Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Cheyenne S. Brindle"'
Autor:
Nicholas G. Boekell, Dana J. Cerone, Maria M. Boucher, Phong K. Quach, Wilfried B. Tentchou Nganyak, Christine G. Reavis, Ifeanyi I. Okoh, Jordan O. A. Reid, Hayley E. Berg, Briana A. Chang, Cheyenne S. Brindle
Publikováno v:
SynOpen, Vol 01, Iss 01, Pp 0097-0102 (2017)
Abstract Triarylmethyl cations serve as tunable organocatalysts for the synthesis of bisindolylmethanes. The catalyst structure can be modified to increase or decrease reactivity as needed to match the requirements of the substrate. High yields are a
Externí odkaz:
https://doaj.org/article/f559b9db0ad541cd9af1209abc2f8b14
Autor:
Vanessa A. Jones, Kelly Lucas, Zhenghua Chen, Cheyenne S. Brindle, William J. Patterson, Kevin Bardelski, Melissa Guarino-Hotz
Publikováno v:
European Journal of Organic Chemistry. 2021:6737-6742
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa26972ce0bdf5cf8fea07b66af44e76
https://doi.org/10.1002/ejoc.202100946
https://doi.org/10.1002/ejoc.202100946
Publikováno v:
Organic Process Research & Development. 21:1394-1403
The reaction of the bisulfite ion with aldehydes to form charged bisulfite adducts is a well-established method for the purification of aldehydes. This reaction has been modified to create a convenient liquid–liquid extraction method for the remova
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e60a335a3896e3843c03e6f65d42d084
https://doi.org/10.1021/acs.oprd.7b00231
https://doi.org/10.1021/acs.oprd.7b00231
Autor:
Wilfried B. Tentchou Nganyak, Maria M. Boucher, Jordan O. A. Reid, Nicholas G. Boekell, Briana A. Chang, Cheyenne S. Brindle, Hayley E. Berg, Phong K. Quach, Ifeanyi I. Okoh, Christine G. Reavis, Dana J. Cerone
Publikováno v:
SynOpen, Vol 01, Iss 01, Pp 0097-0102 (2017)
Triarylmethyl cations serve as tunable organocatalysts for the synthesis of bisindolylmethanes. The catalyst structure can be modified to increase or decrease reactivity as needed to match the requirements of the substrate. High yields are achieved f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6674f99527f3e5dd62216c2c94bc9393
http://www.thieme-connect.de/DOI/DOI?10.1055/s-0036-1588559
http://www.thieme-connect.de/DOI/DOI?10.1055/s-0036-1588559
Publikováno v:
Journal of Visualized Experiments.
The purification of organic compounds is an essential component of routine synthetic operations. The ability to remove contaminants into an aqueous layer by generating a charged structure provides an opportunity to use extraction as a simple purifica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b780969f13dbec04063f348acaf034a
https://doi.org/10.3791/57639-v
https://doi.org/10.3791/57639-v
Publikováno v:
Chemical reviews. 116(24)
Fostriecin and related natural products present a significant challenge for synthetic chemists due to their structural complexity and chemical sensitivity. This review will chronicle the successful efforts of synthetic chemists in the construction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3a98c30926d024679350ce687fe2af7
https://pubmed.ncbi.nlm.nih.gov/28027648
https://pubmed.ncbi.nlm.nih.gov/28027648
Autor:
Ming-Yu Ngai, Thomas J. Hunter, Cheyenne S. Brindle, Berenger Biannic, B. Michael O’Keefe, Barry M. Trost
Publikováno v:
Journal of the American Chemical Society
Leustroducsin B exhibits a large variety of biological activities and unique structural features. An efficient and highly convergent total synthesis of Leustroducsin B was achieved in 17 longest linear and 39 total steps by disconnecting the molecule
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9755aa30e5ba4b23b92e599050a1cee5
https://pubmed.ncbi.nlm.nih.gov/26313159
https://pubmed.ncbi.nlm.nih.gov/26313159
Publikováno v:
Chemical sciences journal. 4(5)
Highly enantioselective vicinal iodoamination of olefins is accomplished through the iodocyclization of alkenyl trichloroacetimidates catalysed by a new chiral Schiff-base urea derivative. The resulting products are converted readily to a variety of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31f2dc7d86521183935ba27e9b09de7b
https://pubmed.ncbi.nlm.nih.gov/24416631
https://pubmed.ncbi.nlm.nih.gov/24416631
Publikováno v:
ChemInform. 43
This article describes chemoselective and atom-economical methods for the stereoselective assembly of the A- and B-ring subunits of the bryostatins. A Ru-catalyzed tandem alkene-alkyne coupling/Michael addition was developed and applied to the synthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f71fca86c32a33974a4629b3b976594
https://doi.org/10.1002/chin.201201188
https://doi.org/10.1002/chin.201201188
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 17(35)
This article describes chemoselective and atom-economic methods for the stereoselective assembly of the ring A and B subunits of bryostatins. A Ru-catalyzed tandem alkene-alkyne coupling/Michael addition reaction was developed and applied to the synt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29bf63b6bd3a55742c628efb9a359a0d
https://pubmed.ncbi.nlm.nih.gov/21774000
https://pubmed.ncbi.nlm.nih.gov/21774000