Enantioselective total syntheses of (-)-7βH-eudesmane-4α,11-diol and (+)-ent-7βH-eudesmane-4α,11-diol

Journal of Natural Products

Volumn 61, Issue 1, 1998, Pages 22-28

  Shimoma, Fumito ^a   Kondo, Hisao ^a   Yuuya, Saori ^a   Suzuki, Toshio ^a   Hagiwara, Hisahiro ^a   Ando, Masayoshi ^a  

^a NIIGATA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CARVONE; EUDESMANE DERIVATIVE; NATURAL PRODUCT;

ARTICLE; DRUG ISOLATION; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; MEDICINAL PLANT; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PAKISTAN; STEREOCHEMISTRY;

PLUCHEA;

EID: 0031908943     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np9702906     Document Type: Article

References (9)

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2. Ando, M.; Arai, K.; Isogai, K. J. Nat. Prod. 1994, 57, 1189-1199.
3. Hortmann, A. G.; Martinelli, J. E.; Wang, Y.-S. J. Org. Chem. 1969, 34, 732-736, and references therein.
4. McQuillin, F. J. J. Chem. Soc. 1965, 528-534.
5. We noticed previously that this procedure is convenient for dehydration of the hydroxyl group of acid- or base-sensitive compounds and applied it to the synthesis of (+)-arubusculin A and its related compounds; Ando, M.; Isogai, K.; Azami, H.; Hirata, N.; Yanagi, Y. J. Nat. Prod. 1991, 54, 1017-1024.
6. 2
7. Sharpless, K. B.; Michaelson, R. C. J. Am. Chem. Soc. 1973, 95, 6136-6137.
8. Howe, R.; McQuillin, F. J. J. Chem. Soc. 1955, 2423-2427.
9. Marshall, J. A., Pike, M. T. J. Org. Chem. 1968, 33, 435-437, and references therein.