Zobrazeno 1 - 10
of 111
pro vyhledávání: '"Nigel T. Lucas"'
Publikováno v:
Inorganic Chemistry. 62:5054-5057
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::567f4916b12d3ddcad06c18cf101cac2
https://doi.org/10.1021/acs.inorgchem.3c00198
https://doi.org/10.1021/acs.inorgchem.3c00198
Publikováno v:
ACS Catalysis. 13:3153-3157
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20cac5ade0eb72078810c73e9af048cc
https://doi.org/10.1021/acscatal.2c05657
https://doi.org/10.1021/acscatal.2c05657
Autor:
David Rubin, Catherine E. Sansom, David J. Richards, Nigel T. Lucas, Anna L. Garden, Patricio R. Saldivia Pérez, Janice M. Lord, Nigel B. Perry
Publikováno v:
Journal of Natural Products. 85:1893-1903
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31e854e9d08d405622500586897ead22
https://doi.org/10.1021/acs.jnatprod.2c00206
https://doi.org/10.1021/acs.jnatprod.2c00206
Autor:
David Rubin, Catherine E. Sansom, Nigel T. Lucas, C. John McAdam, Jim Simpson, Janice M. Lord, Nigel B. Perry
Publikováno v:
Journal of Natural Products. 85:1904-1911
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51e1d700a5bbb61e20a90c9e5c917461
https://doi.org/10.1021/acs.jnatprod.2c00207
https://doi.org/10.1021/acs.jnatprod.2c00207
Autor:
Wesley J. Olivier, Jason A. Smith, Alireza Ariafard, Alex C. Bissember, Nigel T. Lucas, Rasool Babaahmadi
Publikováno v:
Organic Letters. 23:8494-8498
This report investigates the fundamental basis for rather surprising patterns of reactivity in Bronsted acid-mediated cyclizations of pyrrole substrates bearing pendant Michael acceptors that were identified during syntheses of Stemona alkaloids. Int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4500f2e352fa782382399a8233312f41
https://doi.org/10.1021/acs.orglett.1c03205
https://doi.org/10.1021/acs.orglett.1c03205
Publikováno v:
Chemical Science
The octol of a new rigid, tetraarylene-bridged cavitand was investigated for self-assembly behaviour in solution. 1H and DOSY NMR spectroscopic experiments show that the cavitand readily dimerizes through an unusual seam of interdigitated hydrogen-bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48e95f3bfc94fb401052c4e4b627d227
http://europepmc.org/articles/PMC8442710
http://europepmc.org/articles/PMC8442710
Publikováno v:
Angewandte Chemie International Edition. 60:14897-14901
Palladium(II) boronates are recognized as fundamental pre-transmetalation intermediates in Suzuki-Miyaura cross-couplings. While these typically transient species have been detected and studied spectroscopically, it is conspicuous that they have neve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01ff36334a0fab472365b7bbf8311466
https://doi.org/10.1002/anie.202104802
https://doi.org/10.1002/anie.202104802
Autor:
Rebecca O. Fuller, Alex C. Bissember, Angus Olding, Curtis C. Ho, Allan J. Canty, Nigel T. Lucas
Publikováno v:
Organometallics. 40:2305-2310
This study investigates the mechanism of Suzuki-Miyaura Csp2-Csp2 cross-couplings facilitated by PCP-type nickel(II) pincer complexes. By employing a combination of standard experimental and theoretical methods, it is proposed that a nickel(I)/(III)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f953bef1a96c8c4b5a5ecf3068f165e3
https://doi.org/10.1021/acs.organomet.1c00033
https://doi.org/10.1021/acs.organomet.1c00033
Publikováno v:
The Journal of Organic Chemistry. 85:4574-4580
The three-component reaction between a resorcinol, 1,3-dimethoxybenzene, and an alkyl aldehyde (R = C1-C11) along with BF3·OEt2 affords a C2v-symmetric resorcin[4]arene tetraether in one step; in most cases, the single isomer can be precipitated fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8542c22c457b3c5d5f64d3f9fdb43588
https://doi.org/10.1021/acs.joc.0c00128
https://doi.org/10.1021/acs.joc.0c00128
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 27(62)
The first total syntheses of the Stemona alkaloid dehydrostenine A and the structure assigned to dehydrostenine B have been completed from a simple pyrrole substrate in 10 and 11 steps, respectively. Two independent Bronsted-acid-mediated intramolecu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28e9c9913580a4496519448388eb42a9
https://pubmed.ncbi.nlm.nih.gov/34426989
https://pubmed.ncbi.nlm.nih.gov/34426989