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Volumn , Issue 15, 2004, Pages 2788-2790

An approach to the tricyclic lactone core of brasoside and related natural products

Author keywords

Cyclisations; Domino reactions; Natural products; Radical reactions; Stereoselective synthesis

Indexed keywords

BICYCLO COMPOUND; BRASOSIDE; IODINE; LACTONE DERIVATIVE; NATURAL PRODUCT; UNCLASSIFIED DRUG;

EID: 10844252915     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2004-835637     Document Type: Article
Times cited : (7)

References (17)
  • 3
    • 0011172266 scopus 로고
    • (a) This step is related to the proposed biosynthesis of the iridoids; for a review of iridoid chemistry, including biosynthetic aspects, see: El-Naggar, L. J.; Beal, J. L. J. Nat. Prod. 1980, 43, 649.
    • (1980) J. Nat. Prod. , vol.43 , pp. 649
    • El-Naggar, L.J.1    Beal, J.L.2
  • 5
    • 10844255115 scopus 로고    scopus 로고
    • DPhil Thesis; Oxford: UK
    • Ménard, M. DPhil Thesis; Oxford: UK, 2003.
    • (2003)
    • Ménard, M.1
  • 12
    • 10844230456 scopus 로고    scopus 로고
    • note
    • +]: 246.1494; found: 246.1491.
  • 13
    • 10844284843 scopus 로고    scopus 로고
    • note
    • 2], and 7.44 (=CHOH) ppm; irradiation of the olefinic proton at δ = 7.44 ppm led only to an enhancement at δ = 9.13 (=CHOh) ppm.
  • 14
    • 10844264764 scopus 로고    scopus 로고
    • note
    • 3OD. For further details, see ref. 4.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.