Name reactions : (Record no. 580)
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| 000 -LEADER | |
|---|---|
| fixed length control field | 08101cam a2200253 a 4500 |
| 001 - CONTROL NUMBER | |
| control field | 1822 |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20200706102439.0 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 060411s2006 gw a b 001 0 eng |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 9783540300304 (acidfree paper) |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 3540300309 (acidfree paper) |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 9788181286758 |
| 040 ## - CATALOGING SOURCE | |
| Transcribing agency | PK |
| 082 00 - DEWEY DECIMAL CLASSIFICATION NUMBER | |
| Classification number | 547/.2 |
| Edition number | 22 |
| Item number | L69311 |
| 100 1# - MAIN ENTRY--PERSONAL NAME | |
| Personal name | Li, Jie Jack. |
| 245 10 - TITLE STATEMENT | |
| Title | Name reactions : |
| Remainder of title | a collection of detailed reaction mechanisms / |
| Statement of responsibility, etc | Jie Jack Li. |
| 250 ## - EDITION STATEMENT | |
| Edition statement | 3rd expanded ed. |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT) | |
| Place of publication, distribution, etc | New Delhi : |
| Name of publisher, distributor, etc | Springer, |
| Date of publication, distribution, etc | 2007 |
| 300 ## - PHYSICAL DESCRIPTION | |
| Extent | xx, 652 p. |
| Other physical details | ill. ; |
| Dimensions | 24 cm. |
| 500 ## - GENERAL NOTE | |
| General note | includes index |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | Chemical reactions. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | Chemistry, Organic. |
| 942 ## - ADDED ENTRY ELEMENTS (KOHA) | |
| Koha item type | Books |
| 505 0# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | Alder ene reaction;Aldol condensation;Algar-Flynn-Oyamada Reaction;Allan-Robinson reaction;Appel reaction;Arndt-Eistert homologation;Baeyer-Villiger oxidation;Baker-Venkataraman rearrangement;Bamberger rearrangement;Bamford-Stevens reaction;Barbier coupling reaction;Bargellini reaction;Bartoli indole synthesis;Barton radical decarboxylation;Barton-McCombie deoxygenation;Barton nitrite photolysis;Barton-Zard reaction;Batcho-Leimgruber indole synthesis;Baylis-Hillman reaction;Beckmann rearrangement;Beirut reaction;Benzilic acid rearrangement;Benzoin condensation;Bergman cyclization;Biginelli pyrimidone synthesis;Birch reduction;Bischler-Moehlau indole synthesis;Bischler-Napieralski reaction;Blaise reaction;Blanc chloromethylation;Blum aziridine synthesis;Boekelheide reaction;Boger pyridine synthesis;Borch reductive amination;Borsche-Drechsel cyclization;Boulton-Katritzky rearrangement;Bouveault aldehyde synthesis;Bouveault-Blanc reduction;Boyland-Sims oxidation;Bradsher reaction;Brook rearrangement;Brown hydroboration;Bucherer carbazole synthesis;Bucherer reaction;Bucherer-Bergs reaction;Buchner-Curtius-Schlotterbeck reaction;Buchner method of ring expansion;Buchwald-Hartwig C-N and C-O bond formation reactions;Burgess dehydrating reagent;Cadiot-Chodkiewicz coupling;Camps quinolinol synthesis;Cannizzaro disproportionation;Carroll rearrangement;Castro-Stephens coupling;Chan alkyne reduction;Chan-Lam coupling reaction;Chapman rearrangement;Chichibabin pyridine synthesis;Chugaev elimination;Ciamician-Dennsted rearrangement;Claisen condensation;Claisen isoxazole synthesis;Claisen rearrangements;Clemmensen reduction;Combes quinoline synthesis;Conrad-Limpach reaction;Cope elimination reaction;Cope rearrangement;Corey-Bakshi-Shibata (CBS) reduction;Corey-Chaykovsky reaction;Corey-Fuchs reaction;Corey-Kim oxidation;Corey-Nicolaou macrolactonization;Corey-Seebach reaction;Corey-Winter olefin synthesis;Criegee glycol cleavage;Criegee mechanism of ozonolysis;Curtius rearrangement;Dakin oxidation;Dakin-West reaction;Danheiser annulation;Darzens glycidic ester condensation;Davis chiral oxaziridine reagents;Delepine amine synthesis;de Mayo reaction;Demjanov rearrangement;Dess-Martin periodinane oxidation;Dieckmann condensation;Diels-Alder reaction;Dienone-phenol rearrangement;Di-?-methane rearrangement;Doebner quinoline synthesis;Doetz reaction;Dowd-Beckwith ring expansion;Erlenmeyer-Ploechl azlactone synthesis;Eschenmoser-Tanabe fragmentation;Eschweiler-Clarke reductive alkylation of amines;Evans aldol reaction;Favorskii rearrangement and quasi-Favorskii rearrangement;Feist-Benary furan synthesis;Ferrier carbocyclization;Ferrier glycal allylic rearrangement;Fiesselmann thiophene synthesis;Fischer indole synthesis;Fischer oxazole synthesis;Fleming-Kumada oxidation;Friedel-Crafts reaction;Friedlander quinoline synthesis;Fries rearrangement;Fukuyama amine synthesis;Fukuyama reduction;Gabriel synthesis;Gabriel-Colman rearrangement;Gassman indole synthesis;Gattermann-Koch reaction;Gewald aminothiophene synthesis;Glaser coupling;Gomberg-Bachmann reaction;Gould-Jacobs reaction;Grignard reaction;Grob fragmentation;Guareschi-Thorpe condensation;Hajos-Wiechert reaction;Haller-Bauer reaction;Hantzsch dihydropyridine synthesis;Hantzsch pyrrole synthesis;Heck reaction;Hegedus indole synthesis;Hell-Volhard-Zelinsky reaction;Henry nitroaldol reaction;Hinsberg synthesis of thiophene derivatives;Hiyama cross-coupling reaction;Hofmann rearrangement;Hofmann-Loeffler-Freytag reaction;Horner-Wadsworth-Emmons reaction;Houben-Hoesch reaction;Hunsdiecker-Borodin reaction;Hurd-Mori 1,2,3-thiadiazole synthesis;Jacobsen-Katsuki epoxidation;Japp-Klingemann hydrazone synthesis;Jones oxidation;Julia-Kocienski olefination;Julia-Lythgoe olefination;Kahne-Crich glycosidation;Keck macrolactonization;Knoevenagel condensation;Knorr pyrazole synthesis;Koch-Haaf carbonylation;Koenig-Knorr glycosidation;Kolbe-Schmitt reaction;Kostanecki reaction;Kroehnke pyridine synthesis;Kumada cross-coupling reaction;Lawesson's reagent;Leuckart-Wallach reaction;Lossen rearrangement;McFadyen-Stevens reduction;McMurry coupling;MacMillan catalyst;Mannich reaction;Marshall boronate fragmentation;Martin's sulfurane dehydrating reagent;Masamune-Roush conditions;Meerwein-Ponndorf-Verley reduction;Meisenheimer complex;[1,2]-Meisenheimer rearrangement;[2,3]-Meisenheimer rearrangement;Meth-Cohn quinoline synthesis;Meyers oxazoline method;Meyer-Schuster rearrangement;Michael addition;Michaelis-Arbuzov phosphonate synthesis;Midland reduction;Mislow-Evans rearrangement;Mitsunobu reaction;Miyaura borylation;Moffatt oxidation;Montgomery coupling;Morgan-Walls reaction;Mori-Ban indole synthesis;Mukaiyama aldol reaction;Mukaiyama Michael addition;Mukaiyama reagent;Myers-Saito cyclization;Nazarov cyclization;Neber rearrangement;Nef reaction;Negishi cross-coupling reaction;Nenitzescu indole synthesis;Nicholas reaction;Nicolaou dehydrogenation;Nicolaou hydroxy-dithioketal cyclization;Nicolaou hydroxy-ketone reductive cyclic ether formation;Nicolaou oxyselenation;Noyori asymmetric hydrogenation;Nozaki-Hiyama-Kishi reaction;Oppenauer oxidation;Overman rearrangement;Paal thiophene synthesis;Paal-Knorr furan synthesis;Parham cyclization;Passerini reaction;Paterno-Buchi reaction;Pauson-Khand cyclopentenone synthesis;Payne rearrangement;Pechmann coumarin synthesis;Perkin reaction;Petasis reaction;Peterson olefination;Pictet-Gams isoquinoline synthesis;Pictet-Spengler tetrahydroisoquinoline synthesis;Pinacol rearrangement;Pinner reaction;Polonovski reaction;Polonovski-Potier reaction;Pomeranz-Fritsch reaction;Prevost trans-dihydroxylation;Prins reaction;Pschorr cyclization;Pummerer rearrangement;Ramberg-Backlund reaction;Reformatsky reaction;Regitz diazo synthesis;Reimer-Tiemann reaction;Reissert aldehyde synthesis;Reissert indole synthesis;Ring-closing metathesis (RCM);Ritter reaction;Robinson annulation;Robinson-Gabriel synthesis;Robinson-Schoepf reaction;Rosenmund reduction;Rubottom oxidation;Rupe rearrangement;Saegusa oxidation;Sakurai allylation reaction;Sandmeyer reaction;Schiemann reaction;Schmidt reaction;Schmidt's trichloroacetimidate glycosidation reaction;Shapiro reaction;Sharpless asymmetric amino hydroxylation;Sharpless asymmetric epoxidation;Sharpless asymmetric dihydroxylation;Sharpless olefin synthesis;Simmons-Smith reaction;Skraup quinoline synthesis;Smiles rearrangement;Sommelet reaction;Sommelet-Hauser rearrangement;Sonogashira reaction;Staudinger ketene cycloaddition;Staudinger reduction;Sternbach benzodiazepine synthesis;Stetter reaction;Still-Gennari phosphonate reaction;Stille coupling;Stille-Kelly reaction;Stobbe condensation;Stork enamine reaction;Strecker amino acid synthesis;Suzuki coupling;Swern oxidation;Takai iodoalkene synthesis;Tebbe olefination;TEMPO-mediated oxidation;Thorpe-Ziegler reaction;Tsuji-Trost reaction;Ugi reaction;Ullmann reaction;van Leusen oxazole synthesis;Vilsmeier-Haack reaction;Vilsmeier mechanism for acid chloride formation;Vinylcyclopropane-cyclopentene rearrangement;von Braun reaction;Wacker oxidation;Wagner-Meerwein rearrangement;Weiss-Cook reaction;Wharton oxygen transposition reaction;Willgerodt-Kindler reaction;Wittig reaction;[1,2]-Wittig rearrangement;[2,3]-Wittig rearrangement;Wohl-Ziegler reaction;Wolff rearrangement;Wolff-Kishner reduction;Yamaguchi esterification;Zincke reaction. |
| Withdrawn status | Damaged status | Not for loan | Home library | Current library | Date acquired | Source of acquisition | Full call number | Barcode | Date last seen | Price effective from | Koha item type |
|---|---|---|---|---|---|---|---|---|---|---|---|
| UE-Central Library | UE-Central Library | 08.06.2018 | U.E. | 547.2 L69311 | T1822 | 16.05.2019 | 08.06.2018 | Books |
