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Side reactions in peptide synthesis / (Record no. 247157)

000 -LEADER
fixed length control field 05537cam a2200589Ki 4500
001 - CONTROL NUMBER
control field ocn920551933
003 - CONTROL NUMBER IDENTIFIER
control field OCoLC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20190328114812.0
006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS
fixed length control field m o d
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
fixed length control field cr cnu---unuuu
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 150909t20152016enk o 001 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency OPELS
Language of cataloging eng
Description conventions rda
-- pn
Transcribing agency OPELS
Modifying agency YDXCP
-- OCLCF
-- N$T
-- IDEBK
-- EBLCP
-- OCLCQ
-- ESU
-- DEBBG
-- B3G
-- BRA
-- MERUC
-- COS
-- COF
-- U3W
-- D6H
-- ESEHU
-- AU@
-- OCLCQ
-- WYU
-- OCLCA
-- MERER
-- OCLCO
-- OCLCA
-- OCLCQ
066 ## - CHARACTER SETS PRESENT
Alternate G0 or G1 character set (S
019 ## -
-- 1066447827
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9780128011812
Qualifying information (electronic bk.)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 0128011815
Qualifying information (electronic bk.)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Canceled/invalid ISBN 9780128010099
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Canceled/invalid ISBN 0128010096
035 ## - SYSTEM CONTROL NUMBER
System control number (OCoLC)920551933
Canceled/invalid control number (OCoLC)1066447827
050 #4 - LIBRARY OF CONGRESS CALL NUMBER
Classification number QP552.P4
060 00 - NATIONAL LIBRARY OF MEDICINE CALL NUMBER
Classification number 2016 A-909
060 10 - NATIONAL LIBRARY OF MEDICINE CALL NUMBER
Classification number QU 68
072 #7 - SUBJECT CATEGORY CODE
Subject category code SCI
Subject category code subdivision 007000
Source bisacsh
082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 572/.65
Edition number 23
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Yang, Yi,
Relator term author.
245 10 - TITLE STATEMENT
Title Side reactions in peptide synthesis /
Medium [electronic resource]
Statement of responsibility, etc. Yi Yang.
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture London, UK :
Name of producer, publisher, distributor, manufacturer Academic Press is an imprint of Elsevier,
Date of production, publication, distribution, manufacture, or copyright notice 2015.
264 #4 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice �2016
300 ## - PHYSICAL DESCRIPTION
Extent 1 online resource
336 ## - CONTENT TYPE
Content type term text
Content type code txt
Source rdacontent
337 ## - MEDIA TYPE
Media type term computer
Media type code c
Source rdamedia
338 ## - CARRIER TYPE
Carrier type term online resource
Carrier type code cr
Source rdacarrier
520 ## - SUMMARY, ETC.
Summary, etc. This valuable handbook is ideal for research and process chemists working with peptide synthesis in diverse settings across academic, biotech, and pharmaceutical research and development. While peptide chemistry is increasingly prevalent, common side reactions and their causes are often poorly understood or anticipated, causing unnecessary waste of materials and delay. Each chapter discusses common side reactions through detailed chemical equations, proposed mechanisms (if any), theoretical background, and finally, a variety of possible solutions to avoid or alleviate the specified side reaction.
500 ## - GENERAL NOTE
General note Includes index.
588 0# - SOURCE OF DESCRIPTION NOTE
Source of description note Title details screen (ScienceDirect, viewed September 9, 2015).
505 0# - FORMATTED CONTENTS NOTE
Linkage 880-01
Formatted contents note Cover; Title Page; Copyright Page; Dedication; Contents; Preface; Chapter 1 -- Peptide Fragmentation/Deletion Side Reactions; 1.1 -- Acidolysis of peptides containing N-Ac-N-alkyl-Xaa motif; 1.2 -- des-Ser/Thr impurities induced by O-acyl isodipeptide Boc-Ser/Thr(Fmoc-Xaa)-OH as building block for peptide synthesis; 1.3 -- Acidolysis of -N-acyl-N-alkyl-Aib-Xaa- bond; 1.4 -- Acidolysis of -Asp-Pro- bond; 1.5 -- Autodegradation of peptide N-terminal H-His-Pro-Xaa- moiety; 1.6 -- Acidolysis of the peptide C-terminal N-Me-Xaa; 1.7 -- Acidolysis of peptides with N-terminal FITC modification.
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note 3.3 -- Formation of Trp-EDT and Trp-EDT-TFA adduct in peptide global deprotection3.4 -- Trp dimerization side reaction during peptide global deprotection; 3.5 -- Trp reduction during peptide global deprotection; 3.6 -- Cys alkylation during peptide global deprotection; 3.7 -- Formation of Cys-EDT adducts in peptide global deprotection reaction; 3.8 -- Peptide sulfonation in side chain global deprotection reaction; 3.9 -- Premature Acm cleavage off Cys(Acm) and Acm Sb2s!O migration during peptide global deprotection.
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note 3.10 -- Methionine alkylation during peptide side chain global deprotection with DODT as scavenger3.11 -- Thioanisole-induced side reactions in peptide side chain global deprotection; References; Chapter 4 -- Peptide Rearrangement Side Reactions; 4.1 -- Acid catalyzed acyl Nb2s! migration and the subsequent peptide acidolysis; 4.2 -- Base catalyzed acyl Ob2s! migration; 4.3 -- His-Nim- induced acyl migration; References; Chapter 5 -- Side Reactions Upon Amino Acid/Peptide Carboxyl Activation; 5.1 -- Formation of N-acylurea upon peptide/amino acid-carboxyl activation by DIC.
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note 5.8 -- Peptide chain termination through the formation of peptide N-terminal urea in CDI-mediated coupling reaction.
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc Includes bibliographical references and index.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Peptides
General subdivision Synthesis.
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Peptides
General subdivision Synthesis.
Source of heading or term fast
Authority record control number (OCoLC)fst01057580
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element SCIENCE
General subdivision Life Sciences
-- Biochemistry.
Source of heading or term bisacsh
650 12 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Peptide Biosynthesis.
Authority record control number (DNLM)D010452
650 22 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Peptides
General subdivision chemistry.
Authority record control number (DNLM)D010455Q000737
650 22 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Drug-Related Side Effects and Adverse Reactions.
Authority record control number (DNLM)D064420
655 #4 - INDEX TERM--GENRE/FORM
Genre/form data or focus term Electronic books.
655 #0 - INDEX TERM--GENRE/FORM
Genre/form data or focus term Electronic book.
856 40 - ELECTRONIC LOCATION AND ACCESS
Materials specified ScienceDirect
Uniform Resource Identifier http://www.sciencedirect.com/science/book/9780128010099
880 8# - ALTERNATE GRAPHIC REPRESENTATION
Linkage 505-00/(S
a 1.8 -- Acidolysis of thioamide peptide1.9 -- Deguanidination side reaction on Arg; 1.10 -- DKP (2,5-diketopiperazine) formation; References; Chapter 2 -- (Sb(B-Elimination Side Reactions; 2.1 -- (Sb(B-Elimination of Cys sulfhydryl side chain; 2.2 -- (Sb(B-Elimination of phosphorylated Ser/Thr; References; Chapter 3 -- Peptide Global Deprotection/Scavenger-Induced Side Reactions; 3.1 -- Tert-butylation side reaction on Trp during peptide global deprotection; 3.2 -- Trp alkylation by resin linker cations during peptide cleavage/global deprotection.
880 8# - ALTERNATE GRAPHIC REPRESENTATION
Linkage 505-01/(S
a 5.2 -- Uronium/Guanidinium salt coupling reagents-induced amino group guanidination side reactions5.3 -- (Se(B-lactam formation upon Arg activation reaction; 5.4 -- NCA formation upon Boc/Z-Amino acid activation; 5.5 -- Dehydration of side chain-unprotected Asn/Gln during carboxyl-activation; 5.6 -- Formation of H-(Sb(B-Ala-OSu from HOSu-carbodiimide reaction during amino acid carboxyl-activation; 5.7 -- Benzotriazinone ring opening and peptide chain termination during carbodiimide/HOOBt mediated coupling reactions.

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Last Updated on September 15, 2019
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