Year |
Citation |
Score |
2018 |
El Anwar S, Laila Z, Ramsubhag R, Tlais S, Safa A, Dudley G, Naoufal D. Synthesis and characterization of click-decahydrodecaborate derivatives by the copper(I) catalyzed [3+2] azide-alkyne cycloaddition reaction Journal of Organometallic Chemistry. 865: 89-94. DOI: 10.1016/J.Jorganchem.2018.01.039 |
0.597 |
|
2014 |
Tlais SF, Danheiser RL. N-tosyl-3-azacyclohexyne. Synthesis and chemistry of a strained cyclic ynamide. Journal of the American Chemical Society. 136: 15489-92. PMID 25328003 DOI: 10.1021/Ja509055R |
0.55 |
|
2012 |
Tlais SF, Dudley GB. On the proposed structures and stereocontrolled synthesis of the cephalosporolides. Beilstein Journal of Organic Chemistry. 8: 1287-92. PMID 23019461 DOI: 10.3762/Bjoc.8.146 |
0.636 |
|
2011 |
Robinson JM, Tlais SF, Fong J, Danheiser RL. A [4 + 4] annulation strategy for the synthesis of eight-membered carbocycles based on intramolecular cycloadditions of conjugated enynes. Tetrahedron. 67: 9890-9898. PMID 22267878 DOI: 10.1016/J.Tet.2011.09.031 |
0.589 |
|
2011 |
Tlais SF, Dudley GB. A gold-catalyzed alkyne-diol cycloisomerization for the synthesis of oxygenated 5,5-spiroketals. Beilstein Journal of Organic Chemistry. 7: 570-7. PMID 21647322 DOI: 10.3762/Bjoc.7.66 |
0.642 |
|
2011 |
Yang J, Tummatorn J, Slegeris R, Tlais SF, Dudley GB. Synthesis of the tricyclic core of aldingenin B by oxidative cyclo-ketalization of an alkyne-diol. Organic Letters. 13: 2065-7. PMID 21391664 DOI: 10.1021/Ol200421S |
0.626 |
|
2010 |
Tlais SF, Dudley GB. Stereocontrol of 5,5-spiroketals in the synthesis of cephalosporolide H epimers. Organic Letters. 12: 4698-701. PMID 20860404 DOI: 10.1021/Ol102201Z |
0.641 |
|
2009 |
Tlais SF, Clark RJ, Dudley GB. A striking exception to the chelate model for acyclic diastereocontrol: efficient access to a versatile propargyl alcohol for chemical synthesis. Molecules (Basel, Switzerland). 14: 5216-22. PMID 20032887 DOI: 10.3390/Molecules14125216 |
0.635 |
|
2009 |
Tlais SF, Lam H, House SE, Dudley GB. New strategies for protecting group chemistry: synthesis, reactivity, and indirect oxidative cleavage of para-siletanylbenzyl ethers. The Journal of Organic Chemistry. 74: 1876-85. PMID 19183037 DOI: 10.1021/Jo802229P |
0.607 |
|
2008 |
Albiniak PA, Amisial SM, Dudley GB, Hernandez JP, House SE, Matthews ME, Nwoye EO, Reilly MK, Tlais SF. Stable oxypyridinium triflate (OPT) salts for the synthesis of halobenzyl ethers Synthetic Communications. 38: 656-665. DOI: 10.1080/00397910701818362 |
0.639 |
|
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