Results 91 to 100 of about 1,571 (154)

Substitutive Approach Toward Heteroaromatic Amino Alcohols Accessed Through Dioxolanyl Radical Linchpin. [PDF]

Adv Synth Catal
Chang JJ, Kumar M, Kashatus RC, Tomaselli DJ, Kim DK.   +4 more
europepmc   +1 more source

Stereoselective Synthesis and Functionalization of Acetylenic Boronic Esters. [PDF]

Org Lett
Schäfer P, Kazmaier U.
europepmc   +1 more source

Electrochemical deoxygenative trifluoromethylallenylation of propargylic alcohols <i>via</i> sodium-mediated pre-association. [PDF]

Chem Sci
Jang J, Kim H, Cho EJ.
europepmc   +1 more source

Copper-Catalyzed Three-Component Selective 1,4-Amino Oxygenation of 1,3-Dienes. [PDF]

Angew Chem Int Ed Engl
Feng G, Velopolcek MK, Wang Q.
europepmc   +1 more source

Photochemical carboborylation and three-component difunctionalization of α,β-unsaturated ketones with boronic acids via tosylhydrazones. [PDF]

Chem Sci
Valdés-Maqueda Á, Plaza M, Valdés C.
europepmc   +1 more source

Biomimetic Catalytic Remote Desaturation of Aliphatic Alcohols. [PDF]

Org Lett
Zuo K, Zhu J, Akhtar F, Dam P, Azofra LM, El-Sepelgy O.   +5 more
europepmc   +1 more source

2,6-Dioxabicyclo[3.3.1]nonan-3-ones: from natural product treasure troves to synthetic triumphs. [PDF]

RSC Adv
Choudhury UM, Das PP, Mohapatra DK.
europepmc   +1 more source

Catalytic Oxidative Ligand Transfer of Rh-Carbynoids and Alkyl Iodides. [PDF]

J Am Chem Soc
Esteve Guasch J, Pal D, Suero MG.
europepmc   +1 more source

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Nickel-Catalyzed Isomerization of Homoallylic Alcohols

Organic Letters, 2023
Nickel-catalyzed isomerizations of homoallylic alcohols and a bishomoallylic alcohol are presented. These isomerization reactions occur in the presence of a simple nickel catalyst that does not require addition of an exogenous ligand. The corresponding ketone products are generated in ≤98% yield.
Dustin D. Youmans, Hai N. Tran, Levi M. Stanley   +2 more
openaire   +2 more sources

Oxidation of homoallyl alcohols

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 1986
1. Parallel polymerization (10–20%) and oxidative-degradation (20–40%) reactions occur during oxidation of diallylcarbinol and related compounds to ketones. 2. The optimal oxidizing agents for diallylcarbinol are chromic acid in a two-phase system, moist PCC, and DMSO/PBr3.
I. A. Korshevets, E. A. Mistryukov
openaire   +1 more source