Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Junpei, Matsuoka"'
Autor:
Yuta Fujiki, Hiyono Suzuki, Junya Kikuzawa, Keiji Nishiwaki, Norihito Kawashita, Junpei Matsuoka, Akira Nakamura, Tomohiro Maegawa, Akiko Kuwabara, Masafumi Kobayashi, Kouichi Matsumoto
Publikováno v:
Chemistry Letters; Jun2024, Vol. 53 Issue 6, p1-5, 5p
Publikováno v:
Organic Letters. 24:9447-9451
A method for the synthesis of cyclic amides via phosphazene base-catalyzed intramolecular hydroamidation of amide alkenes was developed. The reaction using a catalytic amount of P4-base had a good functional group tolerance and a broad substrate scop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10c9146aaf000efa62bed2de30b8a7e1
https://doi.org/10.1021/acs.orglett.2c03870
https://doi.org/10.1021/acs.orglett.2c03870
Publikováno v:
The Chemical Record. 21:3897-3910
The exploitation of nitrogen-functionalized reactive intermediates plays an important role in the synthesis of biologically relevant scaffolds in the field of pharmaceutical sciences. Those based on gold carbenes carry a strong potential for the desi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aef4e0e0fe92989aee67492423fdaed7
https://doi.org/10.1002/tcr.202100202
https://doi.org/10.1002/tcr.202100202
Autor:
Junpei Matsuoka
Publikováno v:
YAKUGAKU ZASSHI. 140:1313-1322
In total and formal syntheses of dictyodendrins A, B, C, D, E and F, the key step involved the direct construction of the pyrrolo[2,3-c]carbazole core by the gold-catalyzed annulation of a conjugated diyne with a pyrrole to form three bonds and two a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9689991bc360a1c09361262322c9a0ab
https://doi.org/10.1248/yakushi.20-00162
https://doi.org/10.1248/yakushi.20-00162
Publikováno v:
Journal of Organic Chemistry. 84(14):9358-9363
We achieved direct construction of the common pyrrolo[2, 3-d]carbazole core of aspidosperma and malagasy alkaloids by a gold-catalyzed cascade cyclization of ynamide. This reaction involves intramolecular cyclization from indole to ynamide followed b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9885c3b20401dd89cb0cf930c783cd4a
http://hdl.handle.net/2433/243213
http://hdl.handle.net/2433/243213
Autor:
Masahiro Oka, Shinsuke Inuki, Yuka Matsuda, Hiroaki Ohno, Shinya Oishi, Junpei Matsuoka, Yoichi Miyamoto, Mayumi Otani
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 26(49)
The total synthesis of dictyodendrins A-F was achieved by using the gold(I)-catalyzed annulation of a conjugated diyne with N-Boc-pyrrole for direct construction of the pyrrolo[2,3-c]carbazole scaffold. Late-stage functionalization of the resulting p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9684a35741071c0b45c648def0eb238a
https://pubmed.ncbi.nlm.nih.gov/32364649
https://pubmed.ncbi.nlm.nih.gov/32364649
Autor:
Junpei Matsuoka
Publikováno v:
Springer Theses ISBN: 9789811586514
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29c912d90850d94009bc54a4a004d3ec
https://doi.org/10.1007/978-981-15-8652-1
https://doi.org/10.1007/978-981-15-8652-1
Autor:
Junpei Matsuoka
Publikováno v:
Total Synthesis of Indole Alkaloids ISBN: 9789811586514
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10517a71ac5d7ee786cf5f86b66aef52
https://doi.org/10.1007/978-981-15-8652-1_3
https://doi.org/10.1007/978-981-15-8652-1_3
Autor:
Junpei Matsuoka
Publikováno v:
Total Synthesis of Indole Alkaloids ISBN: 9789811586514
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62edc57bee2e39f0157b232fd1c0bc1a
https://doi.org/10.1007/978-981-15-8652-1_1
https://doi.org/10.1007/978-981-15-8652-1_1
Autor:
Junpei Matsuoka
Publikováno v:
Total Synthesis of Indole Alkaloids ISBN: 9789811586514
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b7a8badec9179d78274f725c195d068
https://doi.org/10.1007/978-981-15-8652-1_4
https://doi.org/10.1007/978-981-15-8652-1_4