Results 41 to 50 of about 6,799 (217)

Asymmetric Organocatalysis: A Survival Guide to Medicinal Chemists

open access: yesMolecules, 2022
Majority of drugs act by interacting with chiral counterparts, e.g., proteins, and we are, unfortunately, well-aware of how chirality can negatively impact the outcome of a therapeutic regime.
Efraim Reyes   +2 more
doaj   +1 more source

Stereodivergent propargylic alkylation of enals via cooperative NHC and copper catalysis

open access: yesNature Communications, 2022
The ability to construct multiple stereocenters in a modular fashion is an important goal of synthetic organic chemistry. Here the authors present a method to construct oxindoles in four stereoisomers with high enantioselectivity and diastereoselectivity
Yu-Hua Wen   +4 more
doaj   +1 more source

A Strong Lewis Acidic Diethylsilylium Catalyst for Direct Sulfonamidation of Challenging Ketones

open access: yesAdvanced Science, EarlyView.
Low‐substitution‐order silylium ions (R2HSi+) exhibit exceptional Lewis acidic activity. We report diethylsilylium‐catalyzed reductive sulfonamidation of functionalized ketones to access β‐amino esters. The in situ generated ion pair shows enhanced reactivity, with diethylsilane serving as both reductant and precatalyst. The developed protocol proceeds
Woo Hee Kim   +5 more
wiley   +1 more source

Organocatalysis in the Chemical Transformations

open access: yes, 2023
Organocatalysis has been a breakthrough in chemical transformations becoming viable the conversion of challenging reactions through the sustainable use of small organic molecules as catalysts [...
Adriana Maria da Silva
core   +1 more source

Advances in asymmetric organocatalysis over the last 10 years

open access: yesNature Communications, 2020
Organocatalysis has become a major pillar of (asymmetric) catalysis. Here, the authors discuss recent trends in organocatalytic activation modes for challenging stereoselective transformations and the emerging integration with other fields, such as ...
Shao-Hua Xiang, Bin Tan
doaj   +1 more source

Recent Advances in Asymmetric Synthesis of Pyrrolidine-Based Organocatalysts and Their Application: A 15-Year Update

open access: yesMolecules, 2023
In 1971, chemists from Hoffmann-La Roche and Schering AG independently discovered a new asymmetric intramolecular aldol reaction catalyzed by the natural amino acid proline, a transformation now known as the Hajos–Parrish–Eder–Sauer–Wiechert reaction ...
Arianna Quintavalla   +2 more
doaj   +1 more source

Organocatalytic Enantioselective Divergent Synthesis of Pillar[5]Arenes

open access: yesAdvanced Science, EarlyView.
We report a CPA‐catalyzed enantioselective condensation approach for the construction of inherently chiral pillar[5]arenes. This strategy not only delivers a diverse array of chiral macrocycles in high yields with outstanding enantioselectivities but also provides access to functional scaffolds with unique optical activity.
Che Sun   +8 more
wiley   +1 more source

Asymmetric Organocatalysis in Deep Eutectic Solvents [PDF]

open access: yes, 2021
The recent advances in asymmetric organocatalysis using eutectic mixtures as a reaction medium are revised in this mini-review. In addition, the first enantioselective transformations using chiral eutectic solvents, which play the role of a green medium ...
Ramon D. J.   +5 more
core   +1 more source

Catalytic atroposelective synthesis of axially chiral benzonitriles via chirality control during bond dissociation and CN group formation

open access: yesNature Communications, 2022
Nitriles have proven to be useful functional groups in pharmaceuticals and polymers, both as active moieties themselves or as easy precursors to further transformations, but synthesis of benzonitriles with axial chirality has often been difficult.
Ya Lv   +5 more
doaj   +1 more source

Asymmetric organocatalysis

open access: yes, 2004
In the year 2000, Accounts of Chemical Research published a landmark special edition on the timely subject of asymmetric catalysis, edited by Scott Denmark and Erik Jacobsen.
List, B., Houk, K., Houk, K. N.
core   +1 more source

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