Search Results - "Parrish, Jonathan D."

[3+2] Photooxygenation of aryl cyclopropanes via visible light photocatalysis by Lu, Zhan, Parrish, Jonathan D., Yoon, Tehshik P.

“…We report that Ru(bpz)32+ is an excellent sensitizer for the photooxygenation of aryl cyclopropanes upon irradiation with visible light. The effectiveness of…”
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Endoperoxide Synthesis by Photocatalytic Aerobic [2 + 2 + 2] Cycloadditions by Parrish, Jonathan D, Ischay, Michael A, Lu, Zhan, Guo, Song, Peters, Noël R, Yoon, Tehshik P

“…Structurally novel endoperoxides can be sythesized by the photocatalytic cyclotrimerization of bis(styrene) substrates with molecular oxygen. The optimal…”
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Enantioselective Total Synthesis of Brevetoxin A: Unified Strategy for the B, E, G, and J Subunits by Crimmins, Michael T., Ellis, J. Michael, Emmitte, Kyle A., Haile, Pamela A., McDougall, Patrick J., Parrish, Jonathan D., Zuccarello, J. Lucas

“…Brevetoxin A is a decacyclic ladder toxin that possesses 5‐, 6‐, 7‐, 8‐, and 9‐membered oxacycles, as well as 22 tetrahedral stereocenters. Herein, we describe…”
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Total Synthesis of Brevetoxin A by Crimmins, Michael T, Zuccarello, J. Lucas, Ellis, J. Michael, McDougall, Patrick J, Haile, Pamela A, Parrish, Jonathan D, Emmitte, Kyle A

“…A total synthesis of brevetoxin A is reported. Two tetracyclic coupling partners, prepared from previously reported advanced fragments, were effectively united…”
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Convergent, Stereoselective Synthesis of the GHIJ Fragment of Brevetoxin A by Crimmins, Michael T, Zuccarello, J. Lucas, Cleary, Pamela A, Parrish, Jonathan D

“…A stereoselective synthesis of the GHIJ fragment of brevetoxin A utilizing a convergent assembly strategy is described. Glycolate alkylation, ring-closing…”
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[3+2] Photooxygenation of aryl cylopropanes via visible light photocatalysis by Lu, Zhan, Parrish, Jonathan D, Yoon, Tehshik P

“…We report that Ru(bpz) is an excellent sensitizer for the photooxygenation of aryl cyclopropanes upon irradiation with visible light. The effectiveness of this…”
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Novel 2,3,4,5-tetrahydro-benzo[d]azepine derivatives of 2,4-diaminopyrimidine, selective and orally bioavailable ALK inhibitors with antitumor efficacy in ALCL mouse models by Mesaros, Eugen F., Burke, Jason P., Parrish, Jonathan D., Dugan, Benjamin J., Anzalone, Andrew V., Angeles, Thelma S., Albom, Mark S., Aimone, Lisa D., Quail, Matthew R., Wan, Weihua, Lu, Lihui, Huang, Zeqi, Ator, Mark A., Ruggeri, Bruce A., Cheng, Mangeng, Ott, Gregory R., Dorsey, Bruce D.

“…The synthesis and biological evaluation of potent and selective anaplastic lymphoma kinase (ALK) inhibitors from a novel class of 2,4-diaminopyrimidines,…”
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Corrigendum to “Novel 2,3,4,5-tetrahydro-benzo[ d]azepine derivatives of 2,4-diaminopyrimidine, selective and orally bioavailable ALK inhibitors with antitumor efficacy in ALCL mouse models” [Bioorg. Med. Chem. Lett. 21 (2011) 463] by Mesaros, Eugen F., Burke, Jason P., Parrish, Jonathan D., Dugan, Benjamin J., Anzalone, Andrew V., Angeles, Thelma S., Albom, Mark S., Aimone, Lisa D., Quail, Matthew R., Wan, Weihua, Lu, Lihui, Huang, Zeqi, Ator, Mark A., Ruggeri, Bruce A., Cheng, Mangeng, Ott, Gregory R., Dorsey, Bruce D.

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