Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Masanori, Nagatomo"'
Publikováno v:
Angewandte Chemie. 135
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c1766caee2a602e328e894bb3e7ecc8
https://doi.org/10.1002/ange.202219114
https://doi.org/10.1002/ange.202219114
Autor:
Maria Varghese, Masanori Nagatomo
Publikováno v:
Organic Syntheses. 98:491-508
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50569c63224e8e1559bfb1c289562bd4
https://doi.org/10.15227/orgsyn.098.0491
https://doi.org/10.15227/orgsyn.098.0491
Publikováno v:
The Journal of Organic Chemistry. 87:730-736
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::889ba4ba275cd4de5bd9efe86f430bcc
https://doi.org/10.1021/acs.joc.1c02736
https://doi.org/10.1021/acs.joc.1c02736
Publikováno v:
The Journal of Organic Chemistry. 86:16220-16230
Hikizimycin (1) is a potent anthelmintic and antibacterial natural product. The core 4-amino-4-deoxyundecose sugar (hikosamine) of 1 consists of an 11-carbon linear chain substituted with one amino group and 10 hydroxy groups. The C1 and C6O position
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8243c035d6b448a91fe39e2da274cdf6
https://doi.org/10.1021/acs.joc.1c01773
https://doi.org/10.1021/acs.joc.1c01773
Publikováno v:
Chemistry – An Asian Journal. 15:3820-3824
A newly devised radical-based strategy enabled coupling between multiply oxygenated α-alkoxyacyl tellurides and 2-hydroxybenzaldehyde derivatives. A reagent combination of Et3 B, Et2 AlCl, and O2 promoted the formation of the α-alkoxy carbon radica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a97aba12633f5b810dc3d6e3ce92768
https://doi.org/10.1002/asia.202001090
https://doi.org/10.1002/asia.202001090
Autor:
Yuki Kawashima, Takayuki Furukawa, Naoto Chatani, Mamoru Tobisu, Takumi Fukuda, Masanori Nagatomo, Masayuki Inoue
Publikováno v:
Organic Syntheses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21b673a1f2c3939ca2c3bd0f1d6bb5e1
https://doi.org/10.1002/0471264229.os096.03
https://doi.org/10.1002/0471264229.os096.03
Publikováno v:
Organic letters. 24(3)
Resiniferatoxin (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45879d69cb67aa3a2117b960e9d2f521
https://pubmed.ncbi.nlm.nih.gov/35043639
https://pubmed.ncbi.nlm.nih.gov/35043639
Autor:
Ben Greatrex, Masanori Nagatomo
Publikováno v:
Organic Syntheses. 97:38-53
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59afd266034ca8971629830ce81db899
https://doi.org/10.15227/orgsyn.097.0038
https://doi.org/10.15227/orgsyn.097.0038
Publikováno v:
Organic Letters. 21:7619-7623
A mild radical-based coupling method was devised for intermolecular installation of quaternary carbons. Treatment of α,α-dialkoxyacyl telluride with Et3B/O2 at room temperature promoted the formati...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f1c39df7b77ff0a3a21d8f6edeb1b06
https://doi.org/10.1021/acs.orglett.9b02895
https://doi.org/10.1021/acs.orglett.9b02895
Publikováno v:
Angewandte Chemie. 131:12287-12291
1-Hydroxytaxinine (1) is a cytotoxic taxane diterpenoid. Its central eight-membered B-ring possesses four oxygen-functionalized centers (C1, C2, C9, and C10) and two quaternary carbon centers (C8 and C15), and is fused with six-membered A- and C-ring
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75d9b7d5d39ba00281d587b5689fc447
https://doi.org/10.1002/ange.201906872
https://doi.org/10.1002/ange.201906872