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.
152 related articles for article (PubMed ID: 37008159)
21. Synthetic Studies on Spirolides A and B: Formation of the Upper Carbon Framework Based on a Lewis Acid Template-Catalyzed Diels-Alder Reaction. Ishihara J; Usui F; Kurose T; Baba T; Kawaguchi Y; Watanabe Y; Hatakeyama S Chemistry; 2019 Jan; 25(6):1543-1552. PubMed ID: 30357942 [TBL] [Abstract][Full Text] [Related]
22. Catalytic Enantioselective Diels-Alder Reactions of Benzoquinones and Vinylindoles with Chiral Magnesium Phosphate Complexes. Bai Y; Yuan J; Hu X; Antilla JC Org Lett; 2019 Jun; 21(12):4549-4553. PubMed ID: 31150254 [TBL] [Abstract][Full Text] [Related]
23. Catalytic asymmetric diels-alder reaction of quinone imine ketals: a site-divergent approach. Hashimoto T; Nakatsu H; Maruoka K Angew Chem Int Ed Engl; 2015 Apr; 54(15):4617-21. PubMed ID: 25689774 [TBL] [Abstract][Full Text] [Related]
24. Catalytic Asymmetric Aza-Diels-Alder Reaction of Ketimines and Unactivated Dienes. Zhao Q; Li Y; Zhang QX; Cheng JP; Li X Angew Chem Int Ed Engl; 2021 Aug; 60(32):17608-17614. PubMed ID: 34036702 [TBL] [Abstract][Full Text] [Related]
25. A highly enantioselective hetero-Diels-Alder reaction of aldehydes with Danishefsky's diene catalyzed by chiral titanium(IV) 5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2-naphthol complexes. Wang B; Feng X; Huang Y; Liu H; Cui X; Jiang Y J Org Chem; 2002 Apr; 67(7):2175-82. PubMed ID: 11925225 [TBL] [Abstract][Full Text] [Related]
26. Enantioselective oxa-Diels-Alder Sequences of Dendralenes. Fan YM; Yu LJ; Gardiner MG; Coote ML; Sherburn MS Angew Chem Int Ed Engl; 2022 Sep; 61(39):e202204872. PubMed ID: 35900232 [TBL] [Abstract][Full Text] [Related]
27. A catalytic asymmetric hetero-Diels-Alder reaction of olefinic azlactones and isatins: facile access to chiral spirooxindole dihydropyranones. Gao TP; Lin JB; Hu XQ; Xu PF Chem Commun (Camb); 2014 Aug; 50(64):8934-6. PubMed ID: 24976540 [TBL] [Abstract][Full Text] [Related]
28. Catalytic enantioselective Diels-Alder reaction by self-assembly of the components on a Lewis acid template. Ward DE; Souweha MS Org Lett; 2005 Aug; 7(16):3533-6. PubMed ID: 16048335 [TBL] [Abstract][Full Text] [Related]
29. Total Synthesis of (-)-Lepadin F based on a Stereoselective Diels-Alder Reaction Controlled by a Ketolactone-type Dienophile. Gu H; Hu Y; Jia Y; Zhou Q; Luo G; Chen X Chemistry; 2021 Feb; 27(12):4141-4149. PubMed ID: 33289139 [TBL] [Abstract][Full Text] [Related]
30. The preparation and utility of bis(sulfinyl)imidoamidine ligands for the copper-catalyzed Diels-Alder reaction. Owens TD; Souers AJ; Ellman JA J Org Chem; 2003 Jan; 68(1):3-10. PubMed ID: 12515453 [TBL] [Abstract][Full Text] [Related]
31. Development of an unusually highly enantioselective hetero-Diels-Alder reaction of benzaldehyde with activated dienes catalyzed by hypercoordinating chiral aluminum complexes. Simonsen KB; Svenstrup N; Roberson M; Jorgensen KA Chemistry; 2000 Jan; 6(1):123-8. PubMed ID: 10747395 [TBL] [Abstract][Full Text] [Related]
32. Asymmetric Synthesis of Hydrocarbazoles Catalyzed by an Octahedral Chiral-at-Rhodium Lewis Acid. Huang Y; Song L; Gong L; Meggers E Chem Asian J; 2015 Dec; 10(12):2738-43. PubMed ID: 26344422 [TBL] [Abstract][Full Text] [Related]
33. Allylsilane Reagent-Controlled Divergent Asymmetric Catalytic Reactions of 2-Naphthoquinone-1-methide. Lin X; Liu Y; Li C Chemistry; 2020 Nov; 26(62):14173-14180. PubMed ID: 32815199 [TBL] [Abstract][Full Text] [Related]
34. Enantioselective biomimetic total syntheses of kuwanons I and J and brosimones A and B. Han J; Li X; Guan Y; Zhao W; Wulff WD; Lei X Angew Chem Int Ed Engl; 2014 Aug; 53(35):9257-61. PubMed ID: 25044511 [TBL] [Abstract][Full Text] [Related]
35. Asymmetric inverse-electron-demand hetero-Diels-Alder reaction for the construction of bicyclic skeletons with multiple stereocenters by using a bifunctional organocatalytic strategy: an efficient approach to chiral macrolides. Jiang X; Wang L; Kai M; Zhu L; Yao X; Wang R Chemistry; 2012 Sep; 18(36):11465-73. PubMed ID: 22829472 [TBL] [Abstract][Full Text] [Related]