Studies on cycloaddition of cyclohexa-2,4-dienones and transformation of adducts: A general, stereoselective route to multifunctional bicyclo[2.2.2]octanes and diquinanes

Synthesis

Volumn , Issue 17, 2008, Pages 2719-2728

  Singh, Vishwakarma ^a   Chandra, Girish ^a   Mobin, Shaikh M ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY BOMBAY   (India)

Author keywords

Diels Alder reaction; Pericyclic reaction; Photochemistry; Rearrangements

Indexed keywords

ETHERS; FUNCTIONAL GROUPS; ORGANIC COMPOUNDS;

BICYCLOOCTENONES; DIELS-ALDER REACTION; DIENONES; DIVERSE FUNCTIONALITIES; FUNCTIONALIZED; IN-SITU; PERICYCLIC REACTION; PHOTOCHEMISTRY; REARRANGEMENTS; REDUCTIVE CLEAVAGE; STEREO-SELECTIVE; TRIPLET-SENSITIZED IRRADIATION; VINYL ACETATE; VINYL ETHERS; VINYL SULFONES;

CHROMOPHORES;

1,5 DIMETHYL 7 ENDO (PHENYLSULFONYL)BICYCLO[2.2.2]OCT 5 EN 2 ONE; 1,8 DIMETHYL 7 EXO (PHENYLSULFONYL)TRICYCLO[3.3.0.0 2,8]OCTAN 3 ONE; 3 (CHLOROMETHYL) 3 HYDROXY 1,5 DIMETHYL 7 ENDO (PHENYLSULFONYL)BICYCLO[2.2.2]OCT 5 EN 2 ONE; 3 (CHLOROMETHYL) 3 HYDROXY 5,6 DIMETHYL 7 ENDO (PHENYLSULFONYL)BICYCLO[2.2.2]OCT 5 EN 2 ONE; 3 (CHLOROMETHYL) 3 HYDROXY 7 ENDO (PHENYLSULFONYL)BICYCLO[2.2.2]OCT 5 EN 2 ONE; 3 (CHLOROMETHYL) 7 ENDO ETHOXY 3 HYDROXY 1,5 DIMETHYLBICYCLO[2.2.2]OCT 5 EN 2 ONE; 3 (CHLOROMETHYL) 7 ENDO ETHOXY 3 HYDROXY 5,6 DIMETHYLBICYCLO[2.2.2]OCT 5 EN 2 ONE; 3 (CHLOROMETHYL) 7 ENDO ETHOXY 3 HYDROXYBICYCLO[2.2.2]OCT 5 EN 2 ONE; 3 (HYDROXYMETHYL) 1,5 DIMETHYL 7 ENDO (PHENYLSULFONYL)BICYCLO[2.2.2]OCT 5 EN 2 ONE; 4,6 DIMETHYL 8 ENDO (PHENYLSULFONYL)SPIRO[BICYCLO[2.2.2]OCT 5 ENE 2,2' OXIRAN] 3 ONE; 7 ENDO (PHENYLSULFONYL)BICYCLO[2.2.2]OCT 5 EN 2 ONE; 7 ENDO ACETOXY 3 (CHLOROMETHYL) 3 HYDROXY 5,6 DIMETHYLBICYCLO[2.2.2]OCT 5 EN 2 ONE; 7 ENDO ACETOXY 3 (CHLOROMETHYL) 3 HYDROXYBICYCLO[2.2.2]OCT 5 EN 2 ONE; 7 ENDO BUTOXY 3 (CHLOROMETHYL) 3 HYDROXY 1,5 DIMETHYLBICYCLO[2.2.2]OCT 5 EN 2 ONE; 7 ENDO BUTOXY 3 (CHLOROMETHYL) 3 HYDROXY 5,6 DIMETHYLBICYCLO[2.2.2]OCT 5 EN 2 ONE; 7 ENDO BUTOXY 3 (CHLOROMETHYL) 3 HYDROXYBICYCLO[2.2.2]OCT 5 EN 2 ONE; 7 ENDO BUTOXY 3 (HYDROXYMETHYL)BICYCLO[2.2.2]OCT 5 EN 2 ONE; 7 ENDO BUTOXYBICYCLO[2.2.2]OCT 5 EN 2 ONE; 7 EXO (PHENYLSULFONYL)TRICYCLO[3.3.0.0 2,8]OCTAN 3 ONE; 7 EXO ACETOXY 3 (CHLOROMETHYL) 3 HYDROXY 5,6 DIMETHYLBICYCLO[2.2.2]OCT 5 EN 2 ONE; 7 EXO ACETOXY 3 (CHLOROMETHYL) 3 HYDROXYBICYCLO[2.2.2]OCT 5 EN 2 ONE; 7 EXO ACETOXY 4 (CHLOROMETHYL) 4 HYDROXYTRICYCLO[3.3.0.0]OCTAN 3 ONE; 7 EXO BUTOXYTRICYCLO[3.3.0.0 2,8]OCTAN 3 ONE; 8 ENDO (PHENYLSULFONYL)SPIRO[BICYCLO[2.2.2]OCT 5 ENE 2,2' OXIRAN] 3 ONE; 8 ENDO BUTOXYSPIRO[BICYCLO[2.2.2]OCT 5 ENE 2,2' OXIRAN] 3 ONE; BICYCLO[2.2.2]OCTANE DERIVATIVE; CYCLOHEXANE DERIVATIVE; ETHYL 7 EXO BUTOXY 3 OXOBICYCLO[3.3.0]OCTANE 3 CARBOXYLATE; ETHYL 7 EXO BUTOXY 3 OXOTRICYCLO[3.3.0.0 2,8]OCTANE 4 CARBOXYLATE; UNCLASSIFIED DRUG; VINYL ACETATE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHROMATOPHORE; COLUMN CHROMATOGRAPHY; CYCLOADDITION; DIELS ALDER REACTION; OXIDATION; PHOTOCHEMISTRY; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; X RAY CRYSTALLOGRAPHY;

EID: 51949111329     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1067203     Document Type: Article

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