Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Sunewang Rixin Wang"'
Autor:
Torsten Thiess, Alexander Hofmann, Dominic Prieschl, Sunewang Rixin Wang, Tobias Brückner, Thomas Kupfer, Rian D. Dewhurst, Holger Braunschweig, A. Gackstatter, Annalena Gärtner, Andrea Deißenberger
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 23(40)
Dihalodiboranes(4) react with a N-heterocyclic silylene (NHSi) to generate NHSi adducts of 1-aryl-2-silyl-1,2-diboraindanes, as was confirmed by X-ray crystallography, featuring the functionalization of both B-X (X=halogen) bonds and a sp3 - or sp2 -
Autor:
Merle Arrowsmith, Sunewang Rixin Wang, Holger Braunschweig, Lena Winner, Rian D. Dewhurst, Valerie Paprocki
Publikováno v:
Chem. Commun.
Upon complexation to CuOTf, a PMe\(_3\)-stabilized bis(9-anthryl) diborene slowly undergoes an intramolecular hydroarylation reaction at room temperature. Subsequent triflation of the B–H bond with CuOTf, followed by a PMe\(_3\) transfer, finally y
Autor:
Sunewang Rixin Wang, Zuowei Xie
Publikováno v:
Tetrahedron. 68:5269-5278
Reaction of carboryne generated from 1-I-2-Li-1,2-C2B10H10 with styrene and its derivatives has been studied. In addition to [2+2] cycloaddition reaction and/or ene reaction, an extra-annular [4+2] cycloaddition reaction is also observed, depending u
Autor:
Zuowei Xie, Sunewang Rixin Wang
Publikováno v:
Organometallics. 31:4544-4550
Insertion of o-carborynes (1,2-dehydro-o-carboranes) into ferrocenyl C–H bonds has been described, providing a convenient methodology for the preparation of functionalized ferrocenyl o-carboranes. Reaction of the carboryne precursors 1-I-2-Li-9,12-
Autor:
Sunewang Rixin Wang, Zuowei Xie
Publikováno v:
Organometallics. 31:3316-3323
Carboryne (1,2-dehydro-o-carborane), in situ generated from the precursor 1-iodo-2-lithiocarborane, reacted with alkylbenzenes to give two regioisomers of the [4 + 2] cycloadducts as the major products in moderate to good yields, in which the steric
Publikováno v:
ChemInform. 46
A commercial phosphorus-based reagent (P(NMe2)3) mediates umpolung alkylation of methyl aroylformates with benzylic and allylic bromides, leading to either Barbier-type addition or ylide-free olefination products upon workup. The reaction sequence is
A commercial phosphorus-based reagent (P-(NMe2)3) mediates umpolung alkylation of methyl aroylformates with benzylic and allylic bromides, leading to either Barbier-type addition or ylide-free olefination products upon workup. The reaction sequence i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d5af3208e01b427d4228e8353e55ef3
https://europepmc.org/articles/PMC4769642/
https://europepmc.org/articles/PMC4769642/
Publikováno v:
ChemInform. 44
A P(III)-mediated trimerization of unsaturated keto esters to diverse oxygenated heterocycles is reported.
Publikováno v:
Organic letters. 15(8)
A reductive homocondensation of E-benzylidenepyruvate esters mediated by P(NMe2)3 is described. The transformation, initiated by the Kukhtin–Ramirez addition of the phosphorus reagent to the vinyl-substituted α-dicarbonyl substrate, proceeds via a
Publikováno v:
Organic Letters; Vol. 15 Issue 8, p1926-1929, 4p