Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.tetlet.2004.10.146
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dc.titleSynthetic studies towards anti-SARS agents: Application of an indium-mediated allylation of α-aminoaldehydes as the key step towards an intermediate
dc.contributor.authorChng, S.-S.
dc.contributor.authorHoang, T.-G.
dc.contributor.authorWayne Lee, W.-W.
dc.contributor.authorTham, M.-P.
dc.contributor.authorLing, H.Y.
dc.contributor.authorLoh, T.-P.
dc.date.accessioned2014-10-16T08:44:50Z
dc.date.available2014-10-16T08:44:50Z
dc.date.issued2004-12-20
dc.identifier.citationChng, S.-S., Hoang, T.-G., Wayne Lee, W.-W., Tham, M.-P., Ling, H.Y., Loh, T.-P. (2004-12-20). Synthetic studies towards anti-SARS agents: Application of an indium-mediated allylation of α-aminoaldehydes as the key step towards an intermediate. Tetrahedron Letters 45 (52) : 9501-9504. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tetlet.2004.10.146
dc.identifier.issn00404039
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/95185
dc.description.abstractAG7088 was identified as a good starting point for modification, leading to an efficient and bio-available inhibitor for the SARS coronavirus main proteinase (SARS-CoV M pro). Synthesis of intermediate 1 and analogues proceeded via a highly diastereoselective indium-mediated allylation of α-aminoaldehydes. © 2004 Elsevier Ltd. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.tetlet.2004.10.146
dc.sourceScopus
dc.subjectAG7088
dc.subjectAnti-SARS agents
dc.subjectDiastereoselective
dc.subjectIndium-mediated allylation
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/j.tetlet.2004.10.146
dc.description.sourcetitleTetrahedron Letters
dc.description.volume45
dc.description.issue52
dc.description.page9501-9504
dc.description.codenTELEA
dc.identifier.isiut000225623200001
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