Year |
Citation |
Score |
2010 |
Paquette LA, Owen DR, Bibart RT, Seekamp CK, Kahane AL, Lanter JC, Alvarez Corral M. ChemInform Abstract: 1-Oxaspiro[4.4]nonan-6-ones. Synthetic Access via Oxonium Ion Technology, Optical Resolution, and Conversion into Enantiopure Spirocyclic α,β-Butenolides. Cheminform. 32: no-no. DOI: 10.1002/chin.200136107 |
0.664 |
|
2008 |
Luke GP, Seekamp CK, Wang ZQ, Chenard BL. An efficient preparation of beta-aryl-beta-ketophosphonates by the TFAA/H3PO4-mediated acylation of arenes with phosphonoacetic acids. The Journal of Organic Chemistry. 73: 6397-400. PMID 18642870 DOI: 10.1021/Jo800973E |
0.393 |
|
2005 |
Paquette LA, Tian Z, Seekamp CK, Wang T. Synthesis of the cyclopentyl nucleoside (-)-neplanocin A from D-glucose via zirconocene-mediated ring contraction Helvetica Chimica Acta. 88: 1185-1198. DOI: 10.1002/Hlca.200590099 |
0.461 |
|
2004 |
Paquette LA, Seekamp CK, Kahane AL, Hilmey DG, Gallucci J. Stereochemical features of Lewis acid-promoted glycosidations involving 4'-spiroannulated DNA building blocks. The Journal of Organic Chemistry. 69: 7442-7. PMID 15497968 DOI: 10.1021/Jo048904G |
0.701 |
|
2004 |
Paquette LA, Kahane AL, Seekamp CK. Conformationally constrained purine mimics. Incorporation of adenine and guanine into spirocyclic nucleosides. The Journal of Organic Chemistry. 69: 5555-62. PMID 15307723 DOI: 10.1021/Jo049413Z |
0.673 |
|
2003 |
Paquette LA, Seekamp CK, Kahane AL. Conformational restriction of nucleosides by spirocyclic annulation at C4' including synthesis of the complementary dideoxy and didehydrodideoxy analogues. The Journal of Organic Chemistry. 68: 8614-24. PMID 14575494 DOI: 10.1021/Jo0301954 |
0.693 |
|
2001 |
Paquette LA, Owen DR, Bibart RT, Seekamp CK. Spirocyclic restriction of nucleosides. An analysis of protecting group feasibility while accessing prototype anti-1-oxaspiro[4.4]nonanyl mimics. Organic Letters. 3: 4043-5. PMID 11735580 DOI: 10.1021/Ol010212G |
0.538 |
|
2001 |
Paquette LA, Bibart RT, Seekamp CK, Kahane AL. Spirocyclic restriction of nucleosides. Synthesis of the first exemplary syn-1-oxaspiro[4.4]nonanyl member. Organic Letters. 3: 4039-41. PMID 11735579 DOI: 10.1021/Ol010209X |
0.697 |
|
2001 |
Paquette LA, Owen DR, Bibart RT, Seekamp CK, Kahane AL, Lanter JC, Corral MA. 1-Oxaspiro[4.4]nonan-6-ones. Synthetic access via oxonium ion technology, optical resolution, and conversion into enantiopure spirocyclic alpha,beta-butenolides. The Journal of Organic Chemistry. 66: 2828-34. PMID 11304208 DOI: 10.1021/Jo010026O |
0.707 |
|
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