(3 + 3)-cyclodimerization of donor-acceptor cyclopropanes. three routes to six-membered rings

Journal of Organic Chemistry

Volumn 76, Issue 21, 2011, Pages 8852-8868

  Ivanova, Olga A ^a   Budynina, Ekaterina M ^a,b   Chagarovskiy, Alexey O ^b   Trushkov, Igor V ^a,b   Melnikov, Mikhail Ya ^a  

^a MOSCOW STATE UNIVERSITY   (Russian Federation)

^b Federal Research Center of Pediatric Hematology   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIC SYSTEMS; CYCLODIMERIZATION; DONOR-ACCEPTORS; LEWIS ACID; SIX-MEMBERED RINGS; SUBSTRATE PROPERTIES; TETRAHYDRONAPHTHALENES;

CARBOXYLATION;

PROPANE;

ANTHRACENE DERIVATIVE; DICARBOXYLIC ACID; DIETHYL 2 (3 BROMO 2,4,6 TRIMETHOXYPHENYL)CYCLOPROPANE 1,1 DICARBOXYLATE; DIMETHYL 2 (2,3 DIHYDROBENZO[B][1,4]DIOXIN 6 YL) CYCLOPROPANE 1,1 DICARBOXYLATE; DIMETHYL 2 (3,5 DIMETHOXYBENZYLIDENE)MALONATE; DIMETHYL 2 (3,5 DIMETHOXYPHENYL)CYCLOPROPANE 1,1DICARBOXYLATE; DIMETHYL 2 (4 PIPERIDINOBENZYLIDENE)MALONATE; DIMETHYL 2 (4 PIPERIDINOPHENYL)CYCLOPROPANE 1,1 DICARBOXYLATE; DIMETHYL 2 [(2,3 DIHYDROBENZO[B][1,4]DIOXIN 6 YL) METHYLENE]MALONATE; DIMETHYL 4 (3,4 DIMETHOXYPHENYL) 6,7 DIMETHOXY 1 (3 METHOXY 2 (METHOXYCARBONYL) 3 OXOPROPYL) 3,4 DIHYDRONAPHTALENE 2,2(1H) DICARBOXYLATE; DIMETHYL 5,6,7 TRIMETHOXY 1 [3 METHOXY 2 (METHOXYCARBONYL) 3 OXOPROPYL] 4 (3,4,5 TRIMETHOXYPHENYL) 3,4 DIHYDRONAPHTHALENE 2,2(1H) DICARBOXYLATE; DIMETHYL 6 METHOXY 1 (3 METHOXY 2 (METHOXYCARBONYL) 3 OXOPROPYL) 4 (4 METHOXYPHENYL) 3,4 DIHYDRONAPHTHALENE 2,2 (1H) DICARBOXYLATE; DIMETHYL 7 (3 METHOXY 2 (METHOXYCARBONYL) 3 OXOPROPYL) 2 METHYL 4 (5 METHYLTHIOPHENE 2 YL) 4,5 DIHYDROBENZO[B] THIOPHENE 6,6(7H) DICARBOXYLATE; DIMETHYL 7 (3 METHOXY 2 (METHOXYCARBONYL) 3 OXOPROPYL) 4 (THIOPHENE 2 YL) 4,5 DIHYDROBENZO[B]THIOPHENE 6,6(7H) DICARBOXYLATE; DIMETHYL 9 (2 DIHYDRO 1,4 BENZODIOXIN 6 YL) 6 [3' METHOXY 2' (METHOXYCARBONYL) 3' OXOPROPYL] 2,3,8,9 TETRAHYDRONAPHTHO[2,3 B][1,4]DIOXINE 7,7(6H) DICARBOXYLATE; LEWIS ACID; PROPANE; TETRAETHYL 3,6 BIS(2,4,6 TRIMETHOXYPHENYL)HEX 5 ENE 1,1,4,4 TETRACARBOXYLATE; TETRAETHYL 3,6 BIS(3 BROMO 2,4,6 TRIMETHOXYPHENYL) HEX 5 ENE 1,14,4 TETRACARBOXYLATE; TETRAETHYL CIS 2,5 BIS(2,4,6 TRIMETHOXYPHENYL)CYCLOHEXANE 1,1,4,4 TETRACARBOXYLATE; TETRAETHYL CIS 2,5 BIS(4 METHOXYPHENYL)CYCLOHEXANE 1,1,4,4 TETRACARBOXYLATE; TETRAETHYL CIS 2,5 BIS[4 (DIMETHYLAMINO)PHENYL] CYCLOHEXANE 1,1,4,4 TETRACARBOXYLATE; TETRAMETHYL 1 (4 METHOXYPHENYL) 7 OXO 3A,4,6,7 TETRAHYDRO 1H CYCLOPENTA[C]INDENE 3,3,5,5 (2H,5AH) TETRACRABOXYLATE; TETRAMETHYL 2,2' [(1,2,3,5,6,7 HEXAMETHOXY 9,10 DIHYDROANTHRACENE 9,10 DIYL)DI(METHYLENE]DIMALONATE; TETRAMETHYL 2,2' [(1,2,5,6 TETRAMETHOXY 9,10 DIHYDROANTHRACENE 9,10 DIYL)DI(METHYLENE)]MALONATE; TETRAMETHYL 2,2' [(1,3,5,7 TETRAMETHOXY 9,10 DIHYDROANTHRACENE 9, 10 DIYL)DI(METHYLENE)]DIMALONATE; TETRAMETHYL CIS 2,5 BIS(4 METHOXYPHENYL)CYCLOHEXANE 1,1,4,4 TETRACRBOXYLATE; TETRAMETHYL CIS 2,5 BIS(4 MORPHOLINOPHENYL)CYCLOHEXANE 1,1,4,4 TETRACARBOXYLATE; TETRAMETHYL CIS 2,5 BIS(4 PIPERIDINOPHENYL)CYCLOHEXANE 1,1,4,4 TETRACARBOXYLATE; TETRAMETHYL CIS 2,5 BIS[4 (DIMETHYLAMINO)PHENYL] CYCLOHEXANE 1,1,4,4 TETRACARBOXYLATE; UNCLASSIFIED DRUG;

ARTICLE; CRYSTAL STRUCTURE; DIMERIZATION; ELECTRON; PROTON NUCLEAR MAGNETIC RESONANCE; SUBSTITUTION REACTION; SYNTHESIS; X RAY ANALYSIS;

ANTHRACENES; CYCLIZATION; CYCLOHEXANES; CYCLOPROPANES; ELECTRONS; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 80055094769     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo201612w     Document Type: Article

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