Total synthesis of hybocarpone

Angewandte Chemie - International Edition

Volumn 40, Issue 4, 2001, Pages 761-763

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

^a SCRIPPS RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Natural products; Oxidative coupling; Photochemistry; Quinones; Total synthesis

Indexed keywords

1,4 NAPHTHOQUINONE DERIVATIVE; HYBOCARPONE; NAPHTHAZARIN; NATURAL PRODUCT; QUINONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CYTOTOXICITY; DIMERIZATION; DRUG ISOLATION; DRUG STRUCTURE; PHOTOCHEMISTRY;

EID: 0035804382     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3773(20010216)40:4<761::AID-ANIE7610>3.0.CO;2-0     Document Type: Article

References (13)

1. Related to this compound (2) are naturally occuring cristazarin (3-ethyl-2-hydroxy-7-methoxynaptharzarin) and 6-methylcristazarin. Both previously isolated from cultured mycobiont of the lichen Cladonia cristatella
2. A thorough investigation of this photo-induced reaction and its intramolecular variant for the construction of novel molecular diversity is currently being conducted and will be reported in due course. For a precedent