Handbook of synthetic photochemistry:
Gespeichert in:
| Weitere Verfasser: | |
|---|---|
| Format: | Buch |
| Sprache: | English |
| Veröffentlicht: |
Weinheim
Wiley-VCH
2010
|
| Schlagworte: | |
| Online-Zugang: | Inhaltstext Inhaltsverzeichnis |
| Beschreibung: | Literaturangaben |
| Beschreibung: | XIX, 463 S. Ill., graph. Darst. |
| ISBN: | 9783527323913 |
Internformat
MARC
| LEADER | 00000nam a2200000 c 4500 | ||
|---|---|---|---|
| 001 | BV025595296 | ||
| 003 | DE-604 | ||
| 005 | 20110504 | ||
| 007 | t | ||
| 008 | 100417s2010 ad|| |||| 00||| eng d | ||
| 015 | |a 10,A03 |2 dnb | ||
| 016 | 7 | |a 994010761 |2 DE-101 | |
| 020 | |a 9783527323913 |9 978-3-527-32391-3 | ||
| 035 | |a (OCoLC)501314758 | ||
| 035 | |a (DE-599)BVBBV025595296 | ||
| 040 | |a DE-604 |b ger |e rakwb | ||
| 041 | 0 | |a eng | |
| 049 | |a DE-11 |a DE-19 |a DE-384 | ||
| 082 | 0 | |a 547.135 |2 22/ger | |
| 084 | |a VK 5600 |0 (DE-625)147407:253 |2 rvk | ||
| 084 | |a 540 |2 sdnb | ||
| 245 | 1 | 0 | |a Handbook of synthetic photochemistry |c ed. by Angelo Albini ... |
| 264 | 1 | |a Weinheim |b Wiley-VCH |c 2010 | |
| 300 | |a XIX, 463 S. |b Ill., graph. Darst. | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b n |2 rdamedia | ||
| 338 | |b nc |2 rdacarrier | ||
| 500 | |a Literaturangaben | ||
| 650 | 0 | 7 | |a Organische Synthese |0 (DE-588)4075695-6 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Fotochemie |0 (DE-588)4045873-8 |2 gnd |9 rswk-swf |
| 689 | 0 | 0 | |a Fotochemie |0 (DE-588)4045873-8 |D s |
| 689 | 0 | 1 | |a Organische Synthese |0 (DE-588)4075695-6 |D s |
| 689 | 0 | |5 DE-604 | |
| 700 | 1 | |a Albini, Angelo |d 1946- |0 (DE-588)140159193 |4 edt | |
| 856 | 4 | 2 | |q text/html |u http://deposit.dnb.de/cgi-bin/dokserv?id=3294483&prov=M&dok_var=1&dok_ext=htm |3 Inhaltstext |
| 856 | 4 | 2 | |m DNB Datenaustausch |q application/pdf |u http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=020191332&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |3 Inhaltsverzeichnis |
| 943 | 1 | |a oai:aleph.bib-bvb.de:BVB01-020191332 | |
Datensatz im Suchindex
| _version_ | 1805093893011668992 |
|---|---|
| adam_text |
IMAGE 1
VII
CONTENTS
FOREWORD V PREFACE XV
LIST OF CONTRIBUTORS XVII
1 PHOTOCHEMICAL METHODS 1
ANGELO ALBINI AND LUCA GERMANI 1.1 PHOTOCHEMICAL METHODS 3
1.1.1 PHOTOCHEMISTRY AND ORGANIC SYNTHESIS 1 1.2 IRRADIATION APPARATUS 2
1.2.1 GENERAL 2
1.2.2 LOW-PRESSURE MERCURY ARCS 3 1.2.3 MEDIUM- AND HIGH-PRESSURE
MERCURY ARCS 7 1.2.4 OTHER LIGHT SOURCES 9
1.3 FURTHER EXPERIMENTAL PARAMETERS 11 1.3.1 CONCENTRATION AND SCALE 11
1.3.2 EFFECT OF IMPURITIES, OXYGEN, AND TEMPERATURE 15 1.3.3 SAFETY 17
1.3.4 PLANNING A PHOTOCHEMICAL SYNTHESIS 17 1.4 PHOTOCHEMICAL STEPS IN
SYNTHETIC PLANNING 19 REFERENCES 22
2 CARBON-CARBON BOND FORMATION BY THE PHOTOELIMINATION OF SMALL
MOLECULES IN SOLUTION AND IN CRYSTALS 25 SAORI SHIRAKI AND MIGUEL A.
GARCIA-GANBAY 2.1 INTRODUCTION 25
2.1.1 SYNTHESIS OF UNSTABLE MOLECULES 27 2.2 PHOTOCHEMICAL *-C BOND
FORMATION IN SOLUTION 30 2.2.1 CONCERTED REACTIONS 30 2.2.2
PHOTOELIMINATION OF N 2 31
2.2.2.1 SYNTHESIS OF THREE-MEMBERED RINGS 31
BIBLIOGRAFISCHE INFORMATIONEN HTTP://D-NB.INFO/994010761
DIGITALISIERT DURCH
IMAGE 2
VILI CONTENTS
2.2.2.2 SYNTHESIS OF CYCLOBUTANES AND POLYCYDIC COMPOUNDS 33
2.2.3 PHOTOELIMINATION OF CO FROM KETONES IN SOLUTION 35 2.2.4
PHOTOELIMINATION OF CO 2 FROM LACTONES 39 2.2.5 PHOTOELIMINATION OF
SULFUR FROM SULFIDES, SULFOXIDES, AND SULFONES 40
2.3 REACTIONS IN THE SOLID STATE 41
2.3.1 REACTIVITY AND STABILITY IN THE SOLID STATE 42 2.3.2 RESTRICTING
THE FATE OF THE RADICAL INTERMEDIATES IN SOLIDS 43 2.3.3 CRYSTALLINE
DIACYL PEROXIDES 44 2.3.4 DECARBONYLATION OF CRYSTALLINE KETONES 50
2.3.4.1 EARLY OBSERVATIONS 50 2.3.4.2 REACTIVITY AND STABILITY 51
2.3.4.3 THE RSE 11 KCAL * * * 1 CONDITION 53 2.3.4.4 SCOPE OF THE
REACTION 55 2.3.4.5 REACTION ENANTIOSPECIFICITY 56 2.3.4.6 SYNTHESIS OF
NATURAL PRODUCTS 57
2.3.4.7 QUENCHING EFFECTS 57 2.3.4.8 REACTION SCALE AND EXPERIMENTAL
CONDITIONS 59 2.4 CONCLUDING REMARKS 60
REFERENCES 60
3 INTERMOLECULAR ADDITION REACTIONS ONTO *-C MULTIPLE BONDS 67 VALENTINA
DICHIARANTE AND MAURIZIO FAGNONI 3.1 INTRODUCTION 67
3.1.1 SCOPE AND MECHANISM 68 3.2 ADDITION TO *-C DOUBLE BONDS 69
3.2.1 H-* ADDITION (HYDROALKYLATION REACTIONS) 69 3.2.1.1 ADDITION OF
ALKANES 70 3.2.1.2 ADDITION OF ALCOHOLS (HYDROHYDROXYMETHYLATION),
ETHERS, AND (2-SUBSTITUTED) 1,3-DIOXOLANE(S) 71
3.2.1.3 ADDITION OF AMINES (HYDROAMINOMETHYLATION) OR AMIDES 72 3.2.1.4
HYDROFLUOROMETHYLATION 74 3.2.1.5 ADDITION OF NITRITES OR KETONES 75
3.2.1.6 HYDROACYLATION AND HYDROCARBOXYLATION REACTIONS 75 3.2.1.7
HYDROARYLATION (PHOTO-EOCAS) 76 3.2.2 *-N ADDITION (HYDROAMINATION) 76
3.2.3 *-P ADDITION 78
3.2.4 H-* ADDITION 80
3.2.5 H-S ADDITION 82
3.2.6 ADDITION OFX-Y REAGENTS TO ALKENES 83 3.2.6.1 HALOGENATION 84
3.2.6.2 ADDITION WITH THE FORMATION OF *-C BONDS 84 3.3 ADDITION TO *-C
TRIPLE BONDS 86
3.3.1 HYDROALKYLATION REACTIONS 87 3.3.2 ADDITION OF X-Y REAGENTS 87
IMAGE 3
CONTENTS IX
3.4 CONCLUDING REMARKS 88
REFERENCES 89
4 FORMATION OF A THREE-MEMBERED RING 95 TAKASHI TSUNO 4.1 INTRODUCTION
95
4.2 DI-7T-METHANE REARRANGEMENT 96 4.2.1 DI-JI-METHANE REARRANGEMENT OF
BARRELENE, BENZOBARRELENE, DIBENZOBARRELENE, AND RELATED DERIVATIVES 96
4.2.2 DI-*-****** REARRANGEMENT OF ACYCLIC SYSTEMS 100 4.2.3
DI-JT-METHANE REARRANGEMENT IN NATURAL COMPOUNDS 103 4.3
OXA-DI-TI-METHANE REARRANGEMENT AND RELATED
REARRANGEMENTS 105 4.3.1 OXA-DI-TT-METHANE REARRANGEMENT OF
SS.Y-UNSATURATED KETONES AND ALDEHYDES 105 4.3.2 AZA-DI-7T-METHANE
REARRANGEMENT 109 4.3.3 SYNTHETIC APPLICATIONS OF OXA-DI-7T-METHANE
REARRANGEMENT 110 4.4 [2+1] CYCLOADDITION OF ALKENES WITH CARBENES 111
4.4.1 INTRAMOLECULAR [2+1] CYCLOADDITION 111 4.4.2 NOVEL TRIPLET
SENSITIZERS FOR THE GENERATION OF CARBENES 111 4.4.3 METAL-CATALYZED
CYCLOPROPANATION-SUPPORTED PHOTOCHEMISTRY 112 4.4.4 NOVEL PRECURSORS OF
CARBENES 113 4.5 FORMATION OF A CYCLOPROPANE VIA INTRAMOLECULAR HYDROGEN
ABSTRACTION 114
4.5.1 FORMATION OF CYDOPROPANOL VIA INTRAMOLECULAR SS-HYDROGEN
ABSTRACTION 115 4.5.2 FORMATION OF CYCLOPROPANE RING VIA INTRAMOLECULAR
Y-HYDROGEN ABSTRACTION 117
4.6 [3+2] CYCLOADDITION OF ARENES WITH ALKENES 119 4.6.1 INTERMOLECULAR
[3+2] CYCLOADDITION 119 4.6.2 INTRAMOLECULAR [3+2] CYCLOADDITION 119
4.6.3 APPLICATION OF THE PHOTOCHEMICAL [3+2] CYCLOADDITION IN THE
SYNTHESIS OF NATURAL PRODUCTS 122 4.7 PHOTOCHEMICAL SYNTHESIS OF
THREE-MEMBERED HETEROCYCLES 123 4.7.1 EPOXIDES 123
4.7.2 AZIRIDINES 123
REFERENCES 126
5 FORMATION OF A FOUR-MEMBERED RING 137 NORBERT HOFFMANN 5.1
INTRODUCTION 137
5.2 [2+2]-PHOTOCYDOADDITION OF NONCONJUGATED ALKENES 137 5.3
[2+2]-PHOTOCYDOADDITION OF AROMATIC COMPOUNDS 144 5.4 PHOTOCHEMICAL
ELECTROCYCLIC REACTIONS 150 5.5 INTRAMOLECULAR Y-HYDROGEN ABSTRACTION
(YANG REACTION) 153
IMAGE 4
X CONTENTS
5.6 METAL-CATALYZED REACTIONS 156
5.7 OTHER METHODS 157
5.8 CONDUDING REMARKS 160
REFERENCES 160
6 FORMATION OF A FOUR-MEMBERED RING: FROM A CONJUGATE ALKENE 171 JOERG P.
HEHN, CHRISTIANE MUELLER, AND THORSTEN BACH
6.1 INTRODUCTION 171
6.2 [2+2]-PHOTOCYDOADDITION OF ENONES (SUBSTRATE TYPE AL) 173 6.2.1
CYCLOPENTENONES 173 6.2.2 CYDOHEXENONES 177 6.2.3 PARO-QUINONES AND
RELATED SUBSTRATES 181
6.3 [2+2]-PHOTOCYDOADDITION OF VINYLOGOUS AMIDES AND ESTERS (SUBSTRATE
CLASSES A2 AND A3) 182 6.3.1 ENDOCYDIC HETEROATOM Q IN SS-POSITION
(SUBSTRATE CLASS A2) 183 6.3.1.1 4-HETERO-2-CYDOPENTENONES 183
6.3.1.2 4-HETERO-2-CYDOHEXENONES 185 6.3.2 EXOCYCLIC HETEROATOM Q IN
SS-POSITION (SUBSTRATE CLASS A3) 186 6.4 [2+2]-PHOTOCYCLOADDITON OF A,
SS-UNSATURATED CARBOXYLIC ADD DERIVATIVES (SUBSTRATE CLASSES A4, A5, AND
A6) 389
6.4.1 NO FURTHER HETEROATOM Q IN SS-POSITION (SUBSTRATE CLASS A4) 189
6.4.1.1 OT,SS-UNSATURATED LACTONES 189 6.4.1.2 A,SS-UNSATURATED LACTAMS
192 6.4.1.3 COUMARINS 193 6.4.1.4 QUINOLONES 194
6.4.1.5 MALEIC ANHYDRIDE AND DERIVATIVES 196 6.4.1.6 SULFUR COMPOUNDS
197 6.4.2 ENDOCYDIC HETEROATOM Q IN SS-POSITION (SUBSTRATE CLASS A5) 198
6.4.2.1 L,3-DIOXIN-4-ONES 198 6.4.2.2 4-PYRIMIDINONES 200 6.4.3
EXOCYCLIC HETEROATOM Q IN SS-POSITION (SUBSTRATE CLASS A6) 201 6.4.3.1
LACTONES 202 6.4.3.2 LACTAMS 203 6.5 CONDUDING REMARKS 205
REFERENCES 205
7 FORMATION OF A FOUR-MEMBERED RING: OXETANES 217 MANABU ABE 7.1
INTRODUCTION 217
7.2 THE GENERALLY ACCEPTED MECHANISM OF THE PATERNO-BUECHI REACTION 220
7.3 REGIOSELECTIVE AND SITE-SELECTIVE SYNTHESES OF OXETANES 221 7.4
STEREOSELECTIVE SYNTHESES OF OXETANES 226 7.5 CONCLUDING REMARKS 233
REFERENCES 233
IMAGE 5
CONTENTS XI
8 FORMATION OF A FIVE-MEMBERED RING 241
GANESH PANDEY AND SMITA R. GADRE 8.1 INTRODUCTION 241
8.2 FORMATION OF FIVE-MEMBERED RINGS: INTRAMOLECULAR 5-H ABSTRACTION 241
8.2.1 FORMATION OF CYCLOPENTANOL RING SYSTEM 242 8.2.1.1 SYNTHESIS OF
INDANOLS 243 8.2.2 SYNTHESIS OF TETRAHYDROFURANOLS 247 8.2.2.1 FORMATION
OF BENZOFURANOLS 250 8.2.3 SYNTHESIS OF PYRROLIDINE DERIVATIVES 250 8.3
FORMATION OF FIVE-MEMBERED RINGS VIA [3+2]-CYDOADDITIONS 254 8.3.1
PHOTOFRAGMENTATION OF OXIRANES TO CARBONYL YLIDES: SYNTHESIS OF
TETRAHYDROFURANS 254 8.3.2 GENERATION OF AZOMETHINE YLIDES BY THE
PHOTOLYSIS OF AZIRIDINES: SYNTHESIS OF THE PYRROLIDINE FRAMEWORK 258
8.3.3 VINYL CYCLOPROPANE TO CYDOPENTENE REARRANGEMENT 260 8.4
PHOTODIEMICAL ELECTROCYDIZATION REACTIONS: SYNTHESIS OF FUSED,
FIVE-MEMBERED RING COMPOUNDS 261 8.5 PHOTOINDUCED ELECTRON
TRANSFER-MEDIATED CYCLIZATIONS: SYNTHESIS OF FIVE-MEMBERED CARBOCYDIC
AND HETEROCYDIC RING SYSTEMS 266 8.5.1 RADICAL CATION-MEDIATED
CARBON-CARBON BOND FORMATION 266 8.5.2 RADICAL ANION-MEDIATED
CYCLIZATIONS 272 8.5.3 INTRAMOLECULAR TRAPPING OF RADICAL CATIONS BY
NUCLEOPHILES 276
REFERENCES 279
9 FORMATION OF SIX-MEMBERED (AND LARGER) RINGS 287 JULIA PEREZ-PRIETO
AND MIGUEL ANGEL MIRANDA 9.1 INTRODUCTION 287
9.2 PHOTOELECTRON TRANSFER-INITIATED CYCLIZATIONS 287 9.2.1 PHTHALIMIDES
AS ELECTION ACCEPTORS 287 9.2.2 AROMATIC KETONES AS ELECTRON ACCEPTORS
293
9.2.3 CHLOROACETAMIDES AS ELECTRON ACCEPTORS 292 9.2.4
ELECTRON-DEFICIENT AROMATIC COMPOUNDS AS ELECTRON ACCEPTORS 293 9.3
PHOTOINDUCED ORC-ELECTROCYCLIZATION 295
9.3.1 STILBENE-LIKE PHOTOCYCLIZATION 295 9.3.2 VINYL-BIPHENYLS
PHOTOCYDIZATION 299 9.3.3 ANILIDES AND ENAMIDES PHOTOCYCLIZATION 299 9.4
PHOTOCYCLOADDITION REACTIONS 300 9.4.1 PHOTOCHEMICAL DIELS-ALDER
REACTION 301
9.4.2 PHOTOENOLIZATION/DIELS-ALDER REACTION 302 9.4.3
[4+4]-PHOTOCYCLOADDITION 302 9.4.4 TRANSITION METAL TEMPLATE-CONTROLLED
REACTIONS 304 9.5 REMOTE INTRAMOLECULAR HYDROGEN ABSTRACTION 307 9.6
RING CONTRACTION AND RING ENLARGEMENT 308 9.7 OTHER REACTIONS 311
IMAGE 6
XII CONTENTS
9.7.1 INTRAMOLECULAR [2+2]-CYDOADDITIONS 311
9.7.2 PHOTOCYCLIZATION OF CINNAMYLANILIDES 33I 9.7.3 PHOTOCYDOADDITION
OF AROMATIC COMPOUNDS 311 9.8 CONDUDING REMARKS 313
REFERENCES 333
10 AROMATIC AND HETEROAROMATIC SUBSTITUTION BY S RN1 AND SN1 REACTIONS
339 ALICIA B. PENENORY AND JUAN E. ARGUELLO 10.1 INTRODUCTION 339
10.2 GENERAL MECHANISTIC FEATURES 320 10.2.1 S RN 1 MECHANISM 320
10.2.2 S N 1 MECHANISM 322 10.3 CARBON-CARBON BOND FORMATION 323 10.3.1
CARBANIONS FROM KETONES, ESTERS, ACIDS, AMIDES, AND IMIDES AS THE
NUDEOPHILES 323
10.3.2 ALKENES, ALKYNES, ENOLS, AND VINYL AMINES AS THE NUDEOPHILES 326
10.3.3 ARYL ALKOXIDE AND ARYL AMIDE ANIONS AS THE NUDEOPHILES 329 10.3.4
CYANIDE IONS AS THE NUDEOPHILE 333 10.4 CARBON-HETEROATOM BOND FORMATION
332
10.4.1 TIN NUDEOPHILES 332 10.4.2 SULFUR NUDEOPHILES 333 10.5 SYNTHESIS
OF BI-, TRI-, AND POLYARYLS 334 10.5.1 CONSECUTIVE S RN
L-PD(O)-CATALYZED CROSSCOUPLING REACTIONS 334
10.5.2 PHOTO-S N 1 AS AN ALTERNATIVE TO METAL CATALYSIS 336 10.6
SYNTHESIS OF CARBOCYDES AND HETEROCYDES 338 10.6.1 CARBOCYDES 338 10.6.2
NITROGEN HETEROCYDES 341
10.6.3 OXYGEN HETEROCYDES 344 10.6.4 SULFUR HETEROCYDES 346 REFERENCES
346
1I SINGLET OXYGEN AS A REAGENT IN ORGANIC SYNTHESIS 353 MATIBUR ZAMADAR
AND ALEXANDER CREER 11.1 INTRODUCTION 353
11.2 DIOXETANES 354
11.2.1 BACKGROUND INFORMATION 354 11.2.2 ADAMANTYL-SUBSTITUTED ALKENES
355 11.2.3 ALKOXY-SUBSTITUTED ALKENES 356 11.2.4 PHENYL-OR
METHYL-SUBSTITUTED ALKENES 357
11.2.4.1 DIPHENYLINDENE PHOTOOXIDARION 357 11.2.4.2 ELECTRON-TRANSFER
PHOTOOXIDATION 357 11.2.5 SUMMARY 358
11.3 ENDOPEROXIDES 358
11.3.1 BACKGROUND INFORMATION 358
IMAGE 7
CONTENTS XIII
11.3.2 ARENES 359
11.3.2.1 BENZENES 359 11.3.2.2 NAPHTHALENES 363 11.3.2.3 ANTHRACENES,
POLYACENES, AND CARBON NANOTUBES 362
11.3.3 ELECTRON-TRANSFER PHOTOOXIDATION 364 11.3.4 CONJUGATED DIENES 364
11.3.4.1 ACYCLIC DIENES 364 11.3.4.2 CYCLOPENTADIENES AND
CYCLOHEXADIENES 364 11.3.4.3 HETEROCYDES AND CYCLOHEXATRIENE 365
11.3.5 SUMMARY 368
11.4 ALLYLIC HYDROPEROXIDES 368 11.4.1 BACKGROUND INFORMATION 368 11.4.2
SIMPLE ALKENES 368 11.4.3 "ENE" REACTIONS CONFINED IN ZEOLITES 370
11.4.4 SUMMARY 370
11.5 TANDEM SINGLET OXYGEN REACTIONS 371 11.5.1 BACKGROUND INFORMATION
371 11.5.2 BISPEROXIDES 371 11.5.2.1 PHENYL-SUBSTITUTED ALKENES 371
11.5.2.2 CYDIC ALKENES 372
11.5.3 REARRANGEMENT TO A HEMIKETAL HYDROPEROXIDE 374 11.5.4
REARRANGEMENTS TO SPIRO COMPOUNDS 374 11.5.5 SUMMARY 376
11.6 CONDUDING REMARKS 377
REFERENCES 377
12 SYNTHESIS OF HETEROAROMATICS VIA REARRANGEMENT REACTIONS 387 NICOLO
VIVONO, SILVESTRE BUSCEMI, VANA PIBIRI, ANTONIO PALUMBO PICCIONELLO,
AND ANDREA PACE 12.1 INTRODUCTION 387
12.2 SYNTHESIS OF FIVE-MEMBERED RINGS WITH ONE HETEROATOM 388 12.2.1
PYRROLES 388
12.2.2 FURANS 391
12.2.3 THIOPHENES 392 12.3 SYNTHESIS OF FIVE-MEMBERED RINGS WITH TWO
HETEROATOMS 393 12.3.1 PYRAZOLES 393 12.3.2 IMIDAZOLES 394
12.3.3 OXAZOLES 398 12.3.4 THIAZOLES 400
12.4 SYNTHESIS OF FIVE-MEMBERED RINGS WITH THREE HETEROATOMS 402 12.4.1
OXADIAZOLES 402 12.4.2 TRIAZOLES 404
12.4.3 THIADIAZOLES 405 12.5 SYNTHESIS OF SIX-MEMBERED RINGS 406 12.6
SYNTHESIS OF SEVEN-MEMBERED RINGS 406
IMAGE 8
XIV CONTENTS
12.6.1
12.6.2 12.6.3 12.7
AZEPINES DIAZEPINES OXAZEPINES CONDUDING
REFERENCES
406 407 409 REMARKS 430
433
13 PHOTOLABILE PROTECTING CROUPS IN ORGANIC SYNTHESIS 437 CHRISTIAN G.
BOCHET AND AURELIEN BLANC 13.1 INTRODUCTION 417
13.2 PHOTOLABILE PROTECTING GROUPS 438 13.2.1 ORTHO-NITROBENZYL ALCOHOL
DERIVATIVES 438 13.2.2 BENZYL ALCOHOL DERIVATIVES 421 13.2.3 OTHER TYPES
OF PROTECTING GROUP 423
13.2.3.1 NORRISH TYPE II 423 13.2.3.2 NORRISH TYPE I 424 13.2.3.3
THIOKETALS 424 13.2.3.4 SILICON ETHERS 424
13.2.4 Z/E PHOTOISOMERIZATION 425 13.2.4.1 CINNAMYL ESTERS 425 13.2.5
PHENACYL DERIVATIVES 426 13.2.5.1 MECHANISM 426 13.2.6 BENZOIN
DERIVATIVES 428 13.2.6.1 MECHANISM 428
13.2.7 INDOLINES 429
13.3 CHROMATIC ORTHOGONALITY 430 13.4 TWO-PHOTONS ABSORPTION 431 13.5
CONDUDING REMARKS 432
13.6 APPENDIX 433
REFERENCES 439
INDEX 449 |
| any_adam_object | 1 |
| author2 | Albini, Angelo 1946- |
| author2_role | edt |
| author2_variant | a a aa |
| author_GND | (DE-588)140159193 |
| author_facet | Albini, Angelo 1946- |
| building | Verbundindex |
| bvnumber | BV025595296 |
| classification_rvk | VK 5600 |
| ctrlnum | (OCoLC)501314758 (DE-599)BVBBV025595296 |
| dewey-full | 547.135 |
| dewey-hundreds | 500 - Natural sciences and mathematics |
| dewey-ones | 547 - Organic chemistry |
| dewey-raw | 547.135 |
| dewey-search | 547.135 |
| dewey-sort | 3547.135 |
| dewey-tens | 540 - Chemistry and allied sciences |
| discipline | Chemie / Pharmazie |
| format | Book |
| fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>00000nam a2200000 c 4500</leader><controlfield tag="001">BV025595296</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">20110504</controlfield><controlfield tag="007">t</controlfield><controlfield tag="008">100417s2010 ad|| |||| 00||| eng d</controlfield><datafield tag="015" ind1=" " ind2=" "><subfield code="a">10,A03</subfield><subfield code="2">dnb</subfield></datafield><datafield tag="016" ind1="7" ind2=" "><subfield code="a">994010761</subfield><subfield code="2">DE-101</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9783527323913</subfield><subfield code="9">978-3-527-32391-3</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)501314758</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV025595296</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-11</subfield><subfield code="a">DE-19</subfield><subfield code="a">DE-384</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">547.135</subfield><subfield code="2">22/ger</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">VK 5600</subfield><subfield code="0">(DE-625)147407:253</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">540</subfield><subfield code="2">sdnb</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Handbook of synthetic photochemistry</subfield><subfield code="c">ed. by Angelo Albini ...</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Weinheim</subfield><subfield code="b">Wiley-VCH</subfield><subfield code="c">2010</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">XIX, 463 S.</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="500" ind1=" " ind2=" "><subfield code="a">Literaturangaben</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Organische Synthese</subfield><subfield code="0">(DE-588)4075695-6</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Fotochemie</subfield><subfield code="0">(DE-588)4045873-8</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="689" ind1="0" ind2="0"><subfield code="a">Fotochemie</subfield><subfield code="0">(DE-588)4045873-8</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="1"><subfield code="a">Organische Synthese</subfield><subfield code="0">(DE-588)4075695-6</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2=" "><subfield code="5">DE-604</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Albini, Angelo</subfield><subfield code="d">1946-</subfield><subfield code="0">(DE-588)140159193</subfield><subfield code="4">edt</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="q">text/html</subfield><subfield code="u">http://deposit.dnb.de/cgi-bin/dokserv?id=3294483&prov=M&dok_var=1&dok_ext=htm</subfield><subfield code="3">Inhaltstext</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="m">DNB Datenaustausch</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=020191332&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA</subfield><subfield code="3">Inhaltsverzeichnis</subfield></datafield><datafield tag="943" ind1="1" ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-020191332</subfield></datafield></record></collection> |
| id | DE-604.BV025595296 |
| illustrated | Illustrated |
| indexdate | 2024-07-20T10:34:43Z |
| institution | BVB |
| isbn | 9783527323913 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-020191332 |
| oclc_num | 501314758 |
| open_access_boolean | |
| owner | DE-11 DE-19 DE-BY-UBM DE-384 |
| owner_facet | DE-11 DE-19 DE-BY-UBM DE-384 |
| physical | XIX, 463 S. Ill., graph. Darst. |
| publishDate | 2010 |
| publishDateSearch | 2010 |
| publishDateSort | 2010 |
| publisher | Wiley-VCH |
| record_format | marc |
| spelling | Handbook of synthetic photochemistry ed. by Angelo Albini ... Weinheim Wiley-VCH 2010 XIX, 463 S. Ill., graph. Darst. txt rdacontent n rdamedia nc rdacarrier Literaturangaben Organische Synthese (DE-588)4075695-6 gnd rswk-swf Fotochemie (DE-588)4045873-8 gnd rswk-swf Fotochemie (DE-588)4045873-8 s Organische Synthese (DE-588)4075695-6 s DE-604 Albini, Angelo 1946- (DE-588)140159193 edt text/html http://deposit.dnb.de/cgi-bin/dokserv?id=3294483&prov=M&dok_var=1&dok_ext=htm Inhaltstext DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=020191332&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Handbook of synthetic photochemistry Organische Synthese (DE-588)4075695-6 gnd Fotochemie (DE-588)4045873-8 gnd |
| subject_GND | (DE-588)4075695-6 (DE-588)4045873-8 |
| title | Handbook of synthetic photochemistry |
| title_auth | Handbook of synthetic photochemistry |
| title_exact_search | Handbook of synthetic photochemistry |
| title_full | Handbook of synthetic photochemistry ed. by Angelo Albini ... |
| title_fullStr | Handbook of synthetic photochemistry ed. by Angelo Albini ... |
| title_full_unstemmed | Handbook of synthetic photochemistry ed. by Angelo Albini ... |
| title_short | Handbook of synthetic photochemistry |
| title_sort | handbook of synthetic photochemistry |
| topic | Organische Synthese (DE-588)4075695-6 gnd Fotochemie (DE-588)4045873-8 gnd |
| topic_facet | Organische Synthese Fotochemie |
| url | http://deposit.dnb.de/cgi-bin/dokserv?id=3294483&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=020191332&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
| work_keys_str_mv | AT albiniangelo handbookofsyntheticphotochemistry |