Results 11 to 20 of about 19,002,772 (320)

Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis. [PDF]

open access: yesACS Catal, 2019
A weakly coordinating monodentate heteroaryl thioether directing group has been developed for use in Pd(II) catalysis to orchestrate key elementary steps in the catalytic cycle that require conformational flexibility in a manner that is difficult to ...
Romine AM   +4 more
europepmc   +12 more sources

Amine‐Catalyzed Copper‐Mediated C−H Sulfonylation of Benzaldehydes via a Transient Imine Directing Group** [PDF]

open access: yesAngewandte Chemie - International Edition, 2022
Transient directing groups (TDGs) can provide a powerful means for C–H functionalization without requiring additional steps for directing group introduction and removal.
Joe I Higham, James A Bull
exaly   +4 more sources

Directing-Group-Enabled Cycloaddition of Azides and Alkynes toward Functionalized Triazoles.

open access: yesOrganic Letters, 2020
Herein, we report a directing-group-enabled Huisgen cycloaddition of azides and alkynes for the synthesis of functionalized triazoles in which the triazene group could act as a directing group to enable this regioselective [3 + 2] cycloaddition and ...
Linwei Zeng   +4 more
semanticscholar   +2 more sources

Pd(II)-Catalyzed Synthesis of Benzocyclobutenes by β-Methylene-Selective C(sp3)-H Arylation with a Transient Directing Group.

open access: yesJournal of the American Chemical Society, 2021
Methylene-selective C-H functionalization is a significant hurdle that remains to be addressed in the field of Pd(II) catalysis. We report a Pd(II)-catalyzed synthesis of benzocyclobutenes by methylene-selective C(sp3)-H arylation of ketones.
Philip A Provencher   +6 more
semanticscholar   +2 more sources

Directing-Group-Assisted Manganese-Catalyzed Cyclopropanation of Indoles.

open access: yesOrganic Letters, 2019
The first manganese-catalyzed cyclopropanation of indoles is reported in moderate to excellent yield with methyl-2-diazo-2-arylacetates. This new strategy involved acetyl (COCH3) as the directing group and exhibited exceptional functional group tolerance.
P. K. Dutta   +3 more
semanticscholar   +3 more sources

A Transient Directing Group Strategy Enables Enantioselective Reductive Heck Hydroarylation of Alkenes

open access: yesAngewandte Chemie, 2019
Metal-coordinating directing groups have seen extensive use in the field of transition-metal-catalysed alkene functionalization; however, their waste-generating installation and removal steps limit the efficiency and practicality of reactions that rely ...
Lucas J. Oxtoby   +6 more
semanticscholar   +2 more sources

Stereospecific syn-dichlorination of allylic amines enabled by identification of a superior stereo-directing group [PDF]

open access: yesCommunications Chemistry
Alteration of a well-established reaction mechanism for access to different molecular structures is an inherently intriguing research subject. In that context, syn-stereospecific alkene dihalogenation draws attention as a long-standing problem in ...
Jeong Kyun Im   +2 more
doaj   +2 more sources

When is an Imine Directing Group a Transient Imine Directing Group in C-H Functionalization?

open access: yesChemistry
'Transient' C-H functionalization has emerged in recent years to describe the use of a dynamic linkage, often an imine, to direct cyclometalation and subsequent functionalization.
Joe I Higham, Tsz-Kan Ma, James A. Bull
semanticscholar   +2 more sources

Catalyst-controlled directing group translocation in the site selective C–H functionalization of 3-carboxamide indoles and metallocarbenes [PDF]

open access: yesNature Communications
Complementary methods toward the selective functionalization of indole and oxindole frameworks employing an alternative strategy in heteroaryl C–H functionalizations are presented herein.
Kuang Gu   +4 more
doaj   +2 more sources

Directing-Group-Free Arene C(sp2)-H Amination Using Bulky Aminium Radicals and DFT Analysis of Regioselectivity. [PDF]

open access: yesJ Org Chem, 2023
A hydroxylamine-derived electrophilic aminating reagent produces a transient and bulky aminium radical intermediate upon in situ activation by either TMSOTf or TFA and a subsequent electron transfer from an iron(II) catalyst.
Behnke NE   +4 more
europepmc   +3 more sources

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