Total synthesis of hamigerans: Part 2. Implementation of the intramolecular Diels - Alder trapping of photochemically generated hydroxy-o-quinodimethanes; strategy and completion of the synthesis

Angewandte Chemie - International Edition

Volumn 40, Issue 19, 2001, Pages 3679-3683

  Nicolaou, K C ^a,b   Gray, David ^a   Tae, Jinsung ^a,b  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Cycloaddition; Natural products; Photochemistry; Quinodimethanes; Total synthesis

Indexed keywords

EPIMERS;

MOLECULES; PHOTOCHEMICAL REACTIONS; SYNTHESIS (CHEMICAL);

ORGANIC COMPOUNDS;

BENZALDEHYDE; BENZYL DERIVATIVE; HAMIGERAN DERIVATIVE; HETEROCYCLIC COMPOUND; HYDROXY 2 QUINODIMETHANE DERIVATIVE; HYDROXYL GROUP; METHANE; NATURAL PRODUCT; QUINONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; BROMINATION; CHEMICAL REACTION; DRUG SYNTHESIS; HYDROXYLATION; MOLECULAR INTERACTION; PHOTOCHEMISTRY; STEREOCHEMISTRY; TECHNOLOGY;

EID: 0035476828     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3773(20011001)40:19<3679::AID-ANIE3679>3.0.CO;2-T     Document Type: Article

References (9)