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Cycloadditions of o-quinone dimethides with p-quinol derivatives: regiocontrolled formation of anthracyclic ring systems
- Source :
-
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry . Feb2004, Vol. 45 Issue 8, p1793. 4p. - Publication Year :
- 2004
-
Abstract
- Regioselective cycloadditions between the cyclohexadienones 12–14 and the ortho-quinone dimethide 19, which is thermally generated from the corresponding 1,3-dihydro-1-methoxy-2,2-dioxide benzo[c]thiophene 27, are reported. The synthetic sequence provides rapid access to highly substituted anthracyclic system and may be of use for construction of the natural product (+)-rishirilide B. [Copyright &y& Elsevier]
- Subjects :
- *RING formation (Chemistry)
*CHEMICAL reactions
*ANTHRACYCLINES
*THIOPHENES
Subjects
Details
- Language :
- English
- ISSN :
- 00404039
- Volume :
- 45
- Issue :
- 8
- Database :
- Academic Search Index
- Journal :
- Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 12096661
- Full Text :
- https://doi.org/10.1016/j.tetlet.2003.12.114