Zobrazeno 1 - 10
of 72
pro vyhledávání: '"hypervalent iodine reagents"'
Autor:
Samata E. Shetgaonkar, Aleena Raju, Hideyasu China, Naoko Takenaga, Toshifumi Dohi, Fateh V. Singh
Publikováno v:
Frontiers in Chemistry, Vol 10 (2022)
Graphical Abstract
Externí odkaz:
https://doaj.org/article/dd13d846b273457fb3d3c2b46a3ddfe1
Publikováno v:
Molecules, Vol 27, Iss 12, p 3900 (2022)
The chemistry of polyvalent iodine compounds has piqued the interest of researchers due to their role as important and flexible reagents in synthetic organic chemistry, resulting in a broad variety of useful organic molecules. These chemicals have po
Externí odkaz:
https://doaj.org/article/3b2c47a979b64178a1e1214b901215f8
Autor:
Samata E. Shetgaonkar, Fateh V. Singh
Publikováno v:
Frontiers in Chemistry, Vol 8 (2020)
Hypervalent iodine compounds are valuable and versatile reagents in synthetic organic chemistry, generating a diverse array of useful organic molecules. Owing to their non-toxic and environmentally friendly features, these reagents find potential app
Externí odkaz:
https://doaj.org/article/0c4ebebb14214ef083183907205d7d12
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1778-1805 (2018)
Hypervalent iodine reagents have been developed as highly valuable reagents in synthetic organic chemistry during the past few decades. These reagents have been identified as key replacements of various toxic heavy metals in organic synthesis. Variou
Externí odkaz:
https://doaj.org/article/83c714e3d7d84ae883402fc88016ceea
Autor:
Le Du, Eliott Hugo Joran
Alkynes are found in a multitude of natural or synthetic bioactive compounds. In addition to the capacity of these chemical motifs to impact the physicochemical properties of a molecule of interest, the well-established reactivity of alkynes makes th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::336b06eec83e26535e282111f22210fa
Publikováno v:
Molecules, Vol 26, Iss 1, p 140 (2020)
Oxidative fragmentation of tertiary cyclopropanols with phenyliodine(III) dicarboxylates in aprotic solvents (dichloromethane, chloroform, toluene) produces mixed anhydrides. The fragmentation reaction is especially facile with phenyliodine(III) reag
Externí odkaz:
https://doaj.org/article/6926714d5dc24581be8ef8f851a6ca7e
Autor:
Nina Declas, Jerome Waser
Publikováno v:
Angewandte Chemie International Edition. 59:18256-18260
We report an Umpolung strategy of enol ethers to generate oxy-allyl cation equivalents based on the use of hypervalent iodine reagents. Under mild basic conditions, the addition of nucleophiles to aryloxy-substituted vinylbenziodoxolone (VBX) reagent
The goal of my PhD was the development of a new method for unselective surface labeling, not substrate-specific, that would give access to direct visualization of any surface interactions. In order to achieve this challenging goal, we wanted to devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d5ba449ea70dec697c2ea85ae2d2700
Publikováno v:
Molecules, Vol 23, Iss 5, p 1142 (2018)
Detailed investigations concerning the organocatalytic (asymmetric) α-azidation of prochiral β-ketoesters were carried out. It was shown that the racemic version of such a reaction can either be carried out under oxidative conditions using TMSN3 as
Externí odkaz:
https://doaj.org/article/379f86f973cc4b3ba38e9933d83bb3cf
Autor:
Wang, Chenyang
Publikováno v:
Aachen : RWTH Aachen University 1 Online-Ressource : Illustrationen (2021). doi:10.18154/RWTH-2021-08359 = Dissertation, RWTH Aachen University, 2021
Dissertation, RWTH Aachen University, 2021; Aachen : RWTH Aachen University 1 Online-Ressource : Illustrationen (2021). = Dissertation, RWTH Aachen University, 2021
Since 2016, the preparation and reactivity of sulfoximidoyl-containing hypervale
Since 2016, the preparation and reactivity of sulfoximidoyl-containing hypervale
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ed2d9c1c99fa3f7f2b90c23fc6193e7