An efficient synthesis of novel tetrahydrochromeno[2,3-b]chromenes

Tetrahedron Letters

Volumn 51, Issue 28, 2010, Pages 3636-3638

  Devakaram, Ruth ^a   Black, David Stc ^a   Kumar, Naresh ^a  

^a UNIVERSITY OF NEW SOUTH WALES   (Australia)

Author keywords

Acid catalyzed dimerization; Flavene dimers; Tetrahydrochromeno 2,3 b chromenes

Indexed keywords

5 METHOXYFLAVENE DERIVATIVE; 6 METHOXYFLAVENE DERIVATIVE; CHROMENE DERIVATIVE; DIMER; FLAVONOID; TETRAHYDROCHROMENO[2,3 B]CHROMENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; DIMERIZATION; DRUG STRUCTURE; DRUG SYNTHESIS; REACTION ANALYSIS;

EID: 77954349631     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.05.025     Document Type: Article

References (8)

1. H. Adlercreutz Lancet Oncol. 3 2002 364 373
2. X. Ma, Y. Liua, and Y. Shi Chem. Biodivers. 4 2007 2172 2181
3. M.H.H. Nkunya, R. Waibel, and H. Achenbach Phytochemistry 34 1993 853 856
4. M. Deodhar, D. StC. Black, and N. Kumar Tetrahedron 63 2007 5227 5235
5. J.W. Clark-Lewis, and R.W. Jemison Aust. J. Chem. 21 1968 2247 2254
6. 2: C, 60.59; H, 4.13. Found: C, 60.82; H, 4.26.
7. 4: C, 60.59; H, 4.13. Found: C, 60.32; H, 4.13.
8. Crystallographic data for the structure of compound 4b have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC 769425. The X-ray crystal structure was obtained by Don Craig, Crystallography Laboratory, Analytical Centre, The University of New South Wales, Sydney, Australia.