Chiral photochemistry within a confined space: Diastereoselective photorearrangements of a tropolone and a cyclohexadienone included in a synthetic cavitand

Dalton Transactions

Volumn , Issue 20, 2009, Pages 4003-4011

  Sundaresan, Arun Kumar ^a   Kaanumalle, Lakshmi S ^a   Gibb, Corinne L D ^b   Gibb, Bruce C ^b   Ramamurthy, V ^a  

^a Department of Biology   (United States)

^b UNIVERSITY OF NEW ORLEANS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETONITRILE SOLUTIONS; CAVITAND; CHIRAL AUXILIARIES; CHIRAL CENTERS; CHIRAL INDUCTION; CONFINED SPACE; DIASTEREOSELECTIVE; DIASTEREOSELECTIVITIES; ELECTROCYCLIZATION; GUEST-HOST; NMR STUDIES; PHOTOREACTIONS; PHOTOTRANSFORMATIONS; PROBE MOLECULES; REACTION CENTER; SUPRAMOLECULAR ASSEMBLIES; SUPRAMOLECULAR STRUCTURE; TRIPLET STATE; TROPOLONE;

ACETONITRILE; CYCLOHEXANE; METHANE; PROBES; SPACE PROBES; SUPRAMOLECULAR CHEMISTRY;

PHOTOCHEMICAL REACTIONS;

CAVITAND; CYCLOHEXADIENONE; CYCLOHEXENE DERIVATIVE; ETHER DERIVATIVE; RESORCINOL DERIVATIVE; TROPOLONE;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PHOTOCHEMISTRY; STEREOISOMERISM;

CYCLOHEXENES; ETHERS, CYCLIC; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; PHOTOCHEMISTRY; RESORCINOLS; STEREOISOMERISM; TROPOLONE;

EID: 65649149692     PISSN: 14779226     EISSN: 14779234     Source Type: Journal    
DOI: 10.1039/b900017h     Document Type: Article

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