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Volumn 60, Issue 24, 2004, Pages 5237-5252

Rubrenolide, total synthesis and revision of its reported stereochemical structure

Author keywords

Epoxy diazomethyl ketone; Lactone; Rubrenolide

Indexed keywords

LACTONE DERIVATIVE; RUBRENOLIDE; UNCLASSIFIED DRUG;

EID: 2542476272     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.04.037     Document Type: Article
Times cited : (29)

References (39)
  • 24
    • 2542485254 scopus 로고    scopus 로고
    • 3indicatedaneeof91%
    • 3 indicated an ee of 91%
  • 27
    • 2542451699 scopus 로고    scopus 로고
    • 3 Rubrynolide was hydrogenated to give dihydrorubrenolide (see Section 5)
    • 3 Rubrynolide was hydrogenated to give dihydrorubrenolide (see Section 5)
  • 34
    • 2542420692 scopus 로고    scopus 로고
    • Minimum energy structures were generated by semi-empirical MOPAC PM3 calculations and carried out by Dr G.J.A. Ariaans (Synthon, Nijmegen, The Netherlands)
    • Minimum energy structures were generated by semi-empirical MOPAC PM3 calculations and carried out by Dr G.J.A. Ariaans (Synthon, Nijmegen, The Netherlands)
  • 35
    • 0004030018 scopus 로고
    • There are examples of complete control of stereochemistry when both components in the Aldol condensation are chiral, see:
    • There are examples of complete control of stereochemistry when both components in the Aldol condensation are chiral, see: Dongala E.B., Dull D.L., Mioskowski C., Solladié G. Tetrahedron Lett. 1973;4983
    • (1973) Tetrahedron Lett. , pp. 4983
    • Dongala, E.B.1    Dull, D.L.2    Mioskowski, C.3    Solladié, G.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.