Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Shannon M, Decker"'
Autor:
Brian S, Safina, Steven J, McKerrall, Shaoyi, Sun, Chien-An, Chen, Sultan, Chowdhury, Qi, Jia, Jun, Li, Alla Y, Zenova, Jean-Christophe, Andrez, Girish, Bankar, Philippe, Bergeron, Jae H, Chang, Elaine, Chang, Jun, Chen, Richard, Dean, Shannon M, Decker, Antonio, DiPasquale, Thilo, Focken, Ivan, Hemeon, Kuldip, Khakh, Amy, Kim, Rainbow, Kwan, Andrea, Lindgren, Sophia, Lin, Jonathan, Maher, Janette, Mezeyova, Dinah, Misner, Karen, Nelkenbrecher, Jodie, Pang, Rebecca, Reese, Shannon D, Shields, Luis, Sojo, Tao, Sheng, Henry, Verschoof, Matthew, Waldbrook, Michael S, Wilson, Zhiwei, Xie, Clint, Young, Tanja S, Zabka, David H, Hackos, Daniel F, Ortwine, Andrew D, White, J P, Johnson, C Lee, Robinette, Christoph M, Dehnhardt, Charles J, Cohen, Daniel P, Sutherlin
Publikováno v:
Journal of medicinal chemistry. 64(6)
Na
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d744b2a5894fa87236be1caf92c75b8b
https://pubmed.ncbi.nlm.nih.gov/33682420
https://pubmed.ncbi.nlm.nih.gov/33682420
Autor:
Thilo, Focken, Sultan, Chowdhury, Alla, Zenova, Michael E, Grimwood, Christine, Chabot, Tao, Sheng, Ivan, Hemeon, Shannon M, Decker, Michael, Wilson, Paul, Bichler, Qi, Jia, Shaoyi, Sun, Clint, Young, Sophia, Lin, Samuel J, Goodchild, Noah G, Shuart, Elaine, Chang, Zhiwei, Xie, Bowen, Li, Kuldip, Khakh, Girish, Bankar, Matthew, Waldbrook, Rainbow, Kwan, Karen, Nelkenbrecher, Parisa, Karimi Tari, Navjot, Chahal, Luis, Sojo, C Lee, Robinette, Andrew D, White, Chien-An, Chen, Yi, Zhang, Jodie, Pang, Jae H, Chang, David H, Hackos, J P, Johnson, Charles J, Cohen, Daniel F, Ortwine, Daniel P, Sutherlin, Christoph M, Dehnhardt, Brian S, Safina
Publikováno v:
Journal of medicinal chemistry. 61(11)
The sodium channel Na
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::41b8d0a60c84d4f1a2c37587e6288037
https://pubmed.ncbi.nlm.nih.gov/29737846
https://pubmed.ncbi.nlm.nih.gov/29737846
Publikováno v:
Angewandte Chemie International Edition. 50:11798-11802
The [3 + 2] cycloaddition of (1,3) amphoteric aziridine aldehydes [released from dimers (I) and (VII)] with isocyanates provides access towards reduced aziridino-fused hydantoins (III) and (IX), resp., with three contiguous stereocenters.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0eb1ea8e954b968a6039e89cbad67fc5
https://doi.org/10.1002/anie.201106024
https://doi.org/10.1002/anie.201106024
Autor:
Zhi He, Shannon M. Decker, Brittany L. Inman, Takahito Kasahara, Naila Assem, Ryan Hili, Andrei K. Yudin
Publikováno v:
The Journal of organic chemistry. 77(13)
Unprotected aziridine aldehydes belong to the amphoteric class of molecules by virtue of their dual nucleophilicity/electrophilicity. The dimeric nature of these molecules, brought together by a weak and reversible aminal “connection”, was found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46b1995b5b74f789797228d8f6fe942f
https://pubmed.ncbi.nlm.nih.gov/22662756
https://pubmed.ncbi.nlm.nih.gov/22662756
Publikováno v:
ChemInform. 43
The [3 + 2] cycloaddition of (1,3) amphoteric aziridine aldehydes [released from dimers (I) and (VII)] with isocyanates provides access towards reduced aziridino-fused hydantoins (III) and (IX), resp., with three contiguous stereocenters.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ada0d3a9a74d2545cf97d05ce9486ad0
https://doi.org/10.1002/chin.201217128
https://doi.org/10.1002/chin.201217128
Publikováno v:
Tetrahedron Letters. 50:7286-7287
Herein, we describe the synthesis of 4,5-disubstituted-3-trihalomethylisothiazoles from trihaloacetonitriles and 2-cyanothioacetamides or 2-ethoxycarbonylthioacetamides. The reactivity of the necessary trihaloacetonitriles has a significant impact on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae3bacbf9c83297ded6472b277182bfe
https://doi.org/10.1016/j.tetlet.2009.10.051
https://doi.org/10.1016/j.tetlet.2009.10.051