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| Smith M.B., March J. — March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure |
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| Предметный указатель |
[1,3]-Rearrangements alkyl sigmatropic, allyl vinyl ethers 1442
[1,3]-Rearrangements alkyl sigmatropic, and orbital symmetry 1441
[1,3]-Rearrangements alkyl sigmatropic, and stereochemistry 144^
[1,3]-Rearrangements alkyl sigmatropic, radical mechanism 1442
[1,3]-Rearrangements alkyl sigmatropic, thermal and photochemical 1441—1442
[1,3]-Rearrangements alkyl sigmatropic, vinylcyclopropane 1443
[1,3]-Rearrangements H sigmatropic, and the frontier orbital method 1438
[1,3]-Rearrangements H sigmatropic, and the Mobius — Hueckel method 1439
[1,5]-Homodienyl shifts and vinylcyclopropane rearrangement 1444
[1,5]-Homodienyl shifts hydrogen shift 1450
[1,5]-Homosigmatropic rearrangement 1450
[1,5]-Rearrangements alkyl sigmatropic 1440—1445
[1,5]-Rearrangements alkyl sigmatropic, and diradicals 1443
[1,5]-Rearrangements alkyl sigmatropic, and stereochemistry 1441
[1,5]-Rearrangements alkyl sigmatropic, thermal and photochemical 1441—1442
[1,5]-Rearrangements H sigmatropic 1437—1440
[1,5]-Rearrangements H sigmatropic, and the frontier orbital method 1438
[1,5]-Rearrangements H sigmatropic, and the Mobius — Hueckel method 1439
[1,5]-Rearrangements H sigmatropic, homodienyl 1440
[1,5]-Rearrangements H sigmatropic, orbital symmetry rules 1438
[1,5]-Rearrangements H sigmatropic, suprafacial and antarafacial 1437
[1,5]-Rearrangements H sigmatropic, with vinyl aziridines 1440
[1,5]-Rearrangements homosigmatropic 1450
[1,5]-Rearrangements sigmatropic 1436
[1,5]-Rearrangements sigmatropic, and semidine formation 1456
[1,7]-Rearrangements, sigmatropic, in radical cyclization 1440
[10]-Annulene, and aromaticity 62
[10]-Annulenes, derivatives and aromaticity 63
[18]-Annulene, structure 44
[2+2]-Cycloadditions 1077—1084
[2+2]-Cycloadditions a diion mechanism 1080
[2+2]-Cycloadditions and Diels — Alder reactions 1077
[2+2]-Cycloadditions and electrocyclic rearrangements 1434
[2+2]-Cycloadditions and orbital overlap 1079
[2+2]-Cycloadditions and the Wittig reaction 1235
[2+2]-Cycloadditions of cyclopentyne 1392
| [2+2]-Cycloadditions with allenes 1077
[2+2]-Cycloadditions with enamines 1077
[2+2]-Cycloadditions with ketenes 1077
[2+2]-Cycloadditions, alkenes with aldehydes or ketones 1249
[2+2]-Cycloadditions, catalysis 1083
[2+2]-Cycloadditions, diradical mechanism 1080
[2+2]-Cycloadditions, endo/exo isomers 1079
[2+2]-Cycloadditions, exciplex formation 1082
[2+2]-Cycloadditions, formation of  -lactams 1250
[2+2]-Cycloadditions, imines andketenes 1250
[2+2]-Cycloadditions, masochistic steric effects 1080
[2+2]-Cycloadditions, mechanism 1078
[2+2]-Cycloadditions, photochemical mechanism 1082
[2+2]-Cycloadditions, photochemical, intramolecular 1082
[2+2]-Cycloadditions, photochemical, orbital overlap 1069
[2+2]-Cycloadditions, retro 1081
[2+2]-Cycloadditions, the Paterno — Biichi reaction 1249
[2,2]-tetrabenzoparacyclophane, bond distances 19
[2,3]-Rearrangements, [2,3] Wittig 1454
[2,3]-Rearrangements, [2,3] Wittig sigmatropic 915 1453—1455
[2,3]-Rearrangements, [2,3] Wittig sigmatropic, enantioselectivity 1454
[2,3]-Rearrangements, [2,3] Wittig sigmatropic, Mislow — Evans 1455
[3+2]-Cycloadditions and ally lie anions 1076
[3+2]-Cycloadditions and diradicals 1076
[3+2]-Cycloadditions and enantioselectivity 1061
[3+2]-Cycloadditions and nonsynchronous mechanisms 1061
[3+2]-Cycloadditions, all carbon 1075
[3+2]-Cycloadditions, azides and alkenes 1059
[3+2]-Cycloadditions, common 1,3-dipolar compounds 1060
[3,3]-Rearrangements sigmatropic 1436
[3,3]-Rearrangements sigmatropic, Claisen rearrangement see “Claisen rearrangement”
[3,3]-Rearrangements sigmatropic, Cope see “Cope rearrangement”
[4+2]-Cycloadditions 1062—1075; see “Diels — Alder reactions”
[4+4+4]-, with dienes 1091
[4+4]-, with dienes 1091
[5,5]-Rearrangements sigmatropic, and benzidine rearrangements 1456
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