Mitsunobu and related reactions: advances and applications

KCK Swamy, NNB Kumar, E Balaraman… - Chemical …, 2009 - ACS Publications
The substitution of primary or secondary alcohols with nucleophiles mediated by a redox
combination of a trialkylor triarylphosphine and a dialkyl azodicarboxylate is popularly …

[HTML][HTML] Synthesis of ruthenium complexes and their catalytic applications: A review

J Hafeez, M Bilal, N Rasool, U Hafeez… - Arabian Journal of …, 2022 - Elsevier
Ruthenium complexes are an important class that has multiple catalytic and biological
applications. Ruthenium has a remarkably broad and diversified chemical spectrum. In the …

The Mitsunobu reaction: origin, mechanism, improvements, and applications

TYS But, PH Toy - Chemistry–An Asian Journal, 2007 - Wiley Online Library
The Mitsunobu reaction is a widely used and versatile method for the dehydrative oxidation–
reduction condensation of an acid/pronucleophile usually with a primary or secondary …

Potent and Selective Oxidatively Labile Ether‐Based Prodrugs through Late‐Stage Boronate Incorporation

PJ Geaneotes, CP Janosko, C Afeke… - Angewandte …, 2024 - Wiley Online Library
This manuscript describes a new strategy for prodrug synthesis in which a relatively inert
ether group is introduced at an early stage in a synthetic sequence and functionalized in the …

Vanadium-catalyzed asymmetric oxidation of α-hydroxy esters using molecular oxygen as stoichiometric oxidant

AT Radosevich, C Musich, FD Toste - Journal of the American …, 2005 - ACS Publications
A vanadium-catalyzed method for the oxidative kinetic resolution of α-hydroxyesters, using
oxygen as the terminal oxidant, is described. The catalyst is generated in situ from vanadium …

Design of PSMA ligands with modifications at the inhibitor part: an approach to reduce the salivary gland uptake of radiolabeled PSMA inhibitors?

VB Felber, MA Valentin, HJ Wester - EJNMMI Radiopharmacy and …, 2021 - Springer
Aim To investigate whether modifications of prostate-specific membrane antigen (PSMA)-
targeted radiolabeled urea-based inhibitors could reduce salivary gland uptake and thus …

Synthesis of all nineteen appropriately protected chiral α-hydroxy acid equivalents of the α-amino acids for Boc solid-phase depsi-peptide synthesis

S Deechongkit, SL You, JW Kelly - Organic letters, 2004 - ACS Publications
The preparation of depsi-peptides, amide-to-ester-substituted peptides used to probe the
role of hydrogen bonding in protein folding energetics, is accomplished by replacing specific …

Efficient Synthesis of β2-Amino Acid by Homologation of α-Amino Acids Involving the Reformatsky Reaction and Mannich-Type Imminium Electrophile

R Moumne, S Lavielle, P Karoyan - The Journal of Organic …, 2006 - ACS Publications
Development of new methods for the synthesis of β-amino acids is important as polymers of
these compounds are promising peptidomimetic candidates in medicinal chemistry. We …

Identification of Furan Metabolites Derived from Cysteine−cis-2-Butene-1,4-dial−Lysine Cross-Links

D Lu, LA Peterson - Chemical research in toxicology, 2010 - ACS Publications
Furan is a rodent hepatotoxicant and carcinogen. Because this compound is an important
industrial intermediate and has been detected in heat-processed foods and smoke, humans …

Metal-Free Cross-Dehydrogenative C–O Coupling of Carbonyl Compounds with N-Hydroxyimides: Unexpected Selective Behavior of Highly Reactive Free Radicals …

IB Krylov, ER Lopat'eva, AS Budnikov… - The Journal of …, 2019 - ACS Publications
Cross-dehydrogenative C–O coupling of N-hydroxyimides with ketones, esters, and
carboxylic acids was achieved employing the di-tert-butyl peroxide as a source of free …