6229-00-1Relevant articles and documents
Silicon-carbon unsaturated compounds. 62. Reactions of silenes produced thermally from pivaloyl- and adamantoyltris(trimethylsilyl)silane with mono(silyl)acetylenes
Naka, Akinobu,Ishikawa, Mitsuo
, p. 248 - 255 (2000)
Thermolysis of pivaloyltris(trimethylsilyl)silane (1a) with tert-butyldimethylsilylacetylene at 120°C gave 2-tert-butyl-3-tert-butyldimethylsilyl-2-trimethylsiloxy-1,1-bis(trimethylsilyl) -1-silacyclobut-3-ene (2a). Similar treatment of adamantoyltris(trimethylsilyl)silane (1b) at 120°C produced 2-adamantyl-3-tert-butyldimethylsilyl-2-trimethylsiloxy-1,1-bis(trimethylsilyl)- 1-silacyclobut-3-ene (2b). Thermolysis of 1a with tert-butyldimethylsilylacetylene at 160°C, however, gave 1-tert-butyl-1-(tert-butyldimethylsilyl)-3-[(trimethylsiloxy)bis(trimethylsilyl) silyl]-1,2-propadiene (3a), along with 1:2 adduct (4a). Similar reaction of 1b gave 1-adamantyl-1-(tert-butyldimethylsilyl)-3-[(trimethylsiloxy)bis(trimethylsilyl) silyl]-1,2-propadiene (3b) similar to 3a, together with 1:2 adduct (4b). Thermolysis of 1a and 1b in the presence of dimethylphenylsilylacetylene or triphenylsilylacetylene at 120°C produced [2 + 2] cycloadducts arising from the reaction of silenes generated thermally from 1a and 1b with mono(silyl)acetylenes analogous 2a and 2b, along with small amounts of 1:2 adducts. At 160°C, the similar treatment of 1a and 1b afforded propadiene derivatives arising from the ring opening reactions of [2 + 2] cycloadducts, in addition to 1:2 adducts.
Enantioselective Iridium-Catalyzed Allylation of Acetylenic Ketones via 2-Propanol-Mediated Reductive Coupling of Allyl Acetate: C14-C23 of Pladienolide D
Brito, Gilmar A.,Jung, Woo-Ok,Yoo, Minjin,Krische, Michael J.
supporting information, p. 18803 - 18807 (2019/11/19)
Highly enantioselective catalytic reductive coupling of allyl acetate with acetylenic ketones occurs in a chemoselective manner in the presence of aliphatic or aromatic ketones. This method was used to construct C14-C23 of pladienolide D in half the steps previously required.
Using triethynylphosphine ligands bearing bulky end caps to create a holey catalytic environment: Application to gold(I)-catalyzed alkyne cyclizations
Ochida, Atsuko,Ito, Hideto,Sawamura, Masaya
, p. 16486 - 16487 (2007/10/03)
The synthesis, properties and catalytic uses of phosphinoalkynes bearing bulky end caps at the alkyne termini, that is, tris[(triarylsilyl)ethynyl]phosphines are reported. The most salient feature of the new phosphines is the holey molecular shape possess
