Year |
Citation |
Score |
2015 |
Zhao G, He M, Li H, Duan S, Yuan Z, Xie X, She X. Domino intramolecular Diels-Alder reactions to construct a 6/6/5/5 fused tetracyclic framework. Chemical Communications (Cambridge, England). PMID 26463746 DOI: 10.1039/C5Cc06923H |
0.302 |
|
2015 |
Chen X, Duan S, Tao C, Zhai H, Qiu FG. Total synthesis of (+)-gelsemine via an organocatalytic Diels-Alder approach. Nature Communications. 6: 7204. PMID 25995149 DOI: 10.1038/Ncomms8204 |
0.311 |
|
2011 |
Patti RK, Duan S, Wang Z, Herndon JW. Preparation of phenalenes and hydronaphthacenes through tandem alkyne Fischer-carbene complex coupling and inter- or intramolecular Diels-Alder reactions. Tetrahedron Letters. 52: 4182-4185. PMID 21857755 DOI: 10.1016/J.Tetlet.2011.06.006 |
0.655 |
|
2010 |
Kumar-Patti R, Duan S, Camacho-Davila A, Waynant K, Dunn KA, Herndon JW. Synthesis of hydronaphthalenes through coupling of enyne carbonyl compounds that contain pendant alkene groups with Fischer carbene complexes. Tetrahedron Letters. 51: 3682-3684. PMID 20548964 DOI: 10.1016/J.Tetlet.2010.05.049 |
0.672 |
|
2009 |
Duan S, Jana R, Tunge JA. Lewis acid-catalyzed diastereoselective hydroarylation of benzylidene malonic esters. The Journal of Organic Chemistry. 74: 4612-4. PMID 19518152 DOI: 10.1021/Jo900367G |
0.328 |
|
2008 |
Duan S, Sinha-Mahapatra DK, Herndon JW. Synthesis of naphthalenes through three-component coupling of alkynes, Fischer carbene complexes, and benzaldehyde hydrazones via isoindole intermediates. Organic Letters. 10: 1541-4. PMID 18351767 DOI: 10.1021/Ol800242N |
0.679 |
|
2007 |
Duan S, Cress K, Waynant K, Ramos-Miranda E, Herndon JW. Synthesis of alkylidenephthalans through fluoride-induced cyclization of electron-deficient 2-siloxymethylphenylacetylene derivatives. Tetrahedron. 63: 2959-2965. PMID 18382602 DOI: 10.1016/J.Tet.2007.01.046 |
0.752 |
|
2006 |
Ghorai BK, Duan S, Jiang D, Herndon JW. Coupling of β-cyanocarbene-chromium complexes with 2-alkynylbenzoyl derivatives: A [5+5]-cycloaddition approach to phenanthridines Synthesis. 3661-3669. DOI: 10.1055/S-2006-950286 |
0.656 |
|
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