Audrey Graham Ross - Publications
Affiliations: | 2012 | Chemistry | Columbia University, New York, NY |
Year | Citation | Score | |||
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2014 | Townsend SD, Ross AG, Liu K, Danishefsky SJ. Stereospecific cis- and trans-ring fusions arising from common intermediates. Proceedings of the National Academy of Sciences of the United States of America. 111: 7931-5. PMID 24843125 DOI: 10.1073/Pnas.1407613111 | 0.524 | |||
2014 | Pham HV, Paton RS, Ross AG, Danishefsky SJ, Houk KN. Intramolecular Diels-Alder reactions of cycloalkenones: stereoselectivity, Lewis acid acceleration, and halogen substituent effects. Journal of the American Chemical Society. 136: 2397-403. PMID 24410341 DOI: 10.1021/Ja410220W | 0.495 | |||
2013 | Ross AG, Townsend SD, Danishefsky SJ. Halocycloalkenones as Diels-Alder dienophiles. Applications to generating useful structural patterns. The Journal of Organic Chemistry. 78: 204-10. PMID 23151095 DOI: 10.1021/Jo302230M | 0.533 | |||
2012 | Ross AG, Li X, Danishefsky SJ. Intramolecular Diels-Alder reactions of cycloalkenones: translation of high endo selectivity to trans junctions. Journal of the American Chemical Society. 134: 16080-4. PMID 22950514 DOI: 10.1021/Ja307708Q | 0.507 | |||
2012 | Ross AG, Li X, Danishefsky SJ. Preparation of cyclobutenone Organic Syntheses. 89: 491-500. DOI: 10.1002/0471264229.Os089.47 | 0.425 | |||
2011 | Paton RS, Kim S, Ross AG, Danishefsky SJ, Houk KN. Experimental Diels-Alder reactivities of cycloalkenones and cyclic dienes explained through transition-state distortion energies. Angewandte Chemie (International Ed. in English). 50: 10366-8. PMID 21910195 DOI: 10.1002/Anie.201103998 | 0.413 | |||
2010 | Snyder SA, Sherwood TC, Ross AG. Total syntheses of dalesconol A and B. Angewandte Chemie (International Ed. in English). 49: 5146-50. PMID 20572237 DOI: 10.1002/Anie.201002264 | 0.312 | |||
2009 | Snyder SA, Breazzano SP, Ross AG, Lin Y, Zografos AL. Total synthesis of diverse carbogenic complexity within the resveratrol class from a common building block. Journal of the American Chemical Society. 131: 1753-65. PMID 19143488 DOI: 10.1021/Ja806183R | 0.319 | |||
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