Year |
Citation |
Score |
2007 |
Sparks SM, Chen CL, Martin SF. Tandem Intramolecular Benzyne-Furan Cycloadditions. Total Synthesis of Vineomycinone B(2) Methyl Ester. Tetrahedron. 63: 8619-8635. PMID 18728697 DOI: 10.1016/J.Tet.2007.04.031 |
0.753 |
|
2007 |
Martin S, Chen C, Sparks S. Synthesis of Vineomycinone B2 Methyl Ester Synfacts. 2007: 0236-0236. DOI: 10.1055/S-2007-968187 |
0.615 |
|
2006 |
Chen CL, Sparks SM, Martin SF. C-Aryl glycosides via tandem intramolecular benzyne-furan cycloadditions. Total synthesis of vineomycinone B2 methyl ester. Journal of the American Chemical Society. 128: 13696-7. PMID 17044691 DOI: 10.1021/Ja0652619 |
0.71 |
|
2004 |
Sparks SM, Chow CP, Zhu L, Shea KJ. Type 2 intramolecular N-acylnitroso Diels-Alder reaction: scope and application to the synthesis of medium ring lactams. The Journal of Organic Chemistry. 69: 3025-35. PMID 15104440 DOI: 10.1021/Jo049897Z |
0.812 |
|
2003 |
Kaelin DE, Sparks SM, Plake HR, Martin SF. Regioselective synthesis of unsymmetrical C-aryl glycosides using silicon tethers as disposable linkers. Journal of the American Chemical Society. 125: 12994-5. PMID 14570450 DOI: 10.1021/Ja0375582 |
0.707 |
|
2003 |
Sparks SM, Gutierrez AJ, Shea KJ. Preparation of perhydroisoquinolines via the intramolecular Diels-Alder reaction of N-3,5-hexadienoyl ethyl acrylimidates: a formal synthesis of (+/-)-reserpine. The Journal of Organic Chemistry. 68: 5274-85. PMID 12816489 DOI: 10.1021/Jo0341362 |
0.62 |
|
2002 |
Chow CP, Shea KJ, Sparks SM. Type 2 intramolecular N-acylnitroso diels-alder reaction: stereoselective synthesis of bridged bicyclic oxazinolactams. Organic Letters. 4: 2637-40. PMID 12153197 DOI: 10.1021/Ol026075K |
0.811 |
|
2002 |
Chow CP, Shea KJ, Sparks SM. Type 2 intramolecular N-Acylnitroso Diels - Alder reaction: Stereoselective synthesis of bridged bicyclic oxazinolactams Organic Letters. 4: 2637-2640. DOI: 10.1021/ol026075k |
0.807 |
|
2001 |
Sparks SM, Shea KJ. Vinyl imidates in cycloaddition reactions: a formal synthesis of (+/-)-reserpine. Organic Letters. 3: 2265-7. PMID 11463292 DOI: 10.1021/Ol015988W |
0.755 |
|
2001 |
Bear BR, Sparks SM, Shea KJ. The Type 2 Intramolecular Diels-Alder Reaction: Synthesis and Chemistry of Bridgehead Alkenes. Angewandte Chemie (International Ed. in English). 40: 820-849. PMID 11241630 DOI: 10.1002/1521-3773(20010302)40:5<820::Aid-Anie820>3.0.Co;2-F |
0.793 |
|
2001 |
Sparks SM, Shea KJ. Vinyl imidates in cycloaddition reactions: A formal synthesis of (±)-reserpine Organic Letters. 3: 2265-2267. DOI: 10.1021/ol015988w |
0.621 |
|
2001 |
Bear BR, Sparks SM, Shea KJ. Intramolekulare Diels-Alder-Reaktion vom Typ 2: Synthese und Chemie von Brückenkopf-Alkenen Angewandte Chemie. 113: 864-894. DOI: 10.1002/1521-3757(20010302)113:5<864::Aid-Ange864>3.0.Co;2-0 |
0.703 |
|
2000 |
Sparks SM, Vargas JD, Shea KJ. Type 2 intramolecular nitroso Diels-Alder reaction. Synthesis and structure of bridgehead oxazinolactams. Organic Letters. 2: 1473-5. PMID 10814476 DOI: 10.1021/Ol005811M |
0.746 |
|
2000 |
Sparks SM, Shea KJ. Vinyl imidates in cycloaddition reactions: Synthesis of (±)-alloyohimbane Tetrahedron Letters. 41: 6721-6724. DOI: 10.1016/S0040-4039(00)01093-5 |
0.673 |
|
2000 |
Sparks SM, Shea KJ. ChemInform Abstract: Vinyl Imidates in Cycloaddition Reactions: Synthesis of (.+-.)-Alloyohimbane. Cheminform. 31: no-no. DOI: 10.1002/chin.200050208 |
0.734 |
|
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