Results 201 to 210 of about 24,726 (277)
Pseudotetraivprolide is a new player among the Detoxin/Rimosamide‐like natural products! Its biosynthesis requires FabD from primary metabolism and a PipDFG complex for final‐step acetylation – unlocking its anti‐antibotic activity. Abstract Novel variants of known natural product (NP) classes can provide valuable insights into their biosynthesis ...
Edna Bode +13 more
wiley +1 more source
We report herein the development of catalytic asymmetric synthesis of secondary alkyl boronates. Under the optimal conditions, Cu‐catalyzed semi‐reduction of 1‐alkyl‐ or 1,3‐dialkyl‐substituted 1‐boryl‐1,3‐butadienes forms secondary alkyl boronates with excellent regioselectivities and enantioselectivities.
Wen‐Bin Cao +5 more
wiley +2 more sources
All-Heteroatom-Substituted Carbon Spiro Stereocenters: Synthesis, Resolution, Enantiomeric Stability, and Absolute Configuration. [PDF]
Viudes O +6 more
europepmc +1 more source
Rearrangement of Protected Epoxy-Alcohols into Tetrahydrofuran Derivatives: The Protecting Group Matters! [PDF]
Nirpal AK, Sathyamoorthi S.
europepmc +1 more source
Survey and Molecular Diagnostics of Target Site Mutations Conferring Resistance to Insecticides in Populations of <i>Aphis spiraecola</i> from Greece. [PDF]
Ilias A +7 more
europepmc +1 more source
Insecticide resistance in Aedes aegypti and Aedes albopictus in southern Benin: quantification, investigation of kdr mutations, and detection of detoxification enzyme activity. [PDF]
Konkon AK +17 more
europepmc +1 more source
Click-to-Release Reactions for Tertiary Amines and Pyridines. [PDF]
Chojnacki K +9 more
europepmc +1 more source
Predicting the Stability of Base‐mediated C─H Carboxylation Adducts Using Data Science Tools
A computational approach integrating quantum chemistry and machine learning enables the prediction of CO2–adduct stability. Model interpretability and experimental validation highlight its utility for designing base‐mediated C–H carboxylation reactions.
Maike Eckhoff +6 more
wiley +2 more sources

