Sakuraiova reakce (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sakuraiova reakce" in Czech language version.

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7doi.org

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1organic-chemistry.org

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doi.org

dx.doi.org

HOSOMI, Akira; SAKURAI, Hideki. Syntheses of γ,δ-unsaturated alcohols from allylsilanes and carbonyl compounds in the presence of titanium tetrachloride. Tetrahedron Letters. 1976-04-01, s. 1295–1298. ISSN 0040-4039. DOI 10.1016/S0040-4039(00)78044-0.
HOSOMI, Akira; ENDO, Masahiko; SAKURAI, Hideki. Allylsilanes as synthetic intermediates. ii. syntheses of homoallyl ethers from allylsilanes and acetals promoted by titanium tetrachloride. Chemistry Letters. 1976-09-05, s. 941–942. ISSN 0366-7022. DOI 10.1246/cl.1976.941.
HOSOMI, Akira; SAKURAI, Hideki. Chemistry of organosilicon compounds. 99. Conjugate addition of allylsilanes to .alpha.,.beta.-enones. A New method of stereoselective introduction of the angular allyl group in fused cyclic .alpha.,.beta.-enones. Journal of the American Chemical Society. 1977-03-01, s. 1673–1675. ISSN 0002-7863. DOI 10.1021/ja00447a080.
HOSOMI, Akira. Characteristics in the reactions of allylsilanes and their applications to versatile synthetic equivalents. Accounts of Chemical Research. 1988-05-01, s. 200–206. ISSN 0001-4842. DOI 10.1021/ar00149a004.
FLEMING, Ian; DUNOGUÈS, Jacques; SMITHERS, Roger. The Electrophilic Substitution of Allylsilanes and Vinylsilanes. Organic Reactions. American Cancer Society, 2004, s. 57–575. ISBN 9780471264187. DOI 10.1002/0471264180.or037.02. (anglicky)
FLEMING, Ian. 2.2 - Allylsilanes, Allylstannanes and Related Systems. Redakce Trost Barry M.. [s.l.]: Pergamon, 1991-01-01. ISBN 9780080523491. DOI 10.1016/b978-0-08-052349-1.00041-x. Kapitola Allylsilanes, Allylstannanes and Related Systems, s. 563–593.
Shingo Yamasaki; Kunihiko Fujii; Reiko Wada; Motomu Kanai; Masakatsu Shibasaki. A General Catalytic Allylation Using Allyltrimethoxysilane. Journal of the American Chemical Society. 2002-06-01, s. 6536–6537. ISSN 0002-7863. DOI 10.1021/ja0262582. PMID 12047165.

nih.gov

ncbi.nlm.nih.gov

Shingo Yamasaki; Kunihiko Fujii; Reiko Wada; Motomu Kanai; Masakatsu Shibasaki. A General Catalytic Allylation Using Allyltrimethoxysilane. Journal of the American Chemical Society. 2002-06-01, s. 6536–6537. ISSN 0002-7863. DOI 10.1021/ja0262582. PMID 12047165.

organic-chemistry.org

Hosomi-Sakurai Reaction [online]. [cit. 2019-09-01]. Dostupné online.

sciencedirect.com

FLEMING, Ian. 2.2 - Allylsilanes, Allylstannanes and Related Systems. Redakce Trost Barry M.. [s.l.]: Pergamon, 1991-01-01. ISBN 9780080523491. DOI 10.1016/b978-0-08-052349-1.00041-x. Kapitola Allylsilanes, Allylstannanes and Related Systems, s. 563–593.

worldcat.org

HOSOMI, Akira; SAKURAI, Hideki. Syntheses of γ,δ-unsaturated alcohols from allylsilanes and carbonyl compounds in the presence of titanium tetrachloride. Tetrahedron Letters. 1976-04-01, s. 1295–1298. ISSN 0040-4039. DOI 10.1016/S0040-4039(00)78044-0.
HOSOMI, Akira; ENDO, Masahiko; SAKURAI, Hideki. Allylsilanes as synthetic intermediates. ii. syntheses of homoallyl ethers from allylsilanes and acetals promoted by titanium tetrachloride. Chemistry Letters. 1976-09-05, s. 941–942. ISSN 0366-7022. DOI 10.1246/cl.1976.941.
HOSOMI, Akira; SAKURAI, Hideki. Chemistry of organosilicon compounds. 99. Conjugate addition of allylsilanes to .alpha.,.beta.-enones. A New method of stereoselective introduction of the angular allyl group in fused cyclic .alpha.,.beta.-enones. Journal of the American Chemical Society. 1977-03-01, s. 1673–1675. ISSN 0002-7863. DOI 10.1021/ja00447a080.
HOSOMI, Akira. Characteristics in the reactions of allylsilanes and their applications to versatile synthetic equivalents. Accounts of Chemical Research. 1988-05-01, s. 200–206. ISSN 0001-4842. DOI 10.1021/ar00149a004.
Shingo Yamasaki; Kunihiko Fujii; Reiko Wada; Motomu Kanai; Masakatsu Shibasaki. A General Catalytic Allylation Using Allyltrimethoxysilane. Journal of the American Chemical Society. 2002-06-01, s. 6536–6537. ISSN 0002-7863. DOI 10.1021/ja0262582. PMID 12047165.