Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractA behavioral bioassay for analysis of rabbit nipple-search pheromone    Next Abstract"Characterization of Volatile Organic Compound Metabolites in Cigarette Smokers, Electronic Nicotine Device Users, Dual Users, and Nonusers of Tobacco" »

Acta Chem Scand (Cph)


Title:Asymmetric organic synthesis with catalytic antibodies
Author(s):Keinan E; Sinha SC; Shabat D; Itzhaky H; Reymond JL;
Address:"Scripps Research Institute, La Jolla, CA 92037, USA"
Journal Title:Acta Chem Scand (Cph)
Year:1996
Volume:50
Issue:8
Page Number:679 - 687
DOI: 10.3891/acta.chem.scand.50-0679
ISSN/ISBN:0904-213X (Print) 0904-213X (Linking)
Abstract:"The science of catalytic antibodies has undergone a rapid maturation process within its first nine years of existence. From initial 'proof of concept' and demonstration of fundamental, enzyme-like characteristics, antibodies have been shown to catalyze a remarkably broad scope of organic transformations, including difficult and unfavorable chemical reactions. Yet, the ultimate testing ground for new concepts in organic chemistry has always been the synthesis of natural products. Here we focus on several issues related to the applicability of antibody catalysis in organic synthesis. We show that (a) in the hydrophobic environment of the antibody active site, short-lived intermediates can be formed and reacted in a controlled way, thus allowing antibodies to catalyze reactions that are normally incompatible with aqueous media, (b) the intrinsic order of reactivity (chemoselectivity) in a series of structurally related enol ethers and ketals can be inverted from 1:10 in the uncatalyzed hydrolysis reaction to 1000:1 under antibody catalysis, and (c) an efficient total synthesis of alpha-multistriatin, an important, biologically active natural product can be achieved via antibody catalysis"
Keywords:"Antibodies, Catalytic/*metabolism Binding Sites Dioxolanes/*chemical synthesis Hydrogen-Ion Concentration Hydrolysis Kinetics Models, Chemical Molecular Structure Pheromones/*chemical synthesis Water;"
Notes:"MedlineKeinan, E Sinha, S C Shabat, D Itzhaky, H Reymond, J L eng GM47993/GM/NIGMS NIH HHS/ GM49736/GM/NIGMS NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. Denmark 1996/08/01 Acta Chem Scand (Cph). 1996 Aug; 50(8):679-87. doi: 10.3891/acta.chem.scand.50-0679"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 27-12-2024