Results 101 to 110 of about 619,568 (137)

Base-Catalyzed Remote Hydrogermylation of Olefins. [PDF]

open access: yesAngew Chem Int Ed Engl
Ahrweiler E, Selmani A, Schoenebeck F.
europepmc   +1 more source

Direct vicinal halo-nitration of unsaturated compounds: an overview. [PDF]

open access: yesRSC Adv
Azizi Z   +8 more
europepmc   +1 more source

Unlocking the Aromatic Profile of Wild-Grown Croatian Fennel: A Comparative Study of Essential Oils and Hydrolates. [PDF]

open access: yesMolecules
Vučak A   +5 more
europepmc   +1 more source

1,2-Migratory ring expansion of a BN-naphthalene.

open access: yesOrg Biomol Chem
Mediavilla BA, Siegler MA, Klausen RS.
europepmc   +1 more source

Rhodium-Catalyzed β-Acylalkylation of Allylbenzene Derivatives with Allyl Alcohols via C–C Bond Cleavage

open access: yesJournal of Organic Chemistry, 2023
We report here a deallylative β-acylalkylation reaction of allylbenzene derivatives with allyl alcohols in the presence of Cp*Rh catalysts. Allylbenzenes possessing pyridyl and pyrazolyl directing groups were converted to β-aryl ketones via the cleavage of C(aryl)-C(allyl) bonds.
Takuya Kochi, Fumitoshi Kakiuchi
exaly   +4 more sources

Synthesis of Allylbenzene Derivatives through sp3 C–H Bond Functionalization of Toluene Derivatives

open access: yesSynlett, 2017
An sp3 C–H bond-transformation reaction of toluene substrates to afford the corresponding allylbenzene derivatives is described. Optimum conditions were identified as involving the use of tetrabutylammonium iodide and tert-butyl hydroperoxide at 80 °C.
Alireza Abbasi   +1 more
exaly   +3 more sources

Regioselective Cp*Ir(III)-Catalyzed Allylic C–H Sulfamidation of Allylbenzene Derivatives

open access: yesJournal of Organic Chemistry, 2019
In this study we report the development of the regioselective Cp*Ir(III)-catalyzed allylic C-H sulfamidation of allylbenzene derivatives, using azides as the nitrogen source. The reaction putatively proceeds through a Cp*Ir(III)-π-allyl intermediate and demonstrates exclusive regioselectivity for the branched position of the π-allyl.
Simon B Blakey   +2 more
exaly   +4 more sources

Cross‐Metathesis/Isomerization/Allylboration Sequence for a Diastereoselective Synthesis of Anti‐Homoallylic Alcohols from Allylbenzene Derivatives and Aldehydes

open access: yesChemistry – A European Journal, 2014
AbstractWe describe a highly diastereoselective approach to anti‐homoallylic alcohols from allylbenzene derivatives and aldehydes. The strategy is based on a cross‐metathesis/isomerization/allylboration sequence catalyzed successively by ruthenium and iridium.
Hemelaere, Rémy   +2 more
core   +4 more sources

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