Best synthetic methods : Organophosphorus (V) chemistry / (Record no. 246945)
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| fixed length control field | 06056cam a2200577Ia 4500 |
| 001 - CONTROL NUMBER | |
| control field | ocn885009092 |
| 003 - CONTROL NUMBER IDENTIFIER | |
| control field | OCoLC |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20190328114808.0 |
| 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 ||||||||||| |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 140722s2015 ne a ob 001 0 eng d |
| 040 ## - CATALOGING SOURCE | |
| Original cataloging agency | UKMGB |
| Language of cataloging | eng |
| Description conventions | pn |
| Transcribing agency | UKMGB |
| Modifying agency | OCLCO |
| -- | N$T |
| -- | YDXCP |
| -- | OPELS |
| -- | OCLCF |
| -- | EBLCP |
| -- | DEBSZ |
| -- | OCLCQ |
| -- | U3W |
| -- | D6H |
| -- | CUY |
| -- | ZCU |
| -- | MERUC |
| -- | ICG |
| -- | DKC |
| 066 ## - CHARACTER SETS PRESENT | |
| Alternate G0 or G1 character set | (S |
| 016 7# - NATIONAL BIBLIOGRAPHIC AGENCY CONTROL NUMBER | |
| Record control number | 016802671 |
| Source | Uk |
| 019 ## - | |
| -- | 897650677 |
| -- | 902830696 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 9780080982243 |
| Qualifying information | (electronic bk.) |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 0080982247 |
| Qualifying information | (electronic bk.) |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| Canceled/invalid ISBN | 9780080982120 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| Canceled/invalid ISBN | 0080982123 |
| 035 ## - SYSTEM CONTROL NUMBER | |
| System control number | (OCoLC)885009092 |
| Canceled/invalid control number | (OCoLC)897650677 |
| -- | (OCoLC)902830696 |
| 050 #4 - LIBRARY OF CONGRESS CALL NUMBER | |
| Classification number | QD305.P46 |
| 072 #7 - SUBJECT CATEGORY CODE | |
| Subject category code | SCI |
| Subject category code subdivision | 013040 |
| Source | bisacsh |
| 082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER | |
| Classification number | 547.07 |
| Edition number | 23 |
| 100 1# - MAIN ENTRY--PERSONAL NAME | |
| Personal name | Timperley, Chris, |
| Relator term | author. |
| 245 10 - TITLE STATEMENT | |
| Title | Best synthetic methods : Organophosphorus (V) chemistry / |
| Medium | [electronic resource] |
| Statement of responsibility, etc. | co-authored and edited by Chris Timperley. |
| 264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
| Place of production, publication, distribution, manufacture | Amsterdam : |
| Name of producer, publisher, distributor, manufacturer | Academic Press, |
| Date of production, publication, distribution, manufacture, or copyright notice | �2015. |
| 300 ## - PHYSICAL DESCRIPTION | |
| Extent | 1 online resource : |
| Other physical details | illustrations |
| 336 ## - CONTENT TYPE | |
| Content type term | text |
| Content type code | txt |
| Source | rdacontent |
| 336 ## - CONTENT TYPE | |
| Content type term | still image |
| Content type code | sti |
| 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 |
| 490 1# - SERIES STATEMENT | |
| Series statement | Best synthetic methods |
| 504 ## - BIBLIOGRAPHY, ETC. NOTE | |
| Bibliography, etc | Includes bibliographical references and index. |
| 588 0# - SOURCE OF DESCRIPTION NOTE | |
| Source of description note | Online resource; title from PDF title page (EBSCO, viewed December 12, 2014). |
| 520 ## - SUMMARY, ETC. | |
| Summary, etc. | Best Synthetic Methods: ORGANOPHOSPHORUS (V) CHEMISTRY provides systematic coverage of the most common classes of pentavalent organophosphorus compounds and reagents (including phosphonyl, phosphoryl, and organophosphates), and allows researchers an easy point of entry into this complex and economically important field. The book follows the Best Synthetic Methods format, containing practical methods, synthetic tips, and shortcuts. Where relevant, articles include toxicity data and historical context for the reactions. Typical analytical and spectroscopic data are also presented to enable scientists to identify key compound characteristics. The book is a valuable companion to research chemists in both academia and industry, summarizing the best practical methods (often originating in difficult-to-access, foreign-language primary literature) in one place. It is ideally suited for those working on industrial applications of these compounds, including insecticides, herbicides, flame retardants, and plasticizers. |
| 505 0# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | Front Cover; Best Synthetic Methods; OTHER VOLUMES IN THE SERIES; Best Synthetic Methods; Copyright; ACKNOWLEDGEMENTS; REFERENCES; 1.4 PHOSPHORUS COMPOUNDS IN LIVING SYSTEMS; 1.5.3 ORGANOPHOSPHORUS PESTICIDES; 1.6 NOMENCLATURE OF ORGANOPHOSPHORUS COMPOUNDS; 1.7 CHIRAL PHOSPHORUS COMPOUNDS AND BIOLOGICAL IMPLICATIONS; 1.8 PHOSPHORUS-CONTAINING PHARMACEUTICALS; 1.9 FIRE RETARDANTS AND FIRE-EXTINGUISHING COMPOUNDS; 1.10 TOXICOLOGY AND MEDICAL TREATMENT OF ORGANOPHOSPHORUS COMPOUNDS; 1.11 FLUOROGENIC NERVE AGENT MIMICS FOR SCREENING FOR IMPROVED BIOSCAVENGERS. |
| 505 8# - FORMATTED CONTENTS NOTE | |
| Linkage | 880-01 |
| Formatted contents note | 2.23 s-alkyl alkylphosphonochloridothiolates r(r2)p(o)cl2.24 alkyl alkylphosphonofluoridates r(r2)p(o)f; 2.25 n-alkyl or n, n-dialkyl alkylphosphonamidofluoridates r(r2 n)p(o)f (x=h or r2 ; 2.26 s-alkyl alkylphosphonofluoridothiolates r(r2)p(o)f; 2.27 alkyl alkylphosphonocyanidates r(r2)p(o)cn; 2.28 alkyl alkylphosphonic acids r(r2)p(o)oh; 2.29 alkylphosphonofluoridic anhydrides r(f)p(o)op(o)(f)r; 2.30 dialkyl dialkylpyrophosphonates r(r2)p(o)op(o)(or2 r; 2.31 n, n-dialkyl-p-alkylphosphonamidic anhydrides r(r2 n)p(o)op(o)(nr2)r. |
| 505 8# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | 2.32 s, s2 dialkyl dialkyldithiopyrophosphonates r(r2)p(o)op(o)(sr2 r2.33 o-alkyl n-alkyl alkylphosphonamidates rp(o)(nr2)or; 2.34 bis(n, n-dialkyl) alkylphosphonodiamidates rp(o)(nr2)2; 2.35 o, s-dialkyl alkylphosphonothiolates rp(o)(or)sr; 2.36 s-alkyl n-alkyl (or n, n-dialkyl) alkylphosphonamidothiolates rp(o)(nr2)sr; 2.37 s, s2 dialkyl alkylphosphonodithiolates rp(o)(sr2)2; references; 3.9 s-alkyl alkylphosphonochloridothiolothionates rs(r2 p(s)cl; 3.13 alkyl alkyl/aryl alkylphosphonothionates ro(r2 p(s)or2 ; 4.9 alkyl phosphorodiisothiocyanatidates rop(o)(ncs)2. |
| 505 8# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | 4.35 trialkyl phosphates (ro)2p(o)or4.39 dialkyl enolphosphates (ro)2p(o)ocrcr2 (perkow reaction); 4.40 dialkyl phosphorazidates (ro)2p(o)n3; 4.41 dialkyl phosphoramidates (ro)2p(o)nr2 (todd-atherton reaction); 4.42 dialkyl n-arylphosphoramidates (ro)2p(o)nhar; 4.43 diaryl phosphoramidates (aro)2p(o)nr2; 4.44 dialkyl n-methyl-n-(phosphoryl)phosphoramidates (ro)2p(o)n(me)p(x)r2; 4.45 dialkyl n-methyl-n-acylphosphoramidates (ro)2p(o)n(me)cor2 4.46 disubstituted n-aryl(or alkyl)-n-chlorophosphoramidates (ro)2p(o)n(cl)ar; 4.47 dialkyl n, n-dihalophosphoramidates (ro)2p(o)nx2 (x=cl or br). |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | Organophosphorus compounds. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | Organophosphorus compounds |
| General subdivision | Synthesis. |
| 650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | SCIENCE |
| General subdivision | Chemistry |
| -- | Organic. |
| Source of heading or term | bisacsh |
| 650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | Organophosphorus compounds. |
| Source of heading or term | fast |
| Authority record control number | (OCoLC)fst01047997 |
| 650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | Organophosphorus compounds |
| General subdivision | Synthesis. |
| Source of heading or term | fast |
| Authority record control number | (OCoLC)fst01048004 |
| 655 #4 - INDEX TERM--GENRE/FORM | |
| Genre/form data or focus term | Electronic books. |
| 655 #7 - INDEX TERM--GENRE/FORM | |
| Genre/form data or focus term | Electronic books. |
| Source of term | lcgft |
| 776 08 - ADDITIONAL PHYSICAL FORM ENTRY | |
| Relationship information | Print version: |
| Main entry heading | Timperley, Chris. |
| Title | Best Synthetic Methods: ORGANOPHOSPHORUS (V) CHEMISTRY. |
| Place, publisher, and date of publication | Burlington : Elsevier Science, �2014 |
| International Standard Book Number | 9780080982120 |
| 830 #0 - SERIES ADDED ENTRY--UNIFORM TITLE | |
| Uniform title | Best synthetic methods. |
| 856 40 - ELECTRONIC LOCATION AND ACCESS | |
| Materials specified | ScienceDirect |
| Uniform Resource Identifier | http://www.sciencedirect.com/science/book/9780080982120 |
| 880 8# - ALTERNATE GRAPHIC REPRESENTATION | |
| Linkage | 505-01/(S |
| a | 1.13 WORKING SAFELY WITH ORGANOPHOSPHORUS COMPOUNDSREFERENCES; 2.5 ALKYLPHOSPHONIC DIFLUORIDES RP(O)F2; 2.9 ALKYLPHOSPHONIC ISOTHIOCYANATOFLUORIDES RP(O)(NCS)F; 2.16 DIALKYL (Sa(B-HYDROXYPHOSPHONATES (RO)2P(O)CH(OH)R2 (PUDOVIK REACTION); 2.17 DIALKYL (Sa(B-SILOXYPHOSPHONATES (RO)2P(O)CH(OSIME3)R2 (ABRAMOV REACTION); 2.18 DIALKYL (Sa(B-AMINOPHOSPHONATES (RO)2P(O)CR2NR2 (KABACHNIK-FIELDS REACTION); 2.19 DIALKYL ALKENYLPHOSPHONATES (RO)2P(O)CCR2; 2.20 DIALKYL ALKYNYLPHOSPHONATES (RO)2P(O)CaCR; 2.22 N, N-DIALKYL ALKYLPHOSPHONAMIDOCHLORIDATES R(R22N)P(O)CL. |
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