Results 171 to 180 of about 37,076 (287)

EDA Complex–Mediated C(sp3)–H Cross‐Dehydrogenative Coupling Enables Synthesis of Noncanonical α,β‐Diamino Acids

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Access to nonproteinogenic α,β‐diamino acids from simple feedstock precursors is of great interest to generate medicinal small molecule libraries. We report a regioselective photoinduced C(sp3)–C(sp3) cross‐dehydrogenative coupling (CDC) of N‐arylglycine derivatives with amides.
Krishnakumar Sachidanandan   +4 more
wiley   +1 more source

Catalytic Enantioselective Cross-Nucleophile Coupling via Valence Tautomerism. [PDF]

open access: yesJ Am Chem Soc
Zhang Z   +8 more
europepmc   +1 more source

Synthesis of Phenanthryl Phenyl Ethers [PDF]

open access: yesBulletin of the Chemical Society of Japan, 1961
openaire   +1 more source

Catalytic Hydrogenation of Lignin‐Derived Aromatics With Rhodium Oxide in Water

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
The easily available, easy‐to‐handle rhodium(III) oxide, Rh2O3, is shown to be a competent catalyst for arene hydrogenation, including chemoselective reduction of α,β‐unsaturated aryl ketones. Catalytic arene hydrogenation offers a direct pathway to saturated carbocycles. It can also be exploited to upgrade lignin‐derived aromatics.
Zhenyu Chen   +8 more
wiley   +1 more source

Chan–Lam Cross‐Coupling With Alkylboron Reagents: From Transmetallation to Radical Pathways

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Alkylative Chan–Lam coupling overcomes intrinsic transmetallation limitations of alkylboron reagents by engaging radical pathways. Recent advances reveal how radical and radical–polar crossover mechanisms enable mild C(sp3)—heteroatom bond formation. This minireview highlights key mechanistic insights and emerging strategies that transform alkylboron ...
Nicolas G.‐Simonian   +3 more
wiley   +1 more source

Three-Way Chemodivergent Derivatization of Non-Activated 2-Arylphenyl Benzyl Ethers. [PDF]

open access: yesJ Org Chem
Solas M   +5 more
europepmc   +1 more source

Silyl Rearrangements in Gold‐Catalyzed Transformations

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
The synergy between the exceptional ability of gold catalysts to activate unsaturated substrates and the inherent tendency of organosilicon reagents to undergo silyl‐group rearrangements has unlocked a range of novel transformations, enabling access to otherwise challenging molecular architectures.
Patricia García‐Martínez   +1 more
wiley   +1 more source

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