Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Kevin G. M. Kou"'
Autor:
Yujie Cao, Kevin G. M. Kou
Publikováno v:
Handbook of CH-Functionalization. :1-39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01c40e1ba873f12d9c1beab7d4bc9642
https://doi.org/10.1002/9783527834242.chf0111
https://doi.org/10.1002/9783527834242.chf0111
Autor:
Aaron Pan, Maja Chojnacka, Robert Crowley, Lucas Göttemann, Brandon E. Haines, Kevin G. M. Kou
Publikováno v:
Chemical science, vol 13, iss 12
Dual Brønsted/Lewis acid catalysis involving environmentally benign, readily accessible protic acid and iron promotes site-selective tert-butylation of electron-rich arenes using di-tert-butylperoxide. This transformation inspired the development of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ededd34101fdb9c2cc55b6263c70418
https://escholarship.org/uc/item/5sj9v3qn
https://escholarship.org/uc/item/5sj9v3qn
Autor:
Kevin G. M. Kou, Xuezhen Kou
Publikováno v:
ACS Catalysis. 10:3103-3109
Carbon–hydrogen (C–H) bond functionalization streamlines synthesis by increasing step- and atom-economies. This approach, catalyzed by Rh(III), is combined with the α-arylation of ketone-derived si...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68df53ac76625e51a7430c1f9e8aca08
https://doi.org/10.1021/acscatal.9b05622
https://doi.org/10.1021/acscatal.9b05622
Autor:
Aaron, Pan, Maja, Chojnacka, Robert, Crowley, Lucas, Göttemann, Brandon E, Haines, Kevin G M, Kou
Publikováno v:
Chemical science. 13(12)
Dual Brønsted/Lewis acid catalysis involving environmentally benign, readily accessible protic acid and iron promotes site-selective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8a69cb8151b0f1ca751d913c5a604a32
https://pubmed.ncbi.nlm.nih.gov/35432882
https://pubmed.ncbi.nlm.nih.gov/35432882
Autor:
Kevin G. M. Kou, Viviene K. Nguyen
Publikováno v:
Organic & biomolecular chemistry, vol 19, iss 35
This mini-review provides a concise overview of the biosynthetic pathway and pharmacology of bisbenzylisoquinoline alkaloid (bisBIA) natural products. Additional emphasis is given to the methodologies in the total syntheses of both simpler acyclic di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae0a1ccc7973a4aea2dd7d1b3c7e721f
https://pubmed.ncbi.nlm.nih.gov/34524341
https://pubmed.ncbi.nlm.nih.gov/34524341
Autor:
Xuezhen Kou, Kevin G. M. Kou
Publikováno v:
ACS Catalysis. 11:11510-11510
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1669d0f4e19430e1a0275061557fc721
https://doi.org/10.1021/acscatal.1c03643
https://doi.org/10.1021/acscatal.1c03643
Autor:
Richmond Sarpong, Naomi Kelley, Danilo Pereira de Sant'Ana, Sven C. Richter, Eduardo V. Mercado-Marin, Yasuo Hirooka, Ken Mukai, David E. Stephens, Kevin G. M. Kou
Publikováno v:
Mukai, K; Sant'Ana, DPD; Hirooka, Y; Mercado-Marin, EV; Stephens, DE; Kou, KGM; et al.(2018). Bioinspired chemical synthesis of monomeric and dimeric stephacidin A congeners. Nature Chemistry, 10(1), 38-44. doi: 10.1038/NCHEM.2862. UC Riverside: Retrieved from: http://www.escholarship.org/uc/item/4zw0n9xz
Nature chemistry, vol 10, iss 1
Nature chemistry, vol 10, iss 1
© 2017 Macmillan Publishers Limited, part of Springer Nature. Stephacidin A and its congeners are a collection of secondary metabolites that possess intriguing structural motifs. They stem from unusual biosynthetic sequences that lead to the incorpo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c81aa9ab0274dca03f5bff875cc56f4c
https://doi.org/10.1038/nchem.2862
https://doi.org/10.1038/nchem.2862
Autor:
Nicolle A. Doering, Richmond Sarpong, Jack C. Lee, Christopher J. Marth, Gary M. Gallego, Kevin G. M. Kou, Krissada Norseeda
Publikováno v:
The Journal of organic chemistry, vol 83, iss 20
A copper-mediated conjugate addition of electron-rich aryl groups into a complex vinyl nitrile using arylmagnesium bromides is reported. The conjugate addition adducts were advanced toward the synthesis of designed aconitine-type analogues. The varia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6958662e399449a214c0194d64a97988
https://europepmc.org/articles/PMC6214151/
https://europepmc.org/articles/PMC6214151/
Publikováno v:
Organic Reactions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f7ec60fcb811d28a0e09373372aae95
https://doi.org/10.1002/0471264180.or096.02
https://doi.org/10.1002/0471264180.or096.02
Autor:
Vy M. Dong, Kevin G. M. Kou
Publikováno v:
Organic & Biomolecular Chemistry. 13:5844-5847
Sulfoxides are uncommon substrates for transition-metal catalysis due to their propensity to inhibit catalyst turnover. In a collaborative effort with Ken Houk, we developed the first dynamic kinetic resolution (DKR) of allylic sulfoxides using asymm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79996d05cadef12ac6ba39533c40393d
https://doi.org/10.1039/c5ob00083a
https://doi.org/10.1039/c5ob00083a