Zobrazeno 1 - 10
of 135
pro vyhledávání: '"Eric M. Ferreira"'
Publikováno v:
Organic letters. 24(27)
Two strategies are described en route to an enantioselective total synthesis of gelsenicine. One approach centers on a chirality transfer cycloisomerization that ultimately fell short. Separately, an asymmetric catalysis route utilizing bisphosphine-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3206f2dc9af6320826f1ac20e47c052d
https://pubmed.ncbi.nlm.nih.gov/35796493
https://pubmed.ncbi.nlm.nih.gov/35796493
Autor:
Brian J. Knight, Eric M. Ferreira
Publikováno v:
Handbook of CH‐Functionalization. :1-26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ac6270590bf6aaf67b8b01e22ca98d5
https://doi.org/10.1002/9783527834242.chf0002
https://doi.org/10.1002/9783527834242.chf0002
Publikováno v:
Angewandte Chemie International Edition. 61
A direct dearomative photocatalyzed (3+2) cycloaddition between indoles and vinyldiazo reagents is described. The transformation is enabled by the development of a novel oxidizing Cr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1e7ff47b799940b720d9331cdc64cb4
https://doi.org/10.1002/anie.202212187
https://doi.org/10.1002/anie.202212187
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 28(62)
A synthesis of a δ-ketohydroperoxide is described, addressing potential functional-group compatibilities in these elusive species relevant to combustion and atmospheric chemistries. The hydroperoxide is installed via sulfonylhydrazine substitution,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d44dc138d68c114dd5021fa075446d9d
https://pubmed.ncbi.nlm.nih.gov/35945143
https://pubmed.ncbi.nlm.nih.gov/35945143
Publikováno v:
Tetrahedron. 134:133278
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63378ef82185132c8e465eb905405bb1
https://doi.org/10.1016/j.tet.2023.133278
https://doi.org/10.1016/j.tet.2023.133278
Autor:
Jeff P. Costello, Eric M. Ferreira
Publikováno v:
Org Lett
The steric and electronic drivers of regioselectivity in platinum-catalyzed intramolecular hydroalkoxylation are elucidated. A branch point is found that divides the process between 5-exo and 6-endo selective processes, and enol ethers can be accesse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::310afaca2298b9544b0e66c4eb1d02e8
https://doi.org/10.1021/acs.orglett.9b03557
https://doi.org/10.1021/acs.orglett.9b03557
Publikováno v:
Strategies and Tactics in Organic Synthesis ISBN: 9780128222126
The first total synthesis of (±)-gelsenicine is described. The strategy centers on a pivotal metal-catalyzed cycloisomerization–Cope rearrangement sequence to construct the central core of the Gelsemium alkaloid. The study provided a stimulating f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07d990cc1a1315d1de5233925078bffc
https://doi.org/10.1016/b978-0-12-822212-6.00005-9
https://doi.org/10.1016/b978-0-12-822212-6.00005-9
Publikováno v:
Angewandte Chemie International Edition. 57:11015-11019
A direct (3+2) cycloaddition between alkenes and vinyl diazo reagents using Cr or Ru photocatalysis is described. The intermediacy of a radical cation species enables a nucleophilic interception by vinyl diazo compounds, a departure from their tradit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24765827bef1902a880e53ffa8c1e993
https://doi.org/10.1002/anie.201805732
https://doi.org/10.1002/anie.201805732
Autor:
T. O. de Lima, S. N. dos Santos‐Araujo, A. de A. Lino, Luis Aurelio Sanches, L. C. de Araujo, P. K. Tomaz, Eric M. Ferreira
Publikováno v:
Grass and Forage Science. 73:588-598
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be7e7447a9128885d513efbb0825637a
https://doi.org/10.1111/gfs.12349
https://doi.org/10.1111/gfs.12349
Autor:
Curtis A. Seizert, Eric M. Ferreira
Publikováno v:
Tetrahedron. 73:4186-4194
A synthetic approach to pordamacrine A that features two key transformations is discussed. The first transformation applies an Ireland-Claisen rearrangement to establish sterically congested vicinal carbon centers. Although a hard enolization techniq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::310db103f3a0e6e1be6f9aa167028c75
https://doi.org/10.1016/j.tet.2016.11.030
https://doi.org/10.1016/j.tet.2016.11.030