1952
DOI: 10.1021/ja01122a510
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Preparation of Organopolysilanes

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1954
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Cited by 33 publications
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“…Although the first reports on the synthesis and derivatization of silyl anions was in the early 1930s, these compounds remained a laboratory curiosity [2] . This changed drastically with the pioneering works of Gilman et al ., who demonstrated that silyl anions are excellent buildings blocks for the synthesis of organosilanes [3,4] . Another milestone again achieved by Gilman and his group was the generation of the first oligosilyl anions 1 by reacting the corresponding oligosilane with methyllithium (Scheme 1).…”
Section: Methodsmentioning
confidence: 99%
“…Although the first reports on the synthesis and derivatization of silyl anions was in the early 1930s, these compounds remained a laboratory curiosity [2] . This changed drastically with the pioneering works of Gilman et al ., who demonstrated that silyl anions are excellent buildings blocks for the synthesis of organosilanes [3,4] . Another milestone again achieved by Gilman and his group was the generation of the first oligosilyl anions 1 by reacting the corresponding oligosilane with methyllithium (Scheme 1).…”
Section: Methodsmentioning
confidence: 99%
“…The mixture usually became warm at the start and In 1931 Blatt5 showed that isoxazolines gave no methane on treatment with methylmagnesium iodide and on this basis assigned structure I to them. The same year Blatt and Stone6 showed that isoxazolines derived from substituted chalcones had (1) This work was supported by a grant from the Research Corporation of New York for the purchase of a Perkin-Elmer 12C infrared spectrometer.…”
Section: Methodsmentioning
confidence: 99%
“…In particular, sterically encumbered organo-substituted silanides such as Li[Si(SiMetBu 2 ) 3 ] [7] or Na[SiMe(SitBu 3 ) 2 ] [8,9] proved to be very useful σ-donating ligands. First papers regarding the synthesis and reactivity of silanides M[SiR 3 ] were published by Gilman et al in the 1950s and 1960s [10,11]. Examples studied in detail were the triphenylsilanides M[SiPh 3 ] (M = Li, Na, K, Rb, Cs) [12,13].…”
Section: Introductionmentioning
confidence: 99%