D 3-trishomocubane-4-carboxylic acid as a new chiral building block: Synthesis and absolute configuration

Synthesis

Volumn 44, Issue 5, 2012, Pages 810-816

  Gaidai, Alexandr V ^a   Volochnyuk, Dmitriy M ^b   Shishkin, Oleg V ^c   Fokin, Andrey A ^a   Levandovskiy, Igor A ^a   Shubina, Tatyana E ^d  

^a NATIONAL TECHNICAL UNIVERSITY OF UKRAINE   (Ukraine)

^b INSTITUTE OF ORGANIC CHEMISTRY   (Ukraine)

^c INSTITUTE FOR SINGLE CRYSTALS   (Ukraine)

^d UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

absolute configuration; Corey Chaykovsky reaction; D 3 trishomocubane; stereochemistry

Indexed keywords

1 ,4-BENZOQUINONE; ABSOLUTE CONFIGURATION; CHIRAL BUILDING BLOCKS; COREY-CHAYKOVSKY REACTION; CYCLOPENTADIENES; EPOXIDE RING OPENING; OPTICALLY ACTIVE; PHENYLETHYLAMINES; X-RAY CRYSTAL STRUCTURE ANALYSIS;

BORON; ETHERS; OLEFINS; STEREOCHEMISTRY;

CARBOXYLIC ACIDS;

7 IODOPENTACYCLO[6.3.0 2,6 .0 3,10 .0 5,9]UNDECAN 4 OL; BORON TRIFLUORIDE; BORON TRIFLUORIDE DIETHYL ETHER; CARBOXYLIC ACID DERIVATIVE; ENDO TRICYCLO[6.2.1.0 2,7]UNDECA 4,9 DIENE 3,6 DIONE; EPOXIDE; METHYLPENTACYCLO[6.3.0 2,6 .0 3,10 .0 5,9]UNDECANE 4 CARBOXYLATE; PENTACYCLO[5.4.0.0 2,6 .0 3,10 .0 5,9]UNDECANE 8,11 DIOL; PENTACYCLO[5.4.0.0 2,6 .0 3,10 .0 5,9]UNDECANE 8,11 DIONE; PENTACYCLO[6.3.0 2,6 .0 3,10 .0 5,9]UNDECAN 4 OL; PENTACYCLO[6.3.0 2,6 .0 3,10 .0 5,9]UNDECAN 4 ONE; PENTACYCLO[6.3.0 2,6 .0 3,10 .0 5,9]UNDECAN 4 YL ACETATE; PENTACYCLO[6.3.0 2,6 .0 3,10 .0 5,9]UNDECANE 4 CARBALDEHYDE; PENTACYCLO[6.3.0 2,6 .0 3,10 .0 5,9]UNDECANE 4 CARBOXYLIC ACID; PENTACYCLO[6.3.0 2,6 .0 3,10 .0 5,9]UNDECANE 4 CARBOXYLIC ACID 1 PHENYLETHYLAMIDE; SPIRO[OXIRANE 2,4' PENTACYCLO[6.3.0 2,6 .0 3,10 .0 5,9]UNDECANE]; TRISHOMOCUBANE 4 CARBOXYLIC ACID; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CHEMICAL ANALYSIS; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; COREY CHAYKOVSKY REACTION; CRYSTAL STRUCTURE; CRYSTALLIZATION; DRUG STRUCTURE; DRUG SYNTHESIS; OXIDATION; RACEMIC MIXTURE; X RAY DIFFRACTION;

EID: 84857454879     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0031-1289708     Document Type: Article

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