3078-85. PubMed ID: 11495435 [TBL] [Abstract][Full Text] [Related]