Results 181 to 190 of about 111,262 (332)
Thioxanthone: A Benchmark Photocatalyst for Organic Synthesis
Thioxanthone is a highly versatile and effective organocatalyst for photochemical applications, with its low‐toxicity, metal‐free structure driving growing interest in sustainable photocatalysis. Building on our previous 2021 review, this update covers advances from 2021–2025 in thioxanthone‐based synthetic organic photochemistry – excluding ...
Vera P. Demertzidou+2 more
wiley +1 more source
Malonic Acid Biosynthesis in Bush Bean Roots. II. Purification and Properties of Enzyme Catalyzing Oxidative Decarboxylation of Oxaloacetate [PDF]
Leland M. Shannon+2 more
openalex +1 more source
Electrochemical Borylation of C−C and C−Het Bonds
Electrosynthesis enables the cleavage and borylation of C−C, C−N, C−O, and C−S bonds, representing a significant advancement in organic chemistry. This approach offers a metal‐free strategy for synthesizing organoboron compounds, which find extensive applications across synthetic chemistry, biomedicine, and materials science.
Tsoh Lam Cheung, Hairong Lyu
wiley +1 more source
THE FORMATION OF TAURINE BY THE DECARBOXYLATION OF CYSTEIC ACID
Abraham White, Jacob B. Fishman
openalex +1 more source
The synergistic decarboxylation of glyoxylate and 2-oxoglutarate by an enzyme system from pig-liver mitochondria [PDF]
P. R. Stewart, J. R. Quayle
openalex +1 more source
Visible Light‐Induced N‐Heterocyclic Nitrenium‐Catalyzed Deoxygenative Borylation of Acyl Chlorides
Herein, direct deoxygenative borylation of acyl chlorides is reported, which is an unknown but desirable chemical transformation. The N‐heterocyclic nitrenium ion has been utilized as the photocatalyst under mild reaction conditions to synthesize a series of alkylboronates using bis‐(catecholato)diboron (B2cat2) as the diboron reagent.
Rahul Mondal+2 more
wiley +1 more source
Distant precursors of benzylisoquinoline alkaloids and their enzymatic formation [PDF]
Rüffer, Martina, Zenk, Meinhart H.
core +1 more source
Development of an Efficient Stereoretentive Para‐Claisen‐Cope Rearrangement
The stereoretentive para‐Claisen‐Cope rearrangement enabled by Europium catalysis is presented, achieving precise phenol functionalization with exceptional chirality transfer under air‐ and moisture‐tolerant conditions. A novel carbonate unlocks superior enantioselectivity in the Tsuji‐Trost allylic alkylation, paving the way for highly enantioenriched
Johanna Breinsperger+3 more
wiley +1 more source