Reagents for Glycoside, Nucleotide, and Peptide Synthesis
(Sprache: Englisch)
The Synthesis of biopolymers and their conjugates is of ever increasing importance in bioorganic chemistry and chemical biology. As the need for such systems becomes ever more widespread, their synthesis is necessarily practiced in a broader spectrum of...
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The Synthesis of biopolymers and their conjugates is of ever increasing importance in bioorganic chemistry and chemical biology. As the need for such systems becomes ever more widespread, their synthesis is necessarily practiced in a broader spectrum of laboratories beyond the specialized ones that have traditionally concentrated in the area.
Klappentext zu „Reagents for Glycoside, Nucleotide, and Peptide Synthesis “
The Synthesis of biopolymers and their conjugates is of ever increasing importance in bioorganic chemistry and chemical biology. As the need for such systems becomes ever more widespread, their synthesis is necessarily practiced in a broader spectrum of laboratories beyond the specialized ones that have traditionally concentrated in the area. For each type of biopolymer there exists a wide array of protecting systems and coupling reagents from which the practitioner must make and informed choice. This Handbook presents short, informative articles on approximately 250 of the most widely used reagents in the area in a single, affordable volume so as to facilitate the task of the experimentalist. Each of the articles, drawn from the e-EROS database, is written by an experienced worker in the area and collects together a summary of the most pertinent reactions for every reagent with references to the original literature. Each article also contains an overview of the physical properties of the reagent, conditions for its storage, and purification methods. This Handbook will prove of highest value to virtually everybody working in organic synthesis, medicinal chemistry or natural product chemistry.All the information compiled in this volume is also available in electronic format on Wiley InterScience. The electronic Encyclopedia of Reagents for Organic Synthesis (e-EROS) includes all the reagents described in this volume plus many more reagents of other types and for other uses. e-EROS allows for both text and structure searches and has many new and updated entries added every year.
For more information visit:
http://www.mrw.interscience.wiley.com/eros/
Inhaltsverzeichnis zu „Reagents for Glycoside, Nucleotide, and Peptide Synthesis “
Preface. Introduction. Recent review Artilces and Monogrpahs. Acetonitrile. p Acetoxybenzyl Bromide. 2 [(1 Acetyl 2 oxopropyl)thio] 1H isoindole 1,3(2H) dione. 2 Adamantyl Chloroformate. N [(Allyloxycarbonyl)oxy]maleimide styrene Copolymer (Alloc resin). Allyl Tetraisopropylphosphoramidite. Allyl Trichloroacetimidate. Anthracenesulfonamide. O (7 Azabenzotriazol 1 yl) 1,3 dimethyl 1,3 dimethyleneuronium Hexafluorophosphate. (7 Azabenzotriazol 1 yloxy)tris(pyrrolidino)phosphonium Hexafluorophosphate. Axidotris(dimethylamino Phosphonium Hexafluorophosphate. 7 Azabenzotriazol 1 yloxytris(dimethylamino)Phosphonium Hexafluorophosphate. Azidotris(dimethylamino)Phosphonium. Hexafluorophosphate. Benzeneselenenyl Bromide. Benzeneselenenyl Trifluoromethanesulfonate. Benzenesulfenyl Chloride. Benzenesulfenyl Trifluoromethanesulfonate. 1 Benzenesulfinyl Piperidine. Benzimidazolium Trifluoromethanesulfonate. 3H 1,2 Benzodithiol 3 one 1, 1 Dioxide. 1, 3 Benzodithiol 1 ium Tetrafluoroborate. Benzothianthrene Oxide. 3H 1,2 Benzothiaselenol 3 one. Benzothiazole 2 sulfonyl chloride (BtsC1). 1 Benzotriazolyl Diethyl Phosphate (BDP). Benzotriazol 1 yloxytris(dimethylamino)phosphonium. Hexafluorophosphate (BOP). (1H Benzotriazol 1 yloxy)tris(pyrrolidino)phosphonium. Hexafluorophosphate. O Benzotriazol 1 yl N,N,N ,N tetramethyluronium. Hexafluorophosphate. O Benzotriazol 1 yl N,N,N ,N tetramethyluronium. Tetrafluoroborate. Benzyl Bromide. Benzyl Chloroformate. Benzyl 2 Hydroxymethylbenzoate. Benzyl Isopropenyl Ether. Benzyl 2,2,2, Trichloroacetimidate. N,N Bis(t butoxycarbony1) N Trifluoromethanesulfonyl Guanidine. 1,3 Bis(2,2 dimethyl 1,3 dioxolan 4 ylmethyl)carbodiimide(BDDC). Bis(2,4 dinitrophenyl)Carbonate. Bis(1 methoxy 2 methyl 1 propenyloxy)dimethylsilane. N Bis(methylthio)methylene p toluenesulfonamide. Bis(4 nitrophenyl)Carbamate. Bis(p nitrophenyl) Hydrogen Phosphate. Bis(o nitrophenyl)Phenylphosphonate. Bis(p nitrophenyl)Phenylphosphonate. Bis(2 oxo 3 oxazolidinyl)Phosphinic
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Chloride. Bis(pentafluorophenyl)Caronate. Bis(o phenylene)Pyrophosphite. 1,2 Bis(phenylsulfonyl)ethylene. 1,1,3,3 Bis9tetramethylene)chlorouronium. Hexafluorophosphate. Bis(tributyltin)Oxide.Bis(2,2,2 trichloroethyl)Azodicarboxylate. Bis(2,2,2 trichloroethyl)Phosphorochloridate. Bis(trichloromethyl)carbonate. 2,7 Bis(trimethylsily)Fluorenylmethyl Chloroformate. p Bromobenzyl Bromide. 3 Bromocyclohexene. 2 Bromo 1 ethylpyridinium Tetrafluoroborate (BEP). Bromonium Di sym collidine Perchlorate. N Bromosuccinimide. Bromotripyrrolidinophosphonium Hexafluorophosphate. 1 N (t Butoxycarbonyl) 1H benzotriazole 3N oxide. 1 (t Butoxycarbonyl)imidazole. 2 (t Butoxycarbonyloxyimino) 2 phenylacetonitrile. t Butyl Chloroformate. Cadmium Carbonate. Carbomethoxysulfenyl Chloride. 1,1 Caronylbis(3 methylimidazolium). Bis(trifluoromethanesulfonate). N,N Carbonyldiimidazole. Chloroacety Chloride. 2 Chloro 4H 1,3,2 benzodioxaphosphorin 4 one. p Chlorobenzyl Bromide. 6 Chloro 2,4 dimethoxy s triazine. 2 Chloro 1,3 dimethylimidazolidium Hexafluorophosphate. 2 chloro 1 methylpyridinium Iodide. 2 Chloro 4,4,5,5 ttramethyl 1,3,2 dioxaphospholane. 1 Chloro N,N,2 trimethylpropenylamine. ChlorotripyrrolidmopnospnoniumHexafluorophosphate. 2,4,6 Collidine. 2 Cyanoethyl Diisopropylchlorophosphoramidite. 2 cyanoethylphosphoric Acid. 2 Cyanoethyl Tetraisopropylphosphorodiamidite. Cyanuric Fluoride. Cyclohexyl Chloroformate. 1 Cyclohexyl 3 (2 morpholineothyl)carbodiimide. 1 Cyclohexyl 3 (2 morpholinoethyl)Carbodiimide. Metho p toluenesulfonate. 17H Cyclopental[1,2 1,:2,4 1 ]diphenanthren 17 yl Chloroformate. a Cyclopropylcyclopropanemethanol. Dibenzyl N,N Diisopropylphosphoramidite. Dibenzylphosphite. 2,7, Dibromo 9H Fluoren 9 Ylmethyl Chloroformate. Dibromomethylbenzene. Dibromomethyl Methyl Ether. Di t butyl Dicarbonate. 2,7 Di t Butyl 9 fluorenylmethyl Chloroformate. 2,6 Di t butylmethylpryridine. Di n butyltin Oxide. Dichlorobis(cyclopentadienyl)hafnium Silver(I) Salts. Dichloromethyl Methyl Ethe
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Autoren-Porträt von David Crich
David Crich was born in 1959; BSc, Surrey University, 1981; DEsSc, University of Paris, 1984; Postdoctoral Fellow, Institut de Chimie des Substances Naturelles, 1984-1985; Lecturer, University College, London, 1985-1990; Laureat of the Academy of Sciences (France) 1989; Corday Morgan Medal (Royal Society of Chemistry), 1990; University of Illinois Scholar, 1992; Visiting Professor, University of Aix-Marseille, 1992: Fellow of the A. P. Sloan Foundation, 1994-1996; Tate and Lyle Carbohydrate Chemistry Medal (Royal Society of Chemistry), 1995. Since1997 Distinguished Professor of Organic Chemistry at the University of Illinois at Chicago. Since 2001 on the Editorial Board of e-EROS.
Bibliographische Angaben
- Autor: David Crich
- 2005, 1. Auflage, 450 Seiten, Maße: 27,9 cm, Gebunden, Englisch
- Verlag: Wiley & Sons
- ISBN-10: 047002304X
- ISBN-13: 9780470023044
Sprache:
Englisch
Pressezitat
" a very valuable, encyclopedic addition to virtually any organic / synthetic / medicinal chemistry laboratory." (Journal of Medicinal Chemistry, 2006, Vol. 49, No. 7) "A high caliber reference work" ( organic chemistry.org, August 06)
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