Zobrazeno 1 - 10
of 293
pro vyhledávání: '"Allyl Sulfide"'
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Publikováno v:
The Journal of Organic Chemistry. 86:13598-13609
The heterogeneous gold(I)-catalyzed stereoselective thioallylation of electron-deficient alkynes with allyl sulfides has been achieved by using an MCM-41-immobilized sterically demanding NHC-gold(I) complex [MCM-41-IPrAuNTf2] as the catalyst under mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0f890a5156c656aaa8e977244a63204
https://doi.org/10.1021/acs.joc.1c01641
https://doi.org/10.1021/acs.joc.1c01641
Autor:
Jeffrey W. Stansbury, Xun Han, Xinpeng Zhang, Mingtao Chen, Parag K. Shah, Guangzhe Gao, Nancy Sowan, Christopher N. Bowman
Publikováno v:
ACS macro letters. 9(5)
Functional nanogels are attractive additives for use in polymer composites. In this study, nanogels with internal allyl sulfide moieties throughout their network structure were prepared via a thiol-Michael addition reaction. The excess thiol-function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf0b068c1be2249dc5362d387359dfb7
https://pubmed.ncbi.nlm.nih.gov/35648559
https://pubmed.ncbi.nlm.nih.gov/35648559
Publikováno v:
New Journal of Physics, Vol 21, Iss 4, p 045004 (2019)
Human mesenchymal stem cells (hMSCs) sense and respond to the bulk elastic and viscoelastic properties of their microenvironment, as well as the spatial distribution of these mechanical signals. Hydrogel substrates with photo-controlled mechanical pr
Externí odkaz:
https://doaj.org/article/2401027ad9284726813ac61f20900b0e
Publikováno v:
Chemistry-A European Journal, 27(1), 371-378. Wiley-VCH Verlag
Chemistry (Weinheim an Der Bergstrasse, Germany)
Chemistry (Weinheim an Der Bergstrasse, Germany)
The cobalt species PPh4[CoIII(TAMLred)] is a competent and stable catalyst for the sulfimidation of (aryl)(alkyl)‐substituted sulfides with iminoiodinanes, reaching turnover numbers up to 900 and turnover frequencies of 640 min−1 under mild and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6eb049d6308adcc01cc51a3adbc301a
https://doi.org/10.1002/chem.202003566
https://doi.org/10.1002/chem.202003566
Publikováno v:
Organic Chemistry Frontiers. 8:2990-2996
Allyl sulfides are important organosulfur compounds. K2S2O8 promoted dehydrative cross-coupling between α,α-disubstituted allylic alcohols and thiophenols/thiols is demonstrated for the first time, which resulted in a wide range of allyl sulfides i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f1b07045632b83910f5f47e9fd451e8
https://doi.org/10.1039/d1qo00148e
https://doi.org/10.1039/d1qo00148e
Publikováno v:
Organic Chemistry Frontiers. 8:6053-6062
The origin of chemoselectivity and the mechanism of the Au(I)-catalyzed [2,3]-sigmatropic rearrangement/cyclopropanation or C–H functionalization of diazoesters with allyl-functionalized sulfides, selenides, amines, or ethers as the second reactant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9393f41a5755ef9fbf93bdfda1e675f5
https://doi.org/10.1039/d1qo00920f
https://doi.org/10.1039/d1qo00920f
Publikováno v:
Organic Chemistry Frontiers. 8:6427-6432
A palladium catalyzed desulfurative coupling of allylthioethers with organoboronic acids under mild reaction conditions is described. The reaction exhibits high chemoselectivity and good functional group tolerance, allowing the synthesis of a wide ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfa4ef75fe9d261ed9974e43bcecce93
https://doi.org/10.1039/d1qo01106e
https://doi.org/10.1039/d1qo01106e
Akademický článek
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