메뉴 건너뛰기




Volumn 118, Issue 49, 1996, Pages 12469-12470

Axially chiral spirosilanes via catalytic asymmetric intramolecular hydrosilation

Author keywords

[No Author keywords available]

Indexed keywords

SILANE DERIVATIVE; SPIRO COMPOUND; THIOPHENE DERIVATIVE;

EID: 0030457105     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja962754c     Document Type: Article
Times cited : (125)

References (38)
  • 2
    • 0342553400 scopus 로고
    • Quite recently, the successful synthesis of chiral tetranuclear molecular squares has been reported
    • Quite recently, the successful synthesis of chiral tetranuclear molecular squares has been reported: Anderson, S.; Neidlein, U.; Gramlich, V.; Diederich, F. Angew. Chem., Int. Ed. Engl. 1995, 34, 1596.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 1596
    • Anderson, S.1    Neidlein, U.2    Gramlich, V.3    Diederich, F.4
  • 5
    • 0000209427 scopus 로고
    • A spiro building unit (racemic) has recently been applied to the synthesis of molecular squares: Small
    • A spiro building unit (racemic) has recently been applied to the synthesis of molecular squares: Small, J. H.; McCord, D. J.; Greaves, J.; Shea, K. J. J. Am. Chem. Soc. 1995, 117, 11588.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 11588
    • Small, J.H.1    McCord, D.J.2    Greaves, J.3    Shea, K.J.4
  • 19
    • 33744639870 scopus 로고    scopus 로고
    • 1 symmetry has been attained by way of the palladium-catalyzed intramolecular Heck-type arylations
    • 1 symmetry has been attained by way of the palladium-catalyzed intramolecular Heck-type arylations:
  • 22
    • 33744588757 scopus 로고    scopus 로고
    • For intramolecular hydrosilation, see
    • For intramolecular hydrosilation, see:
  • 23
    • 85027864497 scopus 로고
    • For asymmetric intramolecular hydrostlation of olefms, see
    • (a) Tamao, K.; Nakagawa, Y.; Ito, Y. Org. Synth 1995, 73, 94. For asymmetric intramolecular hydrostlation of olefms, see:
    • (1995) Org. Synth , vol.73 , pp. 94
    • Tamao, K.1    Nakagawa, Y.2    Ito, Y.3
  • 29
    • 33744682398 scopus 로고    scopus 로고
    • Throughout the paper, the absolute configuration of the silicon central chirality is shown first with a subscript Si. The difference in the absolute configurations of silicon between 1 and the precursors is merely due to the priority sequence.
    • Throughout the paper, the absolute configuration of the silicon central chirality is shown first with a subscript Si. The difference in the absolute configurations of silicon between 1 and the precursors is merely due to the priority sequence.
  • 30
    • 33744657717 scopus 로고    scopus 로고
    • The absolute configurations at the silicon atom in 1 are named according to the central chirality notation.1
    • The absolute configurations at the silicon atom in 1 are named according to the central chirality notation.1
  • 38
    • 33744686370 scopus 로고    scopus 로고
    • 2, 2 mol %; Rh/DIOP = 1:1), the reaction did not go to completion at -20 °C even after 7 days.
    • 2, 2 mol %; Rh/DIOP = 1:1), the reaction did not go to completion at -20 °C even after 7 days.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.