Irreversible inhibitors of serine, cysteine, and threonine proteases

JC Powers, JL Asgian, ÖD Ekici, KE James - Chemical reviews, 2002 - ACS Publications
Proteases or proteolytic enzymes form one of the largest and more important groups of
enzymes. Proteases selectively catalyze the hydrolysis of peptide bonds and can be divided …

Asymmetric synthesis of β‐lactams by staudinger ketene‐imine cycloaddition reaction

C Palomo, JM Aizpurua, I Ganboa… - European journal of …, 1999 - Wiley Online Library
Cycloaddition reactions between ketenes, bearing amino‐, oxy‐, or halo‐groups, and imines
are recognized as being amongst the most important and direct routes to β‐lactams. Alkyl …

[图书][B] Organofluorine chemistry

K Uneyama - 2008 - books.google.com
The replacement of hydrogen with fluorine in organic molecules can profoundly influence
their chemical and physical properties, leading to a range of compounds with highly …

Profiling serine hydrolase activities in complex proteomes

D Kidd, Y Liu, BF Cravatt - Biochemistry, 2001 - ACS Publications
Serine hydrolases represent one of the largest and most diverse families of enzymes in
higher eukaryotes, comprising numerous proteases, lipases, esterases, and amidases. The …

Exceptionally potent inhibitors of fatty acid amide hydrolase: the enzyme responsible for degradation of endogenous oleamide and anandamide

DL Boger, H Sato, AE Lerner… - Proceedings of the …, 2000 - National Acad Sciences
The development of exceptionally potent inhibitors of fatty acid amide hydrolase (FAAH), the
enzyme responsible for the degradation of oleamide (an endogenous sleep-inducing lipid) …

Enantioselective decarboxylative alkylation reactions: catalyst development, substrate scope, and mechanistic studies

DC Behenna, JT Mohr, NH Sherden… - … A European Journal, 2011 - Wiley Online Library
Abstract α‐Quaternary ketones are accessed through novel enantioselective alkylations of
allyl and propargyl electrophiles by unstabilized prochiral enolate nucleophiles in the …

The recent impact of solid-phase synthesis on medicinally relevant benzoannelated nitrogen heterocycles

S Bräse, C Gil, K Knepper - Bioorganic & medicinal chemistry, 2002 - Elsevier
Benzoannelated heterocycles such as benzodiazepines and indoles can be prepared
efficiently through cyclization on solid supports, although no single approach is currently …

Polyfluorinated ethanes as versatile fluorinated C2-building blocks for organic synthesis

VG Nenajdenko, VM Muzalevskiy, AV Shastin - Chemical reviews, 2015 - ACS Publications
Fluorinated compounds attracted remarkable interest in recent decades. 1 Unique complex
of physicochemical and biological properties provided by incorporation of fluorine or …

Viral proteases

L Tong - Chemical Reviews, 2002 - ACS Publications
Viruses are major pathogenic agents that can cause a variety of serious diseases in
humans, other animals, and plants. Due to their clinical and scientific importance, viruses …

β-Lactams as versatile synthetic intermediates for the preparation of heterocycles of biological interest

B Alcaide, P Almendros - Current medicinal chemistry, 2004 - ingentaconnect.com
Since the advent of penicillin, the β-lactam antibiotics have been the subject of much
discussion and investigation, within both the scientific and public sectors. The primary …