Name reactions a collection of detailed reaction mechanisms

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1. Verfasser:	Li, Jie Jack 1964- (VerfasserIn)
Format:	Buch
Sprache:	English
Veröffentlicht:	Berlin [u.a.] Springer 2006
Ausgabe:	3., expanded ed.
Schlagworte:	Composés organiques - Synthèse Réactions chimiques organiques - Mécanismes Chemical reactions Chemistry, Organic Reaktionsmechanismus Namensreaktion Organische Chemie Wörterbuch
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650		4	\|a Chemistry, Organic
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Datensatz im Suchindex

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adam_text	Table of Contents Abbreviations XVIII Alder ene reaction 1 Aldol condensation 3 Algar Flynn Oyamada reaction 5 Allan Robinson reaction 8 Appel reaction 10 Arndt Eistert homologation 12 Baeyer Villiger oxidation 14 Baker Venkataraman rearrangement 16 Bamberger rearrangement 18 Bamford Stevens reaction 20 Barbier coupling reaction 22 Bargellini reaction 24 Bartoli indole synthesis 26 Barton radical decarboxylation 28 Barton McCombie deoxygenation 30 Barton nitrite photolysis 32 Barton Zard reaction 34 Batcho Leimgruber indole synthesis 36 Baylis Hillman reaction 39 Beckmann rearrangement 41 Beirut reaction 43 Benzilic acid rearrangement 45 Benzoin condensation 47 Bergman cyclization 49 Biginelli pyrimidone synthesis 51 Birch reduction 53 Bischler Mohlau indole synthesis 55 Bischler Napieralski reaction 57 Blaise reaction 59 Blanc chloromethylation 61 Blum aziridine synthesis 63 Boekelheide reaction 65 Boger pyridine synthesis 67 Borch reductive amination 69 Borsche Drechsel cyclization 71 Boulton Katritzky rearrangement 73 Bouveault aldehyde synthesis 75 Bouveault Blanc reduction 77 Boyland Sims oxidation 79 Bradsher reaction 81 Brook rearrangement 83 Brown hydroboration 85 XII Bucherer carbazole synthesis 87 Bucherer reaction 90 Bucherer Bergs reaction 92 BUchner Curtius Schlotterbeck reaction 94 Biichner method of ring expansion 96 Buchwald Hartwig C N bond and C O bond formation reactions 98 Burgess dehydrating reagent 100 Cadiot Chodkiewicz coupling 102 Camps quinolinol synthesis 104 Cannizzaro dispropotionation 107 Carroll rearrangement 109 Castro Stephens coupling 112 Chan alkyne reduction 114 Chan Lam coupling reaction 116 Chapman rearrangement 118 Chichibabin pyridine synthesis 120 Chugaev reaction 123 Ciamician Dennsted rearrangement 125 Claisen condensation 127 Claisen isoxazole synthesis 129 Claisen rearrangement 131 Abnormal Claisen rearrangement 133 Eschenmoser Claisen amide acetal rearrangement 135 Ireland Claisen (silyl ketene acetal) rearrangement 137 Johnson Claisen (orthoester) rearrangement 139 Clemmensen reduction 141 Combes quinoline synthesis 144 Conrad Limpach reaction 147 Cope elimination reaction 149 Cope rearrangement 151 Oxy Cope rearrangement 152 Anionic oxy Cope rearrangement 153 Corey Bakshi Shibata (CBS) reduction 154 Corey Chaykovsky reaction 157 Corey Fuchs reaction 160 Corey Kim oxidation 162 Corey Nicolaoumacrolactonization 164 Corey Seebach dithiane reaction 166 Corey Winter olefin synthesis 168 Criegee glycol cleavage 171 Criegee mechanism of ozonolysis 173 Curtius rearrangement 175 Dakin oxidation 177 Dakin West reaction 179 Danheiser annulation 181 Darzens glycidic ester condensation 183 XIII Davis chiral oxaziridine reagent 185 Delepine amine synthesis 187 de Mayo reaction 189 Demjanov rearrangement 191 Tiffeneau Demjanov rearrangement 193 Dess Martin oxidation 195 Dieckmann condensation 197 Diels Alder reaction 199 Dienone phenol rearrangement 202 Di 7t methane rearrangement 204 Doebner quinoline synthesis 206 Dotz reaction 208 Dowd Beckwith ring expansion 210 Erlenmeyer Plochl azlactone synthesis 212 Eschenmoser Tanabe fragmentation 214 Eschweiler Clarke reductive alkylation of amines 216 Evans aldol reaction 218 Favorskii rearrangement and quasi Favorskii rearrangement 220 Feist Benary furan synthesis 222 Ferrier carbocyclization 224 Ferrier glycal allylic rearrangement 227 Fiesselmann thiophene synthesis 230 Fischer indole synthesis 233 Fischer oxazole synthesis 235 Fleming Tamao oxidation 237 Tamao Kumada oxidation 239 Friedel Crafts reaction 240 Friedlander quinoline synthesis 243 Fries rearrangement 245 Fukuyama amine synthesis 247 Fukuyama reduction 249 Gabriel synthesis 251 Ing Manske procedure 253 Gabriel Colman rearrangement 255 Gassman indole synthesis 257 Gattermann Koch reaction 259 Gewald aminothiophene synthesis 261 Glaser coupling 263 Eglinton coupling 265 Gomberg Bachmann reaction 267 Gould Jacobs reaction 269 Grignard reaction 271 Grab fragmentation 273 Guareschi Thorpe condensation 275 Hajos Wiechert reaction 277 Haller Bauer reaction 279 XIV Hantzsch dihydropyridine synthesis 281 Hantzsch pyrrole synthesis 283 Heck reaction 285 Heteroaryl Heck reaction 287 Hegedus indole synthesis 289 Hell Volhard Zelinsky reaction 291 Henry nitroaldol reaction 293 Hinsberg synthesis of thiophene derivatives 295 Hiyama cross coupling reaction 297 Hiyama Denmark cross coupling reaction 299 Hofmann rearrangement 302 Hofmann Loffler Freytag reaction 304 Horner Wadsworth Emmons reaction 306 Houben Hoesch synthesis 308 Hunsdiecker Borodin reaction 310 Hurd Mori 1,2,3 thiadiazole synthesis 312 Jacobsen Katsuki epoxidation 314 Japp Klingemann hydrazone synthesis 316 Jones oxidation 318 Julia Kocienski olefination 321 Julia Lythgoe olefination 323 Kahne Crich glycosidation 325 Keck macrolactonization 327 Knoevenagel condensation 329 Knorr pyrazole synthesis 331 Paal Knorr pyrrole synthesis 333 Koch Haaf carbonylation 335 Koenig Knorr glycosidation 337 Kolbe Schmitt reaction 339 Kostanecki reaction 341 Krohnke pyridine synthesis 343 Kumada cross coupling reaction 345 Lawesson's reagent 348 Leuckart Wallach reaction 350 Lossen rearrangement 352 McFadyen Stevens reduction 354 McMurry coupling 356 MacMillan catalyst 358 Mannich reaction 361 Marshall boronate fragmentation 363 Martin's sulfurane dehydrating reagent 365 Masamune Roush conditions 367 Meerwein Ponndorf Verley reduction 369 Meisenheimer complex 371 [1,2] Meisenheimer rearrangement 372 [2,3] Meisenheimer rearrangement 374 XV Meth Cohn quinoline synthesis 376 Meyers oxazoline method 378 Meyer Schuster rearrangement 380 Michael addition 382 Michaelis Arbuzov phosphonate synthesis 384 Midland reduction 386 Mislow Evans rearrangement 388 Mitsunobu reaction 390 Miyaura borylation 392 Moffatt oxidation 394 Montgomery coupling 396 Morgan Walls reaction 399 Pictet Hubert reaction 400 Mori Ban indole synthesis 401 Mukaiyama aldol reaction 403 Mukaiyama Michael addition 405 Mukaiyama reagent 406 Myers Saito cyclization 408 Nazarov cyclization 410 Neber rearrangement 412 Nef reaction 414 Negishi cross coupling reaction 416 Nenitzescu indole synthesis 418 Nicholas reaction 420 Nicolaou dehydrogenation 422 Nicolaou hydroxy dithioketal cyclization 424 Nicolaou hydroxy ketone reductive cyclic ether formation 426 Nicolaou oxyselenation 428 Noyori asymmetric hydrogenation 430 Nozaki Hiyama Kishi reaction 432 Oppenauer oxidation 434 Overman rearrangement 436 Paal thiophene synthesis 438 Paal Knorr furan synthesis 440 Parham cyclization 442 Passerini reaction 444 Paterno Biichi reaction 446 Pauson Khand cyclopentenone synthesis 448 Payne rearrangement 450 Pechmann coumarin synthesis 452 Perkin reaction 454 Petasis reaction 456 Peterson olefination 458 Pictet Gams isoquinoline synthesis 460 Pictet Spengler tetrahydroisoquinoline synthesis 462 Pinacol rearrangement 464 XVI Pinner reaction 466 Polonovski reaction 468 Polonovski Potier rearrangement 470 Pomeranz Fritsch reaction 472 Schlittler Miiller modification 473 Prevost frans dihydroxylation 475 Woodward cw dihydroxylation 476 Prins reaction 478 Pschorr cyclization 480 Pummerer rearrangement 483 Ramberg Backlund reaction 485 Reformatsky reaction 487 Regitz diazo synthesis 489 Reimer Tiemann reaction 492 Reissert aldehyde synthesis 494 Reissert indole synthesis 497 Ring closing metathesis 499 Ritter reaction 501 Robinson annulation 503 Robinson Gabriel synthesis 505 Robinson Schopf reaction 507 Rosenmund reduction 509 Rubottom oxidation 511 Rupe rearrangement 513 Saegusa oxidation 515 Sakurai allylation reaction 518 Sandmeyer reaction 520 Schiemann reaction 522 Schmidt reaction 524 Schmidt's trichloroacetimidate glycosidation reaction 526 Shapiro reaction 529 Sharpless asymmetric amino hydroxylation 531 Sharpless asymmetric epoxidation 533 Sharpless asymmetric dihydroxylation 536 Sharpless olefin synthesis 540 Simmons Smith reaction 543 Skraup quinoline synthesis 545 Doebner von Miller reaction 547 Smiles rearrangement 549 Newman Kwart reaction 551 Truce Smile rearrangement 553 Sommelet reaction 555 Sommelet Hauser rearrangement 557 Sonogashira reaction 559 Staudinger ketene cycloaddition 561 Staudinger reduction 563 XVII Stembach benzodiazepine synthesis 565 Stetter reaction 567 Still Gennari phosphonate reaction 569 Stille coupling 571 Stille Kelly reaction 573 Stobbe condensation 575 Stork enamine reaction 577 Strecker amino acid synthesis 579 Suzuki coupling 581 Swern oxidation 583 Takai iodoalkene synthesis 585 Tebbe olefmation 587 Petasis alkenylation 587 TEMPO mediated oxidation 589 Thorpe Ziegler reaction 592 Tsuji Trost allylation 594 Ugi reaction 596 Ullmann reaction 599 van Leusen oxazole synthesis 601 Vilsmeier Haack reaction 603 Vilsmeier mechanism for acid chloride formation 605 Vinylcyclopropane cyclopentene rearrangement 606 von Braun reaction 608 Wacker oxidation 610 Wagner Meerwein rearrangement 612 Weiss Cook reaction 614 Wharton oxygen transposition reaction 616 Willgerodt Kindler reaction 618 Wittig reaction 621 Schlosser modification of the Wittig reaction 622 [1,2] Wittig rearrangement 624 [2,3] Wittig rearrangement 626 Wohl Ziegler reaction 628 Wolff rearrangement 630 Wolff Kishner reduction 632 Yamaguchi esterification 634 Zincke reaction 637 Subject Index 641
adam_txt	Table of Contents Abbreviations XVIII Alder ene reaction 1 Aldol condensation 3 Algar Flynn Oyamada reaction 5 Allan Robinson reaction 8 Appel reaction 10 Arndt Eistert homologation 12 Baeyer Villiger oxidation 14 Baker Venkataraman rearrangement 16 Bamberger rearrangement 18 Bamford Stevens reaction 20 Barbier coupling reaction 22 Bargellini reaction 24 Bartoli indole synthesis 26 Barton radical decarboxylation 28 Barton McCombie deoxygenation 30 Barton nitrite photolysis 32 Barton Zard reaction 34 Batcho Leimgruber indole synthesis 36 Baylis Hillman reaction 39 Beckmann rearrangement 41 Beirut reaction 43 Benzilic acid rearrangement 45 Benzoin condensation 47 Bergman cyclization 49 Biginelli pyrimidone synthesis 51 Birch reduction 53 Bischler Mohlau indole synthesis 55 Bischler Napieralski reaction 57 Blaise reaction 59 Blanc chloromethylation 61 Blum aziridine synthesis 63 Boekelheide reaction 65 Boger pyridine synthesis 67 Borch reductive amination 69 Borsche Drechsel cyclization 71 Boulton Katritzky rearrangement 73 Bouveault aldehyde synthesis 75 Bouveault Blanc reduction 77 Boyland Sims oxidation 79 Bradsher reaction 81 Brook rearrangement 83 Brown hydroboration 85 XII Bucherer carbazole synthesis 87 Bucherer reaction 90 Bucherer Bergs reaction 92 BUchner Curtius Schlotterbeck reaction 94 Biichner method of ring expansion 96 Buchwald Hartwig C N bond and C O bond formation reactions 98 Burgess dehydrating reagent 100 Cadiot Chodkiewicz coupling 102 Camps quinolinol synthesis 104 Cannizzaro dispropotionation 107 Carroll rearrangement 109 Castro Stephens coupling 112 Chan alkyne reduction 114 Chan Lam coupling reaction 116 Chapman rearrangement 118 Chichibabin pyridine synthesis 120 Chugaev reaction 123 Ciamician Dennsted rearrangement 125 Claisen condensation 127 Claisen isoxazole synthesis 129 Claisen rearrangement 131 Abnormal Claisen rearrangement 133 Eschenmoser Claisen amide acetal rearrangement 135 Ireland Claisen (silyl ketene acetal) rearrangement 137 Johnson Claisen (orthoester) rearrangement 139 Clemmensen reduction 141 Combes quinoline synthesis 144 Conrad Limpach reaction 147 Cope elimination reaction 149 Cope rearrangement 151 Oxy Cope rearrangement 152 Anionic oxy Cope rearrangement 153 Corey Bakshi Shibata (CBS) reduction 154 Corey Chaykovsky reaction 157 Corey Fuchs reaction 160 Corey Kim oxidation 162 Corey Nicolaoumacrolactonization 164 Corey Seebach dithiane reaction 166 Corey Winter olefin synthesis 168 Criegee glycol cleavage 171 Criegee mechanism of ozonolysis 173 Curtius rearrangement 175 Dakin oxidation 177 Dakin West reaction 179 Danheiser annulation 181 Darzens glycidic ester condensation 183 XIII Davis chiral oxaziridine reagent 185 Delepine amine synthesis 187 de Mayo reaction 189 Demjanov rearrangement 191 Tiffeneau Demjanov rearrangement 193 Dess Martin oxidation 195 Dieckmann condensation 197 Diels Alder reaction 199 Dienone phenol rearrangement 202 Di 7t methane rearrangement 204 Doebner quinoline synthesis 206 Dotz reaction 208 Dowd Beckwith ring expansion 210 Erlenmeyer Plochl azlactone synthesis 212 Eschenmoser Tanabe fragmentation 214 Eschweiler Clarke reductive alkylation of amines 216 Evans aldol reaction 218 Favorskii rearrangement and quasi Favorskii rearrangement 220 Feist Benary furan synthesis 222 Ferrier carbocyclization 224 Ferrier glycal allylic rearrangement 227 Fiesselmann thiophene synthesis 230 Fischer indole synthesis 233 Fischer oxazole synthesis 235 Fleming Tamao oxidation 237 Tamao Kumada oxidation 239 Friedel Crafts reaction 240 Friedlander quinoline synthesis 243 Fries rearrangement 245 Fukuyama amine synthesis 247 Fukuyama reduction 249 Gabriel synthesis 251 Ing Manske procedure 253 Gabriel Colman rearrangement 255 Gassman indole synthesis 257 Gattermann Koch reaction 259 Gewald aminothiophene synthesis 261 Glaser coupling 263 Eglinton coupling 265 Gomberg Bachmann reaction 267 Gould Jacobs reaction 269 Grignard reaction 271 Grab fragmentation 273 Guareschi Thorpe condensation 275 Hajos Wiechert reaction 277 Haller Bauer reaction 279 XIV Hantzsch dihydropyridine synthesis 281 Hantzsch pyrrole synthesis 283 Heck reaction 285 Heteroaryl Heck reaction 287 Hegedus indole synthesis 289 Hell Volhard Zelinsky reaction 291 Henry nitroaldol reaction 293 Hinsberg synthesis of thiophene derivatives 295 Hiyama cross coupling reaction 297 Hiyama Denmark cross coupling reaction 299 Hofmann rearrangement 302 Hofmann Loffler Freytag reaction 304 Horner Wadsworth Emmons reaction 306 Houben Hoesch synthesis 308 Hunsdiecker Borodin reaction 310 Hurd Mori 1,2,3 thiadiazole synthesis 312 Jacobsen Katsuki epoxidation 314 Japp Klingemann hydrazone synthesis 316 Jones oxidation 318 Julia Kocienski olefination 321 Julia Lythgoe olefination 323 Kahne Crich glycosidation 325 Keck macrolactonization 327 Knoevenagel condensation 329 Knorr pyrazole synthesis 331 Paal Knorr pyrrole synthesis 333 Koch Haaf carbonylation 335 Koenig Knorr glycosidation 337 Kolbe Schmitt reaction 339 Kostanecki reaction 341 Krohnke pyridine synthesis 343 Kumada cross coupling reaction 345 Lawesson's reagent 348 Leuckart Wallach reaction 350 Lossen rearrangement 352 McFadyen Stevens reduction 354 McMurry coupling 356 MacMillan catalyst 358 Mannich reaction 361 Marshall boronate fragmentation 363 Martin's sulfurane dehydrating reagent 365 Masamune Roush conditions 367 Meerwein Ponndorf Verley reduction 369 Meisenheimer complex 371 [1,2] Meisenheimer rearrangement 372 [2,3] Meisenheimer rearrangement 374 XV Meth Cohn quinoline synthesis 376 Meyers oxazoline method 378 Meyer Schuster rearrangement 380 Michael addition 382 Michaelis Arbuzov phosphonate synthesis 384 Midland reduction 386 Mislow Evans rearrangement 388 Mitsunobu reaction 390 Miyaura borylation 392 Moffatt oxidation 394 Montgomery coupling 396 Morgan Walls reaction 399 Pictet Hubert reaction 400 Mori Ban indole synthesis 401 Mukaiyama aldol reaction 403 Mukaiyama Michael addition 405 Mukaiyama reagent 406 Myers Saito cyclization 408 Nazarov cyclization 410 Neber rearrangement 412 Nef reaction 414 Negishi cross coupling reaction 416 Nenitzescu indole synthesis 418 Nicholas reaction 420 Nicolaou dehydrogenation 422 Nicolaou hydroxy dithioketal cyclization 424 Nicolaou hydroxy ketone reductive cyclic ether formation 426 Nicolaou oxyselenation 428 Noyori asymmetric hydrogenation 430 Nozaki Hiyama Kishi reaction 432 Oppenauer oxidation 434 Overman rearrangement 436 Paal thiophene synthesis 438 Paal Knorr furan synthesis 440 Parham cyclization 442 Passerini reaction 444 Paterno Biichi reaction 446 Pauson Khand cyclopentenone synthesis 448 Payne rearrangement 450 Pechmann coumarin synthesis 452 Perkin reaction 454 Petasis reaction 456 Peterson olefination 458 Pictet Gams isoquinoline synthesis 460 Pictet Spengler tetrahydroisoquinoline synthesis 462 Pinacol rearrangement 464 XVI Pinner reaction 466 Polonovski reaction 468 Polonovski Potier rearrangement 470 Pomeranz Fritsch reaction 472 Schlittler Miiller modification 473 Prevost frans dihydroxylation 475 Woodward cw dihydroxylation 476 Prins reaction 478 Pschorr cyclization 480 Pummerer rearrangement 483 Ramberg Backlund reaction 485 Reformatsky reaction 487 Regitz diazo synthesis 489 Reimer Tiemann reaction 492 Reissert aldehyde synthesis 494 Reissert indole synthesis 497 Ring closing metathesis 499 Ritter reaction 501 Robinson annulation 503 Robinson Gabriel synthesis 505 Robinson Schopf reaction 507 Rosenmund reduction 509 Rubottom oxidation 511 Rupe rearrangement 513 Saegusa oxidation 515 Sakurai allylation reaction 518 Sandmeyer reaction 520 Schiemann reaction 522 Schmidt reaction 524 Schmidt's trichloroacetimidate glycosidation reaction 526 Shapiro reaction 529 Sharpless asymmetric amino hydroxylation 531 Sharpless asymmetric epoxidation 533 Sharpless asymmetric dihydroxylation 536 Sharpless olefin synthesis 540 Simmons Smith reaction 543 Skraup quinoline synthesis 545 Doebner von Miller reaction 547 Smiles rearrangement 549 Newman Kwart reaction 551 Truce Smile rearrangement 553 Sommelet reaction 555 Sommelet Hauser rearrangement 557 Sonogashira reaction 559 Staudinger ketene cycloaddition 561 Staudinger reduction 563 XVII Stembach benzodiazepine synthesis 565 Stetter reaction 567 Still Gennari phosphonate reaction 569 Stille coupling 571 Stille Kelly reaction 573 Stobbe condensation 575 Stork enamine reaction 577 Strecker amino acid synthesis 579 Suzuki coupling 581 Swern oxidation 583 Takai iodoalkene synthesis 585 Tebbe olefmation 587 Petasis alkenylation 587 TEMPO mediated oxidation 589 Thorpe Ziegler reaction 592 Tsuji Trost allylation 594 Ugi reaction 596 Ullmann reaction 599 van Leusen oxazole synthesis 601 Vilsmeier Haack reaction 603 Vilsmeier mechanism for acid chloride formation 605 Vinylcyclopropane cyclopentene rearrangement 606 von Braun reaction 608 Wacker oxidation 610 Wagner Meerwein rearrangement 612 Weiss Cook reaction 614 Wharton oxygen transposition reaction 616 Willgerodt Kindler reaction 618 Wittig reaction 621 Schlosser modification of the Wittig reaction 622 [1,2] Wittig rearrangement 624 [2,3] Wittig rearrangement 626 Wohl Ziegler reaction 628 Wolff rearrangement 630 Wolff Kishner reduction 632 Yamaguchi esterification 634 Zincke reaction 637 Subject Index 641
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author	Li, Jie Jack 1964-
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edition	3., expanded ed.
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genre	(DE-588)4066724-8 Wörterbuch gnd-content
genre_facet	Wörterbuch
id	DE-604.BV021685207
illustrated	Illustrated
index_date	2024-07-02T15:12:42Z
indexdate	2024-11-25T17:26:05Z
institution	BVB
isbn	9783540300304 3540300309
language	English
oai_aleph_id	oai:aleph.bib-bvb.de:BVB01-014899365
oclc_num	69733151
open_access_boolean
owner	DE-703 DE-91G DE-BY-TUM DE-29T DE-19 DE-BY-UBM DE-M49 DE-BY-TUM DE-20 DE-634 DE-11
owner_facet	DE-703 DE-91G DE-BY-TUM DE-29T DE-19 DE-BY-UBM DE-M49 DE-BY-TUM DE-20 DE-634 DE-11
physical	XX, 652 S. Ill., graph. Darst. 235 mm x 155 mm
publishDate	2006
publishDateSearch	2006
publishDateSort	2006
publisher	Springer
record_format	marc
spellingShingle	Li, Jie Jack 1964- Name reactions a collection of detailed reaction mechanisms Composés organiques - Synthèse ram Réactions chimiques organiques - Mécanismes ram Chemical reactions Chemistry, Organic Reaktionsmechanismus (DE-588)4177123-0 gnd Namensreaktion (DE-588)4171139-7 gnd Organische Chemie (DE-588)4043793-0 gnd
subject_GND	(DE-588)4177123-0 (DE-588)4171139-7 (DE-588)4043793-0 (DE-588)4066724-8
title	Name reactions a collection of detailed reaction mechanisms
title_auth	Name reactions a collection of detailed reaction mechanisms
title_exact_search	Name reactions a collection of detailed reaction mechanisms
title_exact_search_txtP	Name reactions a collection of detailed reaction mechanisms
title_full	Name reactions a collection of detailed reaction mechanisms Jie Jack Li
title_fullStr	Name reactions a collection of detailed reaction mechanisms Jie Jack Li
title_full_unstemmed	Name reactions a collection of detailed reaction mechanisms Jie Jack Li
title_short	Name reactions
title_sort	name reactions a collection of detailed reaction mechanisms
title_sub	a collection of detailed reaction mechanisms
topic	Composés organiques - Synthèse ram Réactions chimiques organiques - Mécanismes ram Chemical reactions Chemistry, Organic Reaktionsmechanismus (DE-588)4177123-0 gnd Namensreaktion (DE-588)4171139-7 gnd Organische Chemie (DE-588)4043793-0 gnd
topic_facet	Composés organiques - Synthèse Réactions chimiques organiques - Mécanismes Chemical reactions Chemistry, Organic Reaktionsmechanismus Namensreaktion Organische Chemie Wörterbuch
url	http://deposit.dnb.de/cgi-bin/dokserv?id=2838724&prov=M&dok_var=1&dok_ext=htm http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=014899365&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA
work_keys_str_mv	AT lijiejack namereactionsacollectionofdetailedreactionmechanisms

Name reactions a collection of detailed reaction mechanisms

MARC

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