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Volumn 56, Issue 23, 2015, Pages 3600-3603

Atropurpuran - Missing biosynthetic link leading to the hetidine and arcutine C20-diterpenoid alkaloids or an oxidative degradation product?

Author keywords

Arcutines; Biosynthesis; Diterpenoid alkaloids; Hetidine; Oxidation

Indexed keywords

ALKALOID; ARCUTINE; ATROPURPURAN; DITERPENOID; GERANYLGERANYL PYROPHOSPHATE; HYDROXYL GROUP; HYDROXYLAMINE; UNCLASSIFIED DRUG;

EID: 84929952112     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2015.01.111     Document Type: Article
Times cited : (27)

References (27)
  • 8
    • 77951084072 scopus 로고    scopus 로고
    • For a computational analysis of diterpene biosynthetic pathways see: (b)
    • For a computational analysis of diterpene biosynthetic pathways see: (b) Y.J. Hong, and D.J. Tantillo J. Am. Chem. Soc. 132 2010 5375
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 5375
    • Hong, Y.J.1    Tantillo, D.J.2
  • 11
    • 84929949390 scopus 로고    scopus 로고
    • Several nitrogen sources (e.g., methylamine, ethylamine, β-aminoethanol and S-adenosylmethionine) have been proposed as precursors to the nitrogen atom found in the diterpene alkaloids (see Ref. 6c, p 87). However, to date, only l-serine has been identified as a nitrogen source, see Ref. 6b
    • Several nitrogen sources (e.g., methylamine, ethylamine, β-aminoethanol and S-adenosylmethionine) have been proposed as precursors to the nitrogen atom found in the diterpene alkaloids (see Ref. 6c, p 87). However, to date, only l-serine has been identified as a nitrogen source, see Ref. 6b.
  • 16
    • 84929947459 scopus 로고    scopus 로고
    • Previously Wang and Liang classified the arcutines as a rearranged class (C-II′) of the hetidines or hetisines, see Ref. 6c
    • Previously Wang and Liang classified the arcutines as a rearranged class (C-II′) of the hetidines or hetisines, see Ref. 6c.
  • 17
    • 80052174614 scopus 로고    scopus 로고
    • The overall transformation could also occur in a dyotropic manner, see, for example
    • The overall transformation could also occur in a dyotropic manner, see, for example, R.L. Davis, C.A. Leverett, D. Romo, and D.J. Tantillo J. Org. Chem. 76 2011 7167
    • (2011) J. Org. Chem. , vol.76 , pp. 7167
    • Davis, R.L.1    Leverett, C.A.2    Romo, D.3    Tantillo, D.J.4
  • 18
    • 70349347859 scopus 로고    scopus 로고
    • Université de Sherbrooke ()
    • C.Y. Legault CYLview, 1.0b 2009 Université de Sherbrooke (http://www.cylview.org)
    • (2009) CYLview, 1.0b
    • Legault, C.Y.1
  • 27
    • 84929948884 scopus 로고    scopus 로고
    • Data included in Supporting information
    • Data included in Supporting information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.