메뉴 건너뛰기




Volumn 62, Issue 7, 1997, Pages 1924-1933

Total synthesis of archaeal 36-membered macrocyclic diether lipid

Author keywords

[No Author keywords available]

Indexed keywords

FATTY ACID DERIVATIVE; MACROCYCLIC COMPOUND;

EID: 0030920075     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo962327h     Document Type: Article
Times cited : (76)

References (63)
  • 20
    • 0000411804 scopus 로고
    • Kates, M., Kushner, D. J., Matheson, A. T., Eds.; Elsevier: Amsterdam
    • (m) Kates, M. In The Biochemistry of Archaea (Archaeobacteria); Kates, M., Kushner, D. J., Matheson, A. T., Eds.; Elsevier: Amsterdam, 1993; p 261.
    • (1993) The Biochemistry of Archaea (Archaeobacteria) , pp. 261
    • Kates, M.1
  • 50
    • 8244239077 scopus 로고    scopus 로고
    • Benzylation under basic conditions such as NaH-benzyl halide in DMF or DMSO was not straightforward as migration of the TBDMS group was observed in ca. 30-40% yield
    • Benzylation under basic conditions such as NaH-benzyl halide in DMF or DMSO was not straightforward as migration of the TBDMS group was observed in ca. 30-40% yield.
  • 52
    • 8244237765 scopus 로고    scopus 로고
    • note
    • 13 The hydrogenation reactions proceeded smoothly using several BINAP-Ru-based catalysts; however, the diastereomeric purities of the product ii were less than 75% in our hands. Chemical equations presented.
  • 63
    • 8244235178 scopus 로고    scopus 로고
    • The diastereomeric excess was determined by the method of Noyori et al. (ref 13a)
    • The diastereomeric excess was determined by the method of Noyori et al. (ref 13a).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.