Verfügbarkeit: Comprehensive organic name reactions and reagents

Comprehensive organic name reactions and reagents: 3

Gespeichert in:

Bibliographische Detailangaben
1. Verfasser:	Wang, Zerong (VerfasserIn)
Format:	Buch
Sprache:	English
Veröffentlicht:	Hoboken, NJ Wiley (2009)
Online-Zugang:	Inhaltsverzeichnis
Beschreibung:	XLIX S., S. 2293 - 3661 Ill., graph. Darst.
ISBN:	9780470533468

Internformat

MARC


LEADER	00000nam a2200000 cc4500
001	BV035650895
003	DE-604
005	20090813
007	t
008	090728s2009 ad\|\| \|\|\|\| 00\|\|\| eng d
020			\|a 9780470533468 \|9 978-0-470-53346-8
035			\|a (OCoLC)635300893
035			\|a (DE-599)BVBBV035650895
040			\|a DE-604 \|b ger \|e rakwb
041	0		\|a eng
049			\|a DE-29T \|a DE-703 \|a DE-19 \|a DE-11
084			\|a VK 5500 \|0 (DE-625)147401:253 \|2 rvk
084			\|a VK 6000 \|0 (DE-625)147413:253 \|2 rvk
084			\|a VK 6003 \|0 (DE-625)147413:256 \|2 rvk
100	1		\|a Wang, Zerong \|e Verfasser \|4 aut
245	1	0	\|a Comprehensive organic name reactions and reagents \|n 3 \|c Zerong Wang
264		1	\|a Hoboken, NJ \|b Wiley \|c (2009)
300			\|a XLIX S., S. 2293 - 3661 \|b Ill., graph. Darst.
336			\|b txt \|2 rdacontent
337			\|b n \|2 rdamedia
338			\|b nc \|2 rdacarrier
773	0	8	\|w (DE-604)BV035164063 \|g 3
856	4	2	\|m Digitalisierung UB Bayreuth \|q application/pdf \|u http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=017705492&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA \|3 Inhaltsverzeichnis
999			\|a oai:aleph.bib-bvb.de:BVB01-017705492

Datensatz im Suchindex

_version_	1804139336600387584
adam_text	CONTENTS XXÌ PART THREE 518. Radziszewski Reaction .............................................. 2293 519. Ramberg-Bäcklund Reaction ....................................... 2298 520. Ranev Nickel ....................................................... 2302 XXii CONTENTS 521. Rauhut-Currier Reaction........................................... 2307 522. Reed Reaction ...................................................... 2311 523. Reformatsky Reaction .............................................. 2314 524. Regitz Diazo Transfer .............................................. 2322 525. Reilly-Rickinbottom Rearrangement ................................ 2326 526. Reimer-Tiemann Reaction .......................................... 2329 527. Reissert Compound ................................................ 2335 528. Reissert Indole Synthesis ........................................... 2341 529. Reppe Alkyne Cyclotrimerization ................................... 2345 530. Reppe Carbonylation ............................................... 2352 531. Reppe Cyclization .................................................. 2358 532. Reppe Vinylation ................................................... 2362 533. Retro-Diels-Alder Reaction ......................................... 2367 534. Retro-Ene Reaction ................................................ 2373 535. Retropinacol Rearrangement ....................................... 2378 536. Reverdin Rearrangement ........................................... 2382 537. Rietini Quinoline Synthesis ......................................... 2385 538. RiekeMetal ........................................................ 2388 539. Riemenschneider Reaction .......................................... 2392 540. Riley Oxidation .................................................... 2395 541. Ritter Reaction ..................................................... 2399 542. Robinson Annulation ............................................... 2405 543. Robinson-Gabriel Oxazole Synthesis ................................ 2410 544. Robinson-Schöpf Condensation ..................................... 2414 545. Rosenmund Reaction ............................................... 2418 546. Rosenmund Reduction ............................................. 2421 547. Rosenmund-von Braun Reaction .................................... 2425 548. Rothemund Reaction ............................................... 2429 549. Roush Crotylboration .............................................. 2435 550. Rowe Rearrangement .............................................. 2439 551. Rubottom Oxidation ................................................ 2442 552. Ruff Degradation ................................................... 2446 CONTENTS ХХШ 553. Rupe Rearrangement ............................................... 2450 554. Sabatier-Senderens Reduction ...................................... 2454 555. Saegusa Cyclization ................................................ 2458 556. Saegusa Oxidation .................................................. 2462 557. Sandmeyer Isatin Synthesis......................................... 2467 558. Sandmeyer Reaction ................................................ 2471 559. Sarett Oxidation ................................................... 2476 560. SaytzeffRule ....................................................... 2480 561. Schiff Base ......................................................... 2484 562. Schlack-Kumpf Reaction ........................................... 2488 563. Schiotterbeck Reaction ............................................. 2491 564. Schmidlin Ketene Synthesis ......................................... 2495 565. Schmidt Glycosylation .............................................. 2498 566. Schmidt Reaction .................................................. 2503 567. Schmidt-Rutz Reaction ............................................. 2511 568. Schmittel Cyclization ............................................... 2514 569. Scholl Reaction ..................................................... 2518 570. Schöllkopf Bis-Lactim Ether Method ................................ 2523 571. Schöllkopf Oxazole Synthesis ....................................... 2529 572. Schönberg Rearrangement ......................................... 2533 573. Schotten-Baumann Reaction ........................................ 2536 574. Schwartz Reagent .................................................. 2540 575. Screttas Lithiation .................................................. 2544 576. Selenoxide Elimination ............................................. 2548 577. Semmler-Wolff Aromatization ...................................... 2552 578. Serini Reaction ..................................................... 2556 579. Seyferth-Gilbert Homologation ..................................... 2559 580. Shapiro Reaction ................................................... 2563 581. Sharpless Aminohydroxylation ...................................... 2568 582. Sharpless Dihydroxylation .......................................... 2574 583. Sharpless Epoxidation .............................................. 2580 584. Shechter-Kaplan Oxidative Nitration ................................ 2586 XXIV CONTENTS 585. Shi Epoxidation .................................................... 2590 586. Simmons-Smith Reaction ........................................... 2594 587. Simonini Reaction .................................................. 2600 588. Skraup Reaction ................................................... 2603 589. Smiles Rearrangement .............................................. 2609 590. Sommelet Reaction ................................................. 2615 591. Sommelet-Hauser Rearrangement .................................. 2620 592. Sonn-Miiller Reaction .............................................. 2625 593. Sonogashira Coupling .............................................. 2628 594. Staudinger [2+2] Cycloaddition ..................................... 2636 595. Staudinger Reaction ................................................ 2642 596. Stec Reaction ...................................................... 2647 597. Steglich Catalyst ................................................... 2651 598. Steglich Rearrangement ............................................ 2656 599. Stephen Reaction ................................................... 2659 600. Stetter Reaction .................................................... 2663 601. Stevens Rearrangement ............................................. 2668 602. Stieglitz Rearrangement ............................................ 2673 603. StilleCoupIing ..................................................... 2677 604. Stobbe Condensation ............................................... 2686 605. Stolle-Becker Synthesis ............................................. 2692 606. Stork Reaction ..................................................... 2695 607. Strecker Degradation ............................................... 2701 608. Strecker Reaction .................................................. 2707 609. Strecker Synthesis .................................................. 2710 610. Suárez Cleavage .................................................... 2718 611. Sugasawa Indole Synthesis .......................................... 2722 612. Sugasawa Reaction ................................................. 2726 613. Sundberg Indole Synthesis .......................................... 2730 614. Suzuki Coupling ................................................... 2733 615. Swarts Reaction .................................................... 2744 616. Takai Olefination ................................................... 2748 CONTENTS XXV 617. Tebbe Olefination .................................................. 2753 618. ter Meer Reaction.................................................. 2758 619. Thiele-Winter Acetoxylation........................................ 2762 620. Thorpe-Ziegler Cyclization ......................................... 2766 621. Tiemann Cyanohydrin Amination................................... 2770 622. Tiemann Rearrangement ........................................... 2773 623. Tiffeneau-Demjanov Ring Expansion................................ 2777 624. Tishchenko Reaction ............................................... 2782 625. Traube Purine Synthesis ............................................ 2789 626. Trofimov Reaction .................................................. 2793 627. Trost Desymmetrization............................................ 2797 628. Truce-Smiles Rearrangement ....................................... 2803 629. Tscherniac-Einhorn Reaction ....................................... 2807 630. Tsuji-Trost Reaction ................................................ 2812 631. Twitchell Process ................................................... 2817 632. Tyrer Process ...................................................... 2822 633. Ueno-Stork Cyclization............................................. 2826 634. UgiReaction....................................................... 2830 635. Ulimann Acridine Synthesis ......................................... 2838 636. Ulimann Coupling .................................................. 2842 637. Ulimann Diaryl Ether Synthesis..................................... 2847 638. Urech Cyanohydrin Method ........................................ 2852 639. Urech Hydantoin Synthesis......................................... 2856 640. van Slyke Method .................................................. 2860 641. Varrentrapp Reaction .............................................. 2864 642. Victor Meyer Reaction .............................................. 2868 643. Vilsmeier Formylation .............................................. 2872 644. Vinylcyclopropane Rearrangement .................................. 2880 645. Voigt Reaction ..................................................... 2888 646. von Auwers Rearrangement ........................................ 2892 647. von Braun Cyanogen Bromide Reaction ............................. 2896 648. von Braun Degradation ............................................. 2900 XXV/ CONTENTS 649. von Braun-Rudolf Synthesis ........................................ 2904 650. von Richter Cinnoline Synthesis ..................................... 2908 651. von Richter Reaction ............................................... 2911 652. Vorbrüggen Glycosylation.......................................... 2915 653. Wacker Oxidation .................................................. 2920 654. Wagner-Jauregg Reaction .......................................... 2926 655. Wagner-Meerwein Rearrangement .................................. 2930 656. Walden Inversion................................................... 2937 657. Wallach Rearrangement ............................................ 2942 658. Weerman Reaction ................................................. 2946 659. Weidenhagen Synthesis ............................................. 2951 660. Weinreb Amide Formation.......................................... 2956 661. Weinreb Ketone Synthesis .......................................... 2963 662. Weiss-Cook Condensation .......................................... 2968 663. Weitz-Scheffer Epoxidation ......................................... 2975 664. Wender Indole Synthesis ............................................ 2980 665. Wessely-Moser Rearrangement ..................................... 2983 666. Westphalen Rearrangement ........................................ 2988 667. Wharton Rearrangement ........................................... 2994 668. Wibaut-Arens Alkylation ........................................... 2998 669. Wichterle Reaction ................................................. 3003 670. Widman-Stoermer Synthesis ........................................ 3008 671. Wilkinson s Catalyst ................................................ 3011 672. Willgerodt-Kindler Reaction ........................................ 3018 673. Williamson Ether Synthesis ......................................... 3026 674. Wittig Reaction .................................................... 3031 675. [1,2]-Wittig Rearrangement ......................................... 3043 676. [2,3]-Wittig Rearrangement ......................................... 3049 677. Wohl Degradation .................................................. 3056 678. Wohl-Aue Reaction ................................................. 3060 679. Wöhler Synthesis ................................................... 3064 680. Wohl-Ziegler Bromination .......................................... 3067 CONTENTS XXVii 681. Wolff Rearrangement .............................................. 3073 682. Wolffenstein-Böters Reaction ....................................... 3081 683. Wolff-Kishner Reduction ........................................... 3084 684. Woodward Cis-Hydroxylation ...................................... 3090 685. Wurtz Synthesis .................................................... 3094 686. Wurtz-Fittig Reaction .............................................. 3100 687. Yamada Coupling .................................................. 3105 688. Yamaguchi Esterification ........................................... 3109 689. Zeisel Determination ............................................... 3115 690. Zelinsky-Stadnikoff Reaction ....................................... 3119 691. Zemplén Deacetylation ............................................. 3123 692. Zerewitinoff Determination ......................................... 3129 693. Ziegler Alcohol Synthesis ........................................... 3134 694. Ziegler-Hafner Azulene Synthesis ................................... 3139 695. Ziegler-Natta Polymerization ....................................... 3144 696. Zimmermann Reaction ............................................. 3158 697. Zincke Disulfide Cleavage ........................................... 3163 698. Zincke Nitration ................................................... 3168 699. Zincke Reaction .................................................... 3172 700. Zincke-Suhl Reaction ............................................... 3178 701. Zinke Synthesis .................................................... 3183 APPENDIXES 1. Schematic Reaction Index ......................................... 3197 2. Reaction Type Summary ........................................... 3323 3. Summary of Initial Publications on Named Organic Reactions ... 3341 4. Journal Abbreviation ............................................... 3407 5. The Statistics of Reaction Published Years ........................ 3625 Subject Index ......................................................... 3631
any_adam_object	1
author	Wang, Zerong
author_facet	Wang, Zerong
author_role	aut
author_sort	Wang, Zerong
author_variant	z w zw
building	Verbundindex
bvnumber	BV035650895
classification_rvk	VK 5500 VK 6000 VK 6003
ctrlnum	(OCoLC)635300893 (DE-599)BVBBV035650895
discipline	Chemie / Pharmazie
format	Book
fullrecord	<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01201nam a2200313 cc4500</leader><controlfield tag="001">BV035650895</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">20090813 </controlfield><controlfield tag="007">t</controlfield><controlfield tag="008">090728s2009 ad\|\| \|\|\|\| 00\|\|\| eng d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9780470533468</subfield><subfield code="9">978-0-470-53346-8</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)635300893</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV035650895</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-29T</subfield><subfield code="a">DE-703</subfield><subfield code="a">DE-19</subfield><subfield code="a">DE-11</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">VK 5500</subfield><subfield code="0">(DE-625)147401:253</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">VK 6000</subfield><subfield code="0">(DE-625)147413:253</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">VK 6003</subfield><subfield code="0">(DE-625)147413:256</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Wang, Zerong</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Comprehensive organic name reactions and reagents</subfield><subfield code="n">3</subfield><subfield code="c">Zerong Wang</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Hoboken, NJ</subfield><subfield code="b">Wiley</subfield><subfield code="c">(2009)</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">XLIX S., S. 2293 - 3661</subfield><subfield code="b">Ill., graph. Darst.</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="b">n</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">nc</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="w">(DE-604)BV035164063</subfield><subfield code="g">3</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="m">Digitalisierung UB Bayreuth</subfield><subfield code="q">application/pdf</subfield><subfield code="u">http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=017705492&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA</subfield><subfield code="3">Inhaltsverzeichnis</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-017705492</subfield></datafield></record></collection>
id	DE-604.BV035650895
illustrated	Illustrated
indexdate	2024-07-09T21:42:28Z
institution	BVB
isbn	9780470533468
language	English
oai_aleph_id	oai:aleph.bib-bvb.de:BVB01-017705492
oclc_num	635300893
open_access_boolean
owner	DE-29T DE-703 DE-19 DE-BY-UBM DE-11
owner_facet	DE-29T DE-703 DE-19 DE-BY-UBM DE-11
physical	XLIX S., S. 2293 - 3661 Ill., graph. Darst.
publishDate	2009
publishDateSearch	2009
publishDateSort	2009
publisher	Wiley
record_format	marc
spelling	Wang, Zerong Verfasser aut Comprehensive organic name reactions and reagents 3 Zerong Wang Hoboken, NJ Wiley (2009) XLIX S., S. 2293 - 3661 Ill., graph. Darst. txt rdacontent n rdamedia nc rdacarrier (DE-604)BV035164063 3 Digitalisierung UB Bayreuth application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=017705492&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis
spellingShingle	Wang, Zerong Comprehensive organic name reactions and reagents
title	Comprehensive organic name reactions and reagents
title_auth	Comprehensive organic name reactions and reagents
title_exact_search	Comprehensive organic name reactions and reagents
title_full	Comprehensive organic name reactions and reagents 3 Zerong Wang
title_fullStr	Comprehensive organic name reactions and reagents 3 Zerong Wang
title_full_unstemmed	Comprehensive organic name reactions and reagents 3 Zerong Wang
title_short	Comprehensive organic name reactions and reagents
title_sort	comprehensive organic name reactions and reagents
url	http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=017705492&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA
volume_link	(DE-604)BV035164063
work_keys_str_mv	AT wangzerong comprehensiveorganicnamereactionsandreagents3

Verfügbarkeit

Es ist kein Print-Exemplar vorhanden.

Fernleihe Bestellen Achtung: Nicht im THWS-Bestand! Inhaltsverzeichnis

MARC

Datensatz im Suchindex

Es ist kein Print-Exemplar vorhanden.

Ähnliche Einträge