2,2-dimethyl-2H-pyran-derived alkaloids I. Practical synthesis of acronycine and benzo[b]acronycine and their biological properties-Reference-Cited by-同舟云学术

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2,2-dimethyl-2H-pyran-derived alkaloids I. Practical synthesis of acronycine and benzo[b]acronycine and their biological properties

Published:2008-09 Issue:9 Volume:31 Page:1087-1093
ISSN:0253-6269
Container-title:Archives of Pharmacal Research
language:en
Short-container-title:Arch. Pharm. Res.

Author:

Motiur Rahman A. F. M.,Liang Jing Lu,Lee Seung Ho,Son Jong Keun,Jung Mi-Ja,Kwon Youngjoo,Jahng Yurngdong

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Drug Discovery,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/s12272-001-1273-7.pdf

Reference45 articles.

1. Anand, R. C. and Selvapalam, N., A practical regiospecific approach towards acronycine and related alkaloids. Chem. Commun., 199–200 (1996).

2. Bandaranayake, W. M., Crombie, L., and Whiting, D. A., Novel methods for the synthesis of 2-2-dimethylchromens. Chem. Commun., 970–971 (1969).

3. Bandaranayake, W. M., Crombie, L., and Whiting, D. A., Pyridine-catalysed chromenylation of mono-chelated metadihydric phenols with mono-, sesqui-and di-terpene aldehydes: synthesis of rubranine and flemingins A-, B-and C-methyl ethers. J. Chem. Soc. C, 804–810 (1971).

4. Beck, J. R., Kwok, R., Booher, R. N., Brown, A. C., Patterson, L. E., Pranc, P., Rockley, B., and Pohland, A., Synthesis of acronycine. J. Am. Chem. Soc., 90, 4706–4710 (1968).

5. Blechert, S., Fichter, K.-E., Lindner, J., and Winterfeldt, E., Cyclisierungen zu 9,11-disubstituierten Acronycin-Derivaten. Liebigs Ann. Chem., 503–511 (1980).

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