Skip to Content
Merck
CN
Search Within
Applications
Content Type

CH functionalization

Applied Filters:
facet applications:CH functionalization
facet content type:Technical Article
Palau’Chlor®: Easily and Selectively Functionalize Lead Compounds
Aryl chlorides are commonly used in cross-coupling reactions and can serve as key intermediates towards the synthesis of pharmaceutical drug candidates and natural products.
Recent Advances in the Catalytic Transformations
This article details the latest progress in synthesizing alkylsulfonyl fluorides through different approaches that utilize photoredox catalysis, electrocatalysis, transition-metal catalysis, and organocatalysis. The alkylsulfonyl fluorides thus prepared could be utilized further in sulfur(VI) fluoride exchange (SuFEx) click reactions.
SuFEx: Sulfonyl Fluorides that Participate in the Next Click Reaction
In collaboration with K. Barry Sharpless and coworkers, we offer a variety of sulfonyl fluoride reagents that undergo a “Click II” reaction.
Baran Diversinates™
Rapidly diversify (hetero)aromatic scaffolds for chemical industry needs amid resource and time constraints, ensuring efficiency.
White Catalyst
The "White catalyst" by Professor M. Christina White enables allylic carbon functionalization, demonstrating exceptional catalytic activity.
Baran Diversinates™
Rapidly diversify (hetero)aromatic scaffolds for chemical industry needs amid resource and time constraints, ensuring efficiency.
MCAT- 53™ Catalyst for Ruthenium Formation
A recyclable, ligand-free ruthenium catalyst for C–H activation reactions and concomitant C–C bond formation in the presence of water.
Electrochemical Allylic C–H Oxidation
Phil Baran develops ALD00564 reagent as a safe, cost-effective alternative for allylic oxidations and cross-coupling reactions.
Ellman's Sulfinamides
Ellman's sulfinamide is available in both enantiomeric and racemic forms for your research. This versatile and useful auxiliary has found extensive use both in academics and industry.
C–H Amination
Stanford's Du Bois group advances Rh-catalyzed C–H amination, producing heteroatom motifs in ring heterocycles.
Jørgensen’s Organocatalysts
Professor Karl Anker Jørgensen and his group have developed ethers which serve as excellent chiral organocatalysts in the direct asymmetric α-functionalization of aldehydes.
Rh2(esp)2 Catalyst
New! Rh2(esp)2, and exceptionally efficient and selective catalyst for C-H amination.
Role of High Purity Metal Salts in Chemical Synthesis
Discover the ways in which high-purity metal salts improve the selectivity, yields, and catalytic efficacy of organic synthesis reactions.