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Volumn 49, Issue 10, 2008, Pages 1601-1604

A formal convergent synthesis of (+)-trans-solamin

Author keywords

Bromohydrin; NBS; Pummerer ene reaction; Sulfoxide; trans Solamin

Indexed keywords

ACETOGENIN; BENZETHONIUM CHLORIDE; CARBON;

EID: 38949198642     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.01.046     Document Type: Article
Times cited : (12)

References (40)
  • 1
    • 0032891112 scopus 로고    scopus 로고
    • For reviews of annonaceous acetogenins, see:
    • For reviews of annonaceous acetogenins, see:. Alali F.Q., Liu X.-X., and McLaughlin J.L. J. Nat. Prod. 62 (1999) 504-540
    • (1999) J. Nat. Prod. , vol.62 , pp. 504-540
    • Alali, F.Q.1    Liu, X.-X.2    McLaughlin, J.L.3
  • 19
    • 38949114651 scopus 로고    scopus 로고
    • note
    • The ene product indicated the presence of one major diastereomer, however, efforts were not made to separate or assign the configuration at the newly introduced stereogenic center of the major isomer since it was to be destroyed subsequently.
  • 31
    • 38949092598 scopus 로고    scopus 로고
    • note
    • 2O followed by esterification. Clear differences were observed in the chemical shifts for methylene protons of the Mom group; in the ester derived from 17 they resonate at δ 4.43 and 4.39, and at δ 4.6 and 4.5 in the ester derived from the epimer of 17.
  • 35
    • 0035793850 scopus 로고    scopus 로고
    • l-Selectride stereoselectively affords threo 1,2-diol derivatives upon reducing derivatives of α-hydroxy ketones, refer:
    • l-Selectride stereoselectively affords threo 1,2-diol derivatives upon reducing derivatives of α-hydroxy ketones, refer:. Arndt S., Emde U., Baurle S., Friedrich T., Grubert L., and Koert U. Chem. Eur. J. 7 (2001) 993
    • (2001) Chem. Eur. J. , vol.7 , pp. 993
    • Arndt, S.1    Emde, U.2    Baurle, S.3    Friedrich, T.4    Grubert, L.5    Koert, U.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.