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Volumn 29, Issue 48, 1988, Pages 6199-6202

Chirality transfer from silicon to carbon: use of optically pure cyclic silanes with a binaphthalene chiral unit

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0000335631     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)82304-7     Document Type: Article
Times cited : (40)

References (33)
  • 21
    • 33845555696 scopus 로고
    • Silanes in organic synthesis. 18. Preparation and reactivity of optically active vinyl- and dienylsilanes
    • (1982) Organometallics , vol.1 , pp. 1449
    • Daniels1    Paquette2
  • 25
    • 0000203874 scopus 로고
    • There are two examples of high diastereoselectivity: 74% de, in the carboxylation of the (1-lithiobenzyl)methyl(1-naphthyl)phenylsilane
    • (1970) J. Am. Chem. Soc. , vol.92 , pp. 7567
    • Brook1    Duff2    Anderson3
  • 27
    • 84918160406 scopus 로고    scopus 로고
    • The substitution of a mesityl group for the 1-naphthyl group improved the de from 0% to 20%, thus indicating that the choice of the chiral unit is extremely important for high selectivity.
  • 28
    • 77956224943 scopus 로고
    • New and Improved Synthesis of Optically Pure (R)-and (S)-2,2′-Dimethyl-1, 1′-binaphthyl and Related Compounds
    • (1985) Synthesis , pp. 317
    • Maigrot1    Mazaleyrat2
  • 30
    • 84918160405 scopus 로고    scopus 로고
    • 4, the overall yield of 6 in this process is ∼15% higher.
  • 31
    • 0002957257 scopus 로고
    • THE TITANIUM TETRACHLORIDE-PROMOTED REACTION OF KETENE ALKYL TRIALKYLSILYL ACETALS WITH ACETALS OR AN ORTHOFORMATE
    • (1976) Chemistry Letters , vol.163 , pp. 769
    • Saigo1    Osaki2    Mukaiyama3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.