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当分野において全合成を達成した化合物 (2009~2022)
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Org. Biomol. Chem., accepted for publication (2020), (DOI:10.1039/D2OB00274D) |
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Tetrahedron, 76, 131630 (2020) |
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Tetrahedron, 76, 131630 (2020) |
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Angew. Chem. Int. Ed., 59, 23089 (2020) |
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Org. Lett., 22, 6239 (2020) |
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Org. Lett., 22, 6239 (2020) |
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Org. Lett., 22, 6239 (2020) |
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-CC-1065.jpg) |
Org. Lett., 21, 6185-6189 (2019) |
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-lepadiformine A.jpg) |
Org. Lett., 22, 3313–3317 (2020) |
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Chem. Eur. J., accepted article (2020) |
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-castoramine.jpg) |
Synlett, 29, 1786-1790 (2018) |
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-pestalazine B.jpg) |
Org. Lett., 21, 4205–4209 (2019) |
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Org. Lett., 21, 3954–3958 (2019) |
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-epiamauromine.jpg) |
Org. Lett., 19, 5308–5311 (2017) |
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-novoamauromine.jpg) |
Org. Lett., 19, 5308–5311 (2017) |
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Angew. Chem. Int. Ed., 56, 12277-12281 (2017) |
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-Histrionicotoxin.jpg) |
Angew. Chem. Int. Ed., 56, 1087-1091 (2017) |
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J. Org. Chem., 82, 353-371 (2017) |
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-SCH 64874.jpg) |
J. Org. Chem., 82, 353-371 (2017) |
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Asian J. Org. Chem., 6, 54-58 (2017) |
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Asian J. Org. Chem., 6, 54-58 (2017) |
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J. Antibiot.,69, 253-258 (2016) |
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Adv. Synth. Catal., 358, 380-385 (2016) |
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-MPC1001B.jpg) |
Angew. Chem. Int. Ed., 55, 283-287 (2016) |
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-isoschizogamine .jpg) |
Chem. Eur. J., 21, 16400-16403 (2015) |
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-Indolactam V.jpg) |
Tetrahedron, 71, 3833-3837 (2015) |
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-Haouamine B.jpg) |
Angew. Chem. Int. Ed., 53, 13215–13219 (2014) |
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Org. Lett., 16, 2526–2529 (2014) Tetrahedron Lett., 79, 131809 (2020) |
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Org. Lett., 16, 2526–2529 (2014) Tetrahedron Lett., 79, 131809 (2020) |
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Org. Lett., 16, 2526–2529 (2014) |
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Tetrahedron, 69, 10946–10954 (2013)
Chem. Commun., 46, 2641–2643 (2010) |
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Tetrahedron, 69, 10946–10954 (2013)
Chem. Commun., 46, 2641–2643 (2010) |
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-Rhazinilam.jpg) |
Angew. Chem. Int. Ed., 52, 7168–7171 (2013)
Tetrahedron, 71, 3619-3624 (2015)
Tetrahedron Lett., 79, 131809 (2020) |
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-Rhazinicine.jpg) |
Angew. Chem. Int. Ed., 52, 7168–7171 (2013) |
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-Mersicarpine.jpg) |
Chem. Eur. J., 19, 9325–9334 (2013)
Org. Lett., 14, 2320–2322 (2012) |
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Org. Lett., 15, 1946–1949 (2013) |
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-Aspidophytine.jpg) |
Tetrahedron, 69, 89–95 (2013) |
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-Cimicidine.jpg) |
Tetrahedron, 69, 89–95 (2013)
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-Cimicine.jpg) |
Tetrahedron, 69, 89–95 (2013) |
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Angew. Chem. Int. Ed., 51, 13062–13065 (2012) |
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Tetrahedron, 68, 9376–9383 (2012) |
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Tetrahedron, 68, 9376–9383 (2012) |
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Tetrahedron, 68, 9376–9383 (2012) |
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Tetrahedron, 68, 9376–9383 (2012)
RSC Adv., 2, 5147-5149 (2012) |
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Tetrahedron, 68, 9376–9383 (2012) |
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Tetrahedron, 68, 9376–9383 (2012)
RSC Adv., 2, 5147-5149 (2012) |
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Chem. Asian J., 6, 560–572 (2011)
Angew. Chem. Int. Ed., 49, 5925–5929 (2010) |
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Chem. Asian J., 6, 560–572 (2011)
Angew. Chem. Int. Ed., 49, 5925–5929 (2010) |
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Chem. Asian J., 6, 560–572 (2011) |
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Chem. Asian J., 6, 560–572 (2011) |
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Chem. Asian J., 6, 560–572 (2011) |
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-Petrosin.jpg) |
Org. Lett., 12, 5196–5199 (2010) |
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Synlett, 822–826 (2010) |
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-Haplophytine.jpg) |
Angew. Chem. Int. Ed.,55, 15157–15161 (2016)
Angew. Chem. Int. Ed., 48, 7600–7603 (2009) |
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