A total synthesis of the epoxyquinone natural product cytosporin D

Tetrahedron

Volumn 69, Issue 30, 2013, Pages 6034-6040

  Vannada, Jagadeshwar ^a   Niehues, Lennart ^a,b   König, Burkhard ^b   Mehta, Goverdhan ^a  

^a UNIVERSITY OF HYDERABAD   (India)

^b UNIVERSITY OF REGENSBURG   (Germany)

Author keywords

Diels Alder reaction; Epoxyquinone natural products; Oxycylization; Stereoselective reduction; Wittig olefination

Indexed keywords

2 PRENYL 4 BENZOQUINONE; CYCLOPENTADIENE DERIVATIVE; CYTOSPORIN D; EPOXYQUINONE; NATURAL PRODUCT; QUINONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CRYSTAL STRUCTURE; CYCLIZATION; DIELS ALDER REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; ISOMERISM; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; RING OPENING; STEREOCHEMISTRY; WITTIG REACTION;

ALNUS;

EID: 84878955251     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.05.075     Document Type: Article

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