Zobrazeno 1 - 10
of 80
pro vyhledávání: '"Anita E. Mattson"'
Autor:
Yong Guan, Tadas A. Buivydas, Remy F. Lalisse, Kalen B. Laybourn, Charlotte Stern, Margaret Richins, Sean M. Burns, Arielle Shelby, Christopher M. Hadad, Anita E. Mattson
Publikováno v:
ACS Catalysis. :7661-7668
Publikováno v:
Organic Letters. 25:2450-2455
Publikováno v:
Chemical Communications. 59:1241-1243
Correction for ‘Dearomatization of benzopyrylium triflates with sulfoxonium ylides’ by Alexandria N. Leveille et al., Chem. Commun., 2022, 58, 12600–12603, https://doi.org/10.1039/D2CC02023H.
Autor:
Anita E. Mattson, Yong Guan, Tadas Buivydas, Remy F. Lalisse, Rameez Ali, Christopher M. Hadad
Publikováno v:
Synthesis. 54:4210-4219
A catalytic and highly enantioselective dearomative alkynylation of chromanones has been discovered that enables the construction of biologically relevant tertiary ether stereogenic centers. This methodology is robust, accommodating a variety of alky
Publikováno v:
Anion‐Binding Catalysis. :201-220
Autor:
Jonathan W. Attard, Charlotte L. Stern, Yong Guan, Remy F. Lalisse, Anita E. Mattson, Christopher M. Hadad, Rameez Ali, Tadas A. Buivydas
Publikováno v:
ACS Catalysis. 11:6325-6333
Autor:
Matthew N. Grayson, Patrícia B. Momo, Antonio C. B. Burtoloso, Anita E. Mattson, Elliot H. E. Farrar, Alexandria N. Leveille
Publikováno v:
Angewandte Chemie (International Ed. in English)
Momo, P B, Leveille, A N, Farrar, E H E, Grayson, M N, Mattson, A E & Burtoloso, A C B 2020, ' Enantioselective S-H Insertion Reactions of α-Carbonyl Sulfoxonium Ylides ', Angewandte Chemie-International Edition, vol. 59, no. 36, pp. 15554-15559 . https://doi.org/10.1002/anie.202005563
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Momo, P B, Leveille, A N, Farrar, E H E, Grayson, M N, Mattson, A E & Burtoloso, A C B 2020, ' Enantioselective S-H Insertion Reactions of α-Carbonyl Sulfoxonium Ylides ', Angewandte Chemie-International Edition, vol. 59, no. 36, pp. 15554-15559 . https://doi.org/10.1002/anie.202005563
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
The first example of enantioselective S−H insertion reactions of sulfoxonium ylides is reported. Under the influence of thiourea catalysis, excellent levels of enantiocontrol (up to 95 % ee) and yields (up to 97 %) are achieved for 31 examples in S
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
The first example of organocatalytic enantioselective C-H insertion reactions of indoles and sulfoxonium ylides is reported. Under the influence of phosphoric acid catalysis, levels of enantiocontrol in the range of 20-93% ee and moderate yields (up
Autor:
Yong Guan, Sangram S. Parelkar, Alexandria N. Leveille, Paul R. Thompson, Elizabeth Vaughn, Anita E. Mattson, Rameez Ali
Publikováno v:
European J Org Chem
Select dimeric chromenones exhibit low micromolar cyctotoxicity toward lymphoma and leukemia cell lines, L5178Y and HL60, respectively. The bioactive dimeric chromenones were identified from a focused library of structurally-simplified derivatives of
Publikováno v:
Chemistry – A European Journal. 24:7123-7127
Silanediol and copper catalysis are merged, for the first time, to create an enhanced Lewis acid catalyst system for enantioselective heterocycle functionalization. The promise of this silanediol and copper catalyst combination is demonstrated in the