Results 91 to 100 of about 3,554 (196)

Recent advances in polymeric chemically amplified positive resists: Materials and design strategies

open access: yesSmart Molecules, EarlyView.
This review summarizes recent advances in the molecular design of positive chemically amplified resists, focusing on photoacid generators and polymer architectures. Key strategies for enhancing sensitivity—including self‐amplification effects, copolymerization of sensitive monomers, controlled polymerization, and photosensitized chemically amplified ...
Litao Zhou   +3 more
wiley   +1 more source

Oxidative amidation of benzaldehydes and benzylamines withN-substituted formamides over a Co/Al hydrotalcite-derived catalyst

open access: yes, 2017
A highly efficient synthetic strategy for amidesviaoxidative amidation of benzaldehydes or benzylamines withN-substituted formamides has been developed using cobalt based heterogeneous catalyst.
Akhil V. Nakhate   +4 more
core   +1 more source

Surface Ligand Engineering in Quantum Dot Photocatalysis: Mechanisms, Design Principles, and Applications

open access: yesAdvanced Chemical Engineering, Volume 1, Issue 2, December 2026.
Surface ligands govern quantum dot photocatalysis through thermodynamic band‐edge tuning, kinetic charge‐transfer regulation, and microenvironmental control. Rational ligand engineering, using short‐chain, inorganic, conjugated, or dual‐ligand systems, enables efficient solar fuel production, selective organic transformations, environmental remediation,
Yali Weng   +5 more
wiley   +1 more source

Synthesis of Cyclic Sulfilimines and Sulfoximines via Copper‐Mediated C(sp2)–H Sulfanylation of Benzylamines with a Catalytic Transient Directing Group

open access: yesChemistryEurope
C─H functionalization presents opportunities to streamline the synthesis of valuable molecular structures. This study details the development of a copper‐mediated, transient C(sp2)–H sulfanylation of benzylamines with a transient directing group (TDG ...
Tsz‐Kan Ma   +4 more
doaj   +1 more source

Kinetic Resolution of Benzylamines via Palladium(II)-Catalyzed C–H Cross-Coupling

open access: yes, 2016
A Pd­(II)-catalyzed enantioselective C–H cross-coupling of benzylamines via kinetic resolution has been achieved using chiral mono-N-protected α-amino-O-methylhydroxamic acid (MPAHA) ligands.
Gang Chen (107840)   +3 more
core   +1 more source

Cholinesterases, carbonic anhydrase inhibitory properties and in silico studies of novel substituted benzylamines derived from dihydrochalcones

open access: yes, 2021
A series of novel urea, sulfamide and N,N-dipropargyl substituted benzylamines were synthesized from dihydrochalcones. The synthesized compounds were evaluated for their cholinesterases and carbonic anhydrase inhibitory actions.
Göksu, Süleyman   +12 more
core   +1 more source

Pyridine‐2‐Sulfinate as a Bifunctional SO2 Transfer Reagent; Unlocking Structurally Diverse, Ortho‐Functionalized Masked Sulfinates

open access: yesAdvanced Synthesis &Catalysis, Volume 368, Issue 21, 3 November 2026.
The commercially available 2‐pyridyl “Willis’ sulfinate” is demonstrated as an efficient SO2 transfer reagent (STR) providing single‐step access to a 2‐pyridyl masked sulfinate from (hetero)aryl bromides and iodides. Following installation, the pyridyl auxiliary delivers ortho‐selective functionalization via chelate‐assisted CH activation, providing a ...
Keegan McKibbon   +5 more
wiley   +1 more source

Three-Component Reaction of Benzylamines, Diethyl Phosphite and Triethyl Orthoformate: Dependence of the Reaction Course on the Structural Features of the Substrates and Reaction Conditions

open access: yesMolecules, 2017
The reaction between benzyl amines, triethyl orthoformate, and diethyl phosphite affords either bisphosphonic (compound 1) or N-benzylaminobenzylphosphonic (compound 2) acid depending on the reaction conditions.
Patrycja Miszczyk   +3 more
doaj   +1 more source

Reductive Amination with Zinc Borohydride. Efficient, Safe Route to Fluorinated Benzylamines

open access: yes, 1997
Fluorinated benzylamines are synthesized in high yields by reductive alkylation of secondary amines with appropriate fluoroaldehydes using a combination of zinc chloride and zinc borohydride.
Bhattacharyya, Sukanta   +2 more
core   +1 more source

Thiolane Sulfoximines as Azide Surrogates for Quinolyl Nitrenes: Photochemical Access to Ortho‐Diaminoquinolines

open access: yesAdvanced Synthesis &Catalysis, Volume 368, Issue 21, 3 November 2026.
Thiolane sulfoximines provide practical and safer surrogates for hazardous azides in nitrene photochemistry, enabling direct access to 7,8‐diaminoquinolines and fused δ‐lactams. DFT calculations support the reaction mechanism and rationalize product selectivity.
Lorenzo Serusi   +5 more
wiley   +1 more source

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