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Volumn 118, Issue 29, 1996, Pages 7008-7009

Studies on the biosynthesis of paraherquamide A. Origin of the β-methylproline ring

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; BIOSYNTHESIS; DRUG PRODUCTS;

EID: 8944238473     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja961322z     Document Type: Article
Times cited : (30)

References (27)
  • 22
    • 0008349462 scopus 로고
    • For a leading reference on the method employed, see: Leete, E.; Bodem, G. B. J. Am. Chem. Soc. 1976, 98, 6321. These values were further corroborated by electrospray mass spectroscopy (see supporting information).
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 6321
    • Leete, E.1    Bodem, G.B.2
  • 23
    • 0003980030 scopus 로고
    • Chapman and Hall: London
    • (a) Herbert, R. B. The Biosynthesis of Secondary Metabolites; Chapman and Hall: London, 1981. Proline biosynthesis proceeds via reductive amination of glutamate semialdehyde which can be derived from either glutamate or ornithine; see:
    • (1981) The Biosynthesis of Secondary Metabolites
    • Herbert, R.B.1
  • 25
    • 0027241074 scopus 로고
    • Related examples of biosynthetic oxidative cyclizations of the isoleucine side chain methyl group can be found in polyoximic acid and (via allo-isoleucine) coronamic acid; see, respectively: (a) Hanessian, S.; Fu, J-M.; Tu, Y.; Isono, K. Tetrahedron Lett. 1993, 34, 4153.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 4153
    • Hanessian, S.1    Fu, J.-M.2    Tu, Y.3    Isono, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.