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Volumn 3, Issue 19, 2001, Pages 3057-3060

Highly diastereoselective synthesis of propargylic 1,2-anti-diol derivatives using α-alkoxypropargylstannanes

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; ALKYNE; BIOLOGICAL FACTOR; PROPANOL; PROPARGYL ALCOHOL; STANNANE; TIN DERIVATIVE;

EID: 0035922327     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol016536m     Document Type: Article
Times cited : (33)

References (30)
  • 3
    • 0003065849 scopus 로고
    • Trost, B. M., Ed.; Pergamon Press: Oxford
    • Yumamoto, H. In Comprehensive Organic Synthesis; Trost, B. M., Ed.; Pergamon Press: Oxford, 1991: Vol. 2, p 81.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 81
    • Yumamoto, H.1
  • 12
    • 0042773433 scopus 로고    scopus 로고
    • note
    • We have recently found that mixtures of propargyl-and allenyl-stannanes give essentially the same results in BuSnCl3-promoted reactions with aldehydes.
  • 13
    • 84984217585 scopus 로고    scopus 로고
    • note
    • 1H NMR chemical shifts in 1,2-diol systems (Landmann, B.; Hoffmann, R. W. Chem. Ber. 1987, 120, 331). Authentic samples of the syn disatereomers were obtained by addition of the lithiated 9a and 9b to the corresponding aldehydes.
  • 14
    • 84984217585 scopus 로고    scopus 로고
    • Authentic samples of the syn disatereomers were obtained by addition of the lithiated 9a and 9b to the corresponding aldehydes
    • 1H NMR chemical shifts in 1,2-diol systems (Landmann, B.; Hoffmann, R. W. Chem. Ber. 1987, 120, 331). Authentic samples of the syn disatereomers were obtained by addition of the lithiated 9a and 9b to the corresponding aldehydes.
    • (1987) Chem. Ber. , vol.120 , pp. 331
    • Landmann, B.1    Hoffmann, R.W.2
  • 24
    • 0042272323 scopus 로고    scopus 로고
    • note
    • KF/Celite does not cleave the alkynyl TMS group nor a secondary TBS ether even after 24 h.
  • 28
    • 0042272324 scopus 로고    scopus 로고
    • note
    • The details of the synthesis of aldehyde 15 will be reported elsewhere.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.