MARC

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010 |a  2004271923 
035 |a (OCoLC)ocm55502600  
040 |a DLC  |b eng  |e rda  |c DLC  |d EQO  |d OHX  |d UAT  |d BAKER  |d NLGGC  |d BTCTA  |d LVB  |d YDXCP  |d HEBIS  |d DEBBG  |d OCLCF  |d OCLCO  |d OCLCQ  |d IPL  |d OCLCQ  |d OCLCO  |d PAU  |d BGU  |d OCLCO  |d UKMGB  |d OCLCQ  |d OCLCO  |d OCLCL 
016 7 |a 968760139  |2 DE-101 
016 7 |a 012934067  |2 Uk 
019 |a 54054197 
020 |a 1588902358  |q (TNY, New York) 
020 |a 9781588902351  |q (TNY, New York) 
020 |a 3131370033  |q (GTV, Stuttgart) 
020 |a 9783131370037  |q (GTV, Stuttgart) 
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029 1 |a DEBBG  |b BV019377804 
029 1 |a HEBIS  |b 11791794X 
029 1 |a NLGGC  |b 259371602 
029 1 |a NZ1  |b 8496811 
029 1 |a UKMGB  |b 012934067 
029 1 |a YDXCP  |b 100450814 
035 |a (OCoLC)55502600  |z (OCoLC)54054197 
050 0 0 |a QD262  |b .K59 2004 
072 7 |a QD  |2 lcco 
082 0 4 |a 547/.2  |2 21 
084 |a 35.52  |2 bcl 
084 |a VK 5500  |2 rvk 
049 |a MAIN 
100 1 |a Kocienski, Philip J,  |e author 
245 1 0 |a Protecting groups /  |c Philip J. Kocieński. 
250 |a 3rd ed. 
264 1 |a Stuttgart ;  |a New York :  |b Georg Thieme,  |c [2004] 
264 4 |c ©2004 
300 |a xvi, 679 pages :  |b illustrations (some color) ;  |c 25 cm 
336 |a text  |b txt  |2 rdacontent 
337 |a unmediated  |b n  |2 rdamedia 
338 |a volume  |b nc  |2 rdacarrier 
504 |a Includes bibliographical references and index. 
505 0 0 |t Death, Taxes, and Protecting Groups --  |t Deprotection: The Concept of Orthogonal Sets --  |t Protecting Groups Cleaved by Basic Solvolysis --  |t Protecting Groups Cleaved by Acid --  |t Protecting Groups Cleaved by Heavy Metals --  |t Protecting Groups Cleaved by Fluoride Ions --  |t Protecting Groups Cleaved by Reductive Elimination --  |t Protecting Groups Cleaved by [beta]-Elimination Reactions --  |t Protecting Groups Cleaved by Hydrogenolysis --  |t Protecting Groups Cleaved by Oxidation --  |t Protecting Groups Cleaved by Dissolving Metal Reduction --  |t Protecting Groups Cleaved by Nucleophilic Substitution --  |t Protecting Groups Cleaved by Transition Metal Catalysis --  |t Protecting Groups Cleaved by Light --  |t Protecting Groups Cleaved by Enzymes --  |t Relay Deprotection --  |t Transprotection --  |t Mutual Protection --  |t Temporary Protection --  |t Protecting Groups As Not-So-Innocent Bystanders --  |t Neighbouring Group Participation --  |t Conformational and Electronic Effects --  |t Co-ordination Effects --  |t Protecting Groups and Solid-Phase Synthesis --  |t General Reviews on Protecting Groups --  |t Reviews on Enzyme-Labile Protecting Groups --  |t Reviews on Photo-Labile Protecting Groups --  |t Reviews on Linkers in Solid-Phase Synthesis --  |t Reviews on the Synthesis of Complex Targets Including Discussion of Protecting Group Problems and Strategies --  |t Carbonyl Protecting Groups --  |t O, O-Acetals --  |t Cyclic Acetals --  |t O, O-Acetals in Asymmetric Synthesis --  |t Acyclic O, O-Acetals --  |t S, S-Acetals --  |t O, S-Acetals --  |t N, O-Acetals --  |t Cyanohydrins --  |t Orthoester Derivatives --  |t O, O, O-Orthoesters --  |t O, S, S-Orthoesters. 
505 8 0 |t S, S, S-Orthoesters --  |t Oxazolines --  |t Reviews Concerning the Preparation of O, O-Acetals and Their Use as Protecting Groups --  |t Reviews Concerning the Mechanism for Hydrolysis of Acetals --  |t Reviews Concerning O, O-Acetals as Reactive Functionality --  |t Reviews Concerning the Preparation, Chemistry, and Hydrolysis of O, S- and S, S-Acetals --  |t Reviews Concerning the Synthesis and Reactions of N, O-Acetals and Their Use in Asymmetric Synthesis --  |t Reviews Concerning the Chemistry of Orthoesters and Oxazolines --  |t Diol Protecting Groups --  |t O, O-Acetals --  |t Isopropylidene Acetals --  |t Cyclopentylidene and Cyclohexylidene Acetals --  |t The Arylmethylene Acetal Family --  |t Methylene Acetals --  |t Diphenylmethylene Acetals --  |t 1,2-Diacetals --  |t Dispoke Derivatives --  |t Cyclohexane-1,2-diacetals --  |t Butane-2,3-diacetals --  |t Silylene Derivatives --  |t 1,1,3,3-Tetraisopropyldisiloxanylidene Derivatives --  |t N, O-Acetals for the Protection of 1,2- and 1,3-Amino Alcohols --  |t Reviews Concerning the Protection of 1,2- and 1,3-Diols --  |t Reviews Concerning Acetal Derivatives of Carbohydrates --  |t Reviews Concerning 1,2-Diacetals --  |t Reviews Concerning N, O-Acetals --  |t Hydroxyl Protecting Groups --  |t Silyl Ethers --  |t Trimethylsilyl (TMS) Ethers --  |t Triethylsilyl (TES) Ethers --  |t tert-Butyldimethylsilyl (TBS) Ethers --  |t tert-Butyldiphenylsilyl (TBDPS) Ethers --  |t Triisopropylsilyl (TIPS) Ethers --  |t Diethylisopropylsilyl (DEIPS) Ethers --  |t Thexyldimethylsilyl (TDS) Ethers --  |t Triphenylsilyl (TPS) Ethers --  |t Di-tert-butylmethylsilyl (DTBMS) Ethers --  |t Alkyl Ethers --  |t Methyl Ethers --  |t tert-Butyl Ethers. 
505 8 0 |t Benzyl Ethers (Bn) --  |t p-Methoxybenzyl (PMB) and 3,4-Di-methoxybenzyl (DMB) Ethers --  |t Trityl (Tr) Ethers --  |t Allyl Ethers and Allyloxycarbonyl Derivatives --  |t Alkoxymethyl Ethers --  |t Methoxymethyl (MOM) Ethers --  |t 2-Methoxyethoxymethyl (MEM) Ethers --  |t Benzyloxymethyl (BOM) and Related Ethers --  |t p-Methoxybenzyloxymethyl (PMBM) Ethers --  |t 2-(Trimethylsilyl)ethoxymethyl (SER) Ethers --  |t Tetrahydropyranyl (THP) and Related Ethers --  |t Methylthiomethyl (MTM) Ethers --  |t Esters --  |t Acetate Esters (Ac) --  |t Benzoate Esters (Bz) --  |t Pivalate Esters (R) --  |t Methoxyacetate Esters --  |t Chloroacetate Esters --  |t Levulinate Esters (Lev) --  |t Carbonates --  |t Benzyl Carbonates (RO-CBz) --  |t p-Nitrobenzyl Carbonates (RO-CO[subscript 2]PNB) --  |t tert-Butyl Carbonates (RO-Boc) --  |t 2,2,2-Trichloroethyl Carbonates (RO-Troc) --  |t 2-(Trimethylsilyl)ethyl Carbonates (RO-Teoc) --  |t Allyl Carbonates (RO-Aloc) --  |t General Reviews Concerning the Protection of Hydroxyls --  |t Reviews Concerning Enzyme-Mediated Esterification and Hydrolysis of Esters --  |t Reviews Concerning Organosilicon and Organotin Chemistry Relevant to Hydroxyl Protection --  |t Thiol Protecting Groups --  |t Thioether Derivatives --  |t tert-Butyl Thioethers --  |t Benzyl and Substituted Benzyl Thioethers --  |t Trityl (Tr) Thioethers --  |t 2-(Trimethylsilyl)ethyl (TMSE) Thioethers --  |t 2-Cyanoethyl Thioethers --  |t 9-Fluorenylmethyl (Fm) Thioethers --  |t Thiocarbonate Derivatives --  |t Disulfides as Protecting Groups and Targets --  |t Reviews Concerning the Protection of Thiols --  |t Reviews Concerning the Chemistry of Thiols and Disulfides. 
505 8 0 |t Carboxyl Protecting Groups --  |t General Comments on the Esterification of Carboxylic Acids --  |t Methyl Esters and Derivatives --  |t Methyl Esters --  |t tert-Butyl Esters --  |t Benzyl Esters --  |t Allyl Esters --  |t Phenacyl Esters --  |t Alkoxyalkyl Esters --  |t Esters Cleaved by [beta]-Elimination Reactions --  |t 2,2,2-Trichloroethyl Esters --  |t 2-(Trimethylsilyl)ethyl (TMSE) Esters --  |t 2-Tosylethyl Esters and Related Base-Labile Groups --  |t Silyl Esters --  |t Reviews Concerning the Specific Use of Esters as Protecting Groups --  |t Reviews Concerning the Preparation of Esters --  |t Reviews Concerning Techniques for Facilitating Esterification --  |t Reviews Concerning the Use of Allyl Esters in Carboxyl Protection --  |t Reviews Concerning the Nucleophilic Cleavage of Esters --  |t Phosphate Protecting Groups --  |t The Reaction of Phosphate Esters with Nucleophiles --  |t Alkyl Esters --  |t Methyl and Isopropyl Esters --  |t tert-Butyl Esters --  |t Benzyl Esters --  |t Allyl Esters --  |t 3',5'-Dimethoxybenzoin Esters --  |t p-Hydroxyphenacyl Esters --  |t Esters Cleaved by [beta]-Elimination Reactions --  |t 2-Cyanoethyl Esters --  |t 9-Fluorenylmethyl Esters --  |t 2-(Trimethylsilyl)ethyl Esters --  |t 2-(Methylsulfonyl)ethyl Esters and Related Base-Labile Groups --  |t 2,2,2-Trichloroethyl Esters --  |t Reviews Concerning Protection for the Phosphate Group --  |t Reviews Concerning the Mechanism of Nucleophilic Substitution in Phosphate Esters --  |t Amino Protecting Groups --  |t Imides and Amides --  |t Phthaloyl (Phth) and Tetrachlorophthaloyl (TCP) --  |t Dithiasuccinyl (Dts) --  |t Trifluoroacetyl --  |t Relay Deprotection of N-Acyl Derivatives. 
505 8 0 |t Carbamates --  |t Methoxy- and Ethoxycarbonyl --  |t tert-Butoxycarbonyl (Boc) --  |t Benzyloxycarbonyl (Z or Cbz) --  |t Allyloxycarbonyl (Aloc) --  |t 9-Fluorenylmethoxycarbonyl (Fmoc) --  |t 2-(Trimethylsilyl)ethoxycarbonyl (Teoc) --  |t 2,2,2-Trichloroethoxycarbonyl (Troc) --  |t Sulfonyl Derivatives --  |t Arylsulfonyl Derivatives --  |t 2-(Trimethylsilyl)ethylsulfonyl (SES) Derivatives --  |t N-Sulfenyl Derivatives --  |t N-Alkyl Derivatives --  |t N, O-Acetals --  |t Triazinanones --  |t Benzyl (Bn) and Diphenylmethyl (Dpm) --  |t Trityl (Tr) and 9-Phenylfluorenyl (PhFl) --  |t Allyl --  |t N-Silyl Derivatives --  |t Imine and Enamine Derivatives --  |t N-Bis(methylthio)methylene --  |t N-Diphenylmethylene --  |t Special Cases --  |t Orthogonal Protecting Groups for the Synthesis of Polyamines --  |t Protecting Groups for Guanidines --  |t Protecting Groups for Indoles, Pyrroles, and Imidazoles --  |t General Reviews on Amino Protecting Groups --  |t Reviews Concerning N-Protection in the Synthesis of [alpha]-Amino Aldehydes and Ketones --  |t Reviews Concerning N-Protection in the Synthesis of [beta]-Lactams --  |t Reviews Concerning N-Functional Groups Pertinent to Their Role as Protecting Groups --  |t Reviews Concerning the Synthesis of Natural Guanidine Derivatives --  |t Reviews Concerning the Synthesis of Natural Polyamines. 
540 |a Current Copyright Fee: GBP50.00  |c 0.  |5 Uk 
590 |b TAG Physical Holdings 2 
650 0 |a Organic compounds  |x Synthesis.  |0 http://id.loc.gov/authorities/subjects/sh85023025 
650 0 |a Protective groups (Chemistry)  |0 http://id.loc.gov/authorities/subjects/sh85107650 
650 6 |a Composés organiques  |x Synthèse. 
650 6 |a Groupements protecteurs (Chimie) 
650 7 |a Organic compounds  |x Synthesis.  |2 fast  |0 (OCoLC)fst01047668 
650 7 |a Protective groups (Chemistry)  |2 fast  |0 (OCoLC)fst01079661 
650 7 |a Organische Chemie  |2 gnd 
650 7 |a Schutzgruppe  |2 gnd 
650 7 |a Organische Synthese  |2 gnd 
650 1 7 |a Synthese (chemie)  |2 gtt 
650 1 7 |a Hydroxyl.  |2 gtt 
650 1 7 |a Carbonyl.  |2 gtt 
650 1 7 |a Afscherming.  |2 gtt 
650 1 7 |a Organische verbindingen.  |2 gtt 
650 1 7 |a Carboxylgroepen.  |2 gtt 
650 1 7 |a Aminogroepen.  |2 gtt 
758 |i has work:  |a Protecting groups (Text)  |1 https://id.oclc.org/worldcat/entity/E39PCFYk46bbfgBpprRWTFfqry  |4 https://id.oclc.org/worldcat/ontology/hasWork 
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938 |a Otto Harrassowitz  |b HARR  |n har030120412 
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994 |a 92  |b TAG 
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998 f f |a QD262 .K59 2004  |t 0  |l Galveston Stacks