The [2+2]-photocycloaddition of aromatic aldehydes and ketones to 3,4-dihydro-2-pyridones: Regioselectivity, diastereoselectivity, and reductive ring opening of the product oxetanes

Chemistry - A European Journal

Volumn 7, Issue 20, 2001, Pages 4512-4521

  Bach, Thorsten ^a,b   Bergmann, Hermann ^a   Brummerhop, Harm ^a   Lewis, Warren ^a   Harms, Klaus ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

^b TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

Asymmetric synthesis; Cycloaddition; Hydrogen bonds; Patern B chi reactions; Photochemistry

Indexed keywords

HYDROGEN BONDS; OLEFINS; PHOTOCHEMICAL REACTIONS; SYNTHESIS (CHEMICAL);

BUILDING BLOCKS;

AROMATIC COMPOUNDS;

3,4 DIHYDRO 2 PYRIDONE DERIVATIVE; ACETOPHENONE; ALDEHYDE; BENZALDEHYDE; BENZOPHENONE; ETHER DERIVATIVE; GLYOXYLIC ACID DERIVATIVE; KETONE; LACTAM; OXETANE; OXETANE DERIVATIVE; PIPERIDINE DERIVATIVE; PYRIDONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMISTRY; CHIRALITY; ENANTIOMER; HYDROGEN BOND; PHOTOCHEMISTRY; RADIATION EXPOSURE; STEREOCHEMISTRY; SYNTHESIS; ULTRAVIOLET RADIATION;

ALDEHYDES; ETHERS, CYCLIC; KETONES; PHOTOCHEMISTRY; PIPERIDINES; PYRIDONES; ULTRAVIOLET RAYS;

EID: 0035887430     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3765(20011015)7:20<4512::AID-CHEM4512>3.0.CO;2-H     Document Type: Article

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