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Volumn , Issue 8, 2001, Pages 1203-1214

Hydroxy-group directivity in the regioselective and diastereoselective [2+2] photocycloaddition (Paternò-Büchi reaction) of aromatic carbonyl compounds to chiral and achiral allylic substrates: The preparation of oxetanes with up to three stereogenic centers as synthetic building blocks

(2) Adam, W a Stegmann, V R a

a UNIVERSITY OF WÜRZBURG (Germany)

Author keywords

1,3 allylic strain; Diastereoselective synthesis; Hydrogen bonding; Patern B chi reaction

Indexed keywords

ALCOHOLS; AROMATIC COMPOUNDS; CARBONYLATION; HYDROGEN BONDS; SOLVENTS;

DIASTEREOSELECTIVITY; PHOTOCYCLOADDITIONS;

SYNTHESIS (CHEMICAL);

ACETOPHENONE; BENZALDEHYDE; BENZOPHENONE; CARBONYL DERIVATIVE; OXETANE DERIVATIVE;

ARTICLE; CHIRALITY; CYCLIZATION; DIASTEREOISOMER; HYDROGEN BOND; MOLECULAR DYNAMICS; PHOTOCHEMISTRY; REACTION ANALYSIS; SYNTHESIS;

EID: 0034963609 PISSN: 00397881 EISSN: None Source Type: Journal
DOI: 10.1055/s-2001-15070 Document Type: Article

Times cited : (47)

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