Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Shogo, Kamo"'
Publikováno v:
ACS Omega, Vol 5, Iss 42, Pp 27667-27674 (2020)
Externí odkaz:
https://doaj.org/article/dd6d23a2eb5a4e65b4aafa60a96292c7
Autor:
Kai Yoshioka, Shogo Kamo, Keisuke Hosaka, Ryohei Sato, Yuma Miikeda, Yuri Manabe, Shusuke Tomoshige, Kazunori Tsubaki, Kouji Kuramochi
Publikováno v:
ACS Omega, Vol 4, Iss 7, Pp 11737-11748 (2019)
Externí odkaz:
https://doaj.org/article/0eb74e867a7d43a8b684ea4956972414
Autor:
Kazuyuki Sugita, Eiji Nagata, Hisaaki Sakate, Takaharu Okada, Shinya Adachi, Shogo Kamo, Akinobu Matsuzawa
Publikováno v:
Synthesis. 55:663-669
In this article, we report the synthesis of (±)-5-epi-vetiverianine A. The key reactions, including a rhodium-catalyzed coupling reaction and an oxidative phenolic cyclization, allow for efficient and stereoselective access to (±)-5-epi-vetiveriani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7845c2bb8cbee4b92d9fd0759a5635df
https://doi.org/10.1055/a-1947-6049
https://doi.org/10.1055/a-1947-6049
Publikováno v:
Organic Chemistry Frontiers. 9:6849-6852
We describe the first total synthesis of (+)-ent-vetiverianine A, which exhibits a 5/6/6-fused tricyclic structure, with the longest linear sequence of 14 steps, and in 12% overall yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cec24688053b97d17de9607f4ab91d88
https://doi.org/10.1039/d2qo01525k
https://doi.org/10.1039/d2qo01525k
Autor:
Shinya Adachi, Kazuyuki Sugita, Tomoya Mashiko, Akinobu Matsuzawa, Shogo Kamo, Jun Sakai, Yuta Shingai
Publikováno v:
Angewandte Chemie. 133:24689-24692
Herein, we describe the first total synthesis of cochlearol B, a meroterpenoid natural product featuring a 4/5/6/6/6-fused pentacyclic structure. Key steps, oxidative cyclization and subsequent intramolecular [2+2] photocycloaddition, which construct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::940ffdca6fc5d8290eea7f192de26af9
https://doi.org/10.1002/ange.202110556
https://doi.org/10.1002/ange.202110556
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b51dde4e56995d649419e0c9608f176
https://doi.org/10.1002/ejoc.202201366
https://doi.org/10.1002/ejoc.202201366
Publikováno v:
Organicbiomolecular chemistry. 20(46)
In this study, we report the total syntheses of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e73bfb3241034bc24bfa157460c6505a
https://pubmed.ncbi.nlm.nih.gov/36373484
https://pubmed.ncbi.nlm.nih.gov/36373484
Publikováno v:
Synthesis. 53:2092-2102
In this paper, the synthesis of the carbon skeleton of cotylenin A aglycone is described. The key reactions, including an intramolecular aldol reaction, an aldol coupling reaction, and a ring-closing metathesis, allow for the effective and stereose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7848d1e8d102a2c8b5acd3acdc130f7b
https://doi.org/10.1055/s-0040-1706684
https://doi.org/10.1055/s-0040-1706684
Publikováno v:
Organic Chemistry Frontiers. 8:6063-6066
In this study, concise total syntheses of Peniclillium sesquiterpenes (±)-Penicibilaenes A and B are described. This approach involves an effective intramolecular aldol condensation to construct a bicyclic skeleton, a stereoselective rhodium-catalyz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb10c549dcfca7ee533c025c3b4d558b
https://doi.org/10.1039/d1qo01251g
https://doi.org/10.1039/d1qo01251g
Publikováno v:
Organic letters. 24(3)
In this study, we achieved an eight-step enantioselective synthesis of (-)-lamellodysidine A, a structurally intriguing sesquiterpene natural product featuring a 5/5/6/6-fused tetracyclic skeleton that was obtained from the marine sponge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::510fbeb30358e44330309a7d8769f2b1
https://pubmed.ncbi.nlm.nih.gov/35019657
https://pubmed.ncbi.nlm.nih.gov/35019657