Results 141 to 150 of about 7,368,504 (211)

Potentially prebiotic isocyanide activation chemistry drives RNA assembly.

Chem Commun (Camb)
Zhang SJ, Jia X, DasGupta S, Szostak JW.
europepmc   +1 more source

Phosphoric acid-catalyzed asymmetric classic Passerini reaction.

Journal of the American Chemical Society, 2015
An efficient enantioselective classic three-component Passerini reaction with a broad substrate scope in the presence of a chiral phosphoric acid catalyst has been developed. This represents the general example for classic three-component Passerini reaction with good to excellent enantioselectivies involving aromatic aldehydes and the bulky ...
Jian Zhang, Shao-Min Lin, Dao‐Juan Cheng, Xin-Yuan Liu, B. Tan   +4 more
semanticscholar   +5 more sources

Some of the next articles are maybe not open access.

Related searches:

Synthesis of d-glycopyranosyl depsipeptides using Passerini reaction.

Carbohydrate Research, 2021
A protocol based on Passerini multi-component reaction has been developed for facile, efficient and atom economical synthesis of a small library of twenty potential bioactive (2R)-2-(d-glycopyranosyl)-2-acyloxyacetamides using perbenzylated d ...
B. Kumar, Jyotirmoy Maity, B. Shankar, Sandeep Kumar, Kavita, A. Prasad   +5 more
semanticscholar   +3 more sources

On-Resin Passerini Reaction toward C-Terminal Photocaged Peptides.

Organic Letters, 2019
An on-resin, three-component Passerini reaction was developed to synthesize C-terminal photocaged peptides. Highly compatible with conventional Fmoc SPPS, this reaction produces peptides with a C-terminal o-amido-6-nitroveratryl (αANV) ester in one pot ...
Wing-Ho So, Jiang Xia
semanticscholar   +3 more sources

Passerini Reaction

Name Reactions, 2021
J. Li
semanticscholar   +2 more sources

Microdroplet Chemistry Accelerating a Three-Component Passerini Reaction for α-Acyloxy Carboxamide Synthesis.

Journal of Organic Chemistry, 2023
α-Acyloxy carboxamides are important multifunctional natural products that show bioactive and pharmacological activities. Traditional three-component Passerini reactions among isocyanates, aldehydes/ketones, and carboxylic acids for affording α-acyloxy ...
Yi-Kang Wu, Heyong Cheng, Jiayao Li, Jin-Hua Liu, Jian-Nan Sun   +4 more
semanticscholar   +1 more source

New oxacycles on the block: benzodioxepinones via a Passerini reaction

Molecular Diversity, 2022
Oxacycles and benzoxepanes are privileged motifs present in a variety of natural products and functional molecules. However, their synthetic access is limited. Here, we demonstrate a rapid synthesis of unprecedented benzoxepanes from readily available starting materials in one step via a Passerini multicomponent reaction. The reaction proceeds smoothly
Michael Fragkiadakis, Marios Zingiridis, Edward Loukopoulos, C. Neochoritis   +3 more
semanticscholar   +3 more sources

Drug Discovery for Soft Drugs on TRPV1 and TRPM8 Channels Using the Passerini Reaction.

Methods in molecular biology, 2019
Multicomponent transformations, such as Ugi and Passerini reactions, allow for the fast synthesis of libraries of medium complexity, avoiding the formation of waste residues and significantly reducing time and money expenditure. Although the Ugi reaction
T. Pirali, Ubaldina Galli, Marta Serafini, Alessia Griglio, A. Genazzani, G. Tron   +5 more
semanticscholar   +2 more sources

Enediyne-Comprising Amino Aldehydes in the Passerini Reaction

ACS Combinatorial Science, 2018
Multicomponent reactions represent a highly efficient approach to a broad spectrum of structurally diverse compounds starting from simple and affordable compounds. A focused library of tweezers-like compounds is prepared by employing the multicomponent Passerini reaction comprising enediyne-derived amino aldehydes.
Ivanka Jeric, Matija Gredičak
exaly   +3 more sources

The Passerini Reaction

ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
BANFI, LUCA, RIVA, RENATA
openaire   +2 more sources