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1.
Tsunehisa Hirashita Yousuke Hayashi Kazuma Mitsui Shuki Araki 《Tetrahedron letters》2004,45(16):3225-3228
Vinyl and methylindium ate complexes (indates) were prepared and both the tendency of immigration and regioselectivity toward cinnamyl bromide were investigated. The vinyl group was more preferably transferred than the Me group, giving a regioisomeric mixture of SN2 and SN2′ products. The ratio of SN2/SN2′ selectivity can be controlled by solvents; in the presence of polar solvents, such as N-butylpyrrolidone (NBP) and THF, the SN2′ product was mainly obtained, whereas the SN2 product was selectively prepared in solutions containing hexane. The vinylindium compound, generated by the reaction of allylic-type diindium reagents with imine, was also converted to the corresponding vinyl indate, which was allowed to react with allyl chloride to give a three-component coupling product. 相似文献
2.
Gallium(III) and indium(III) halides were found to mediate the condensation of cyclopropenes and nitriles to give pyrrole derivatives in moderate yields. When excess nitrile was present, diazepine was also formed. 相似文献
3.
Tsunehisa Hirashita Yusuke Daikoku Hitoshi Osaki Mamiko Ogura Shuki Araki 《Tetrahedron letters》2008,49(37):5411-5413
Methylenecyclopropanes carrying a hydroxymethyl group at the ring underwent stereoselective allylindation with allylindium sesquiiodide to afford the allylated products, in which the allyl group was delivered at the external sp2 carbon via cyclopropylindium intermediates. The reaction of ethyl 2-cyclopropylideneacetate and triallylindium afforded the 1,4-adduct along with dimeric products. 相似文献
4.
Hirashita T Kambe S Tsuji H Araki S 《Chemical communications (Cambridge, England)》2006,(24):2595-2597
In the presence of InI, Ni(acac)2 and PPh3, several 1,3-dienes were reacted with two molecules of aldehyde to give the corresponding 1,4- and 1,6-diols. The regioselectivity of the 1,4-/1,6-diol was efficiently regulated by the addition of water; the 1,6-diol was obtained selectively in dry THF, whereas the 1,4-diol was obtained predominantly in DMI containing a small amount of water. 相似文献
5.
Hirashita T Akutagawa K Kamei T Araki S 《Chemical communications (Cambridge, England)》2006,(24):2598-2600
The Ni-catalysed reaction of triallylindium with internal alkynes underwent bis-allylation to afford octa-1,4,7-trienes in high yield. 相似文献
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Reactions of electron-deficient alkenes with dibromomethylene compounds activated by cyano and ester groups were promoted by LiI or tetrabutylammonium bromide to afford the corresponding cyclopropanes in high yields. 相似文献
8.
Yasuo Butsugan Akihiko Yamashita Shuki Araki 《Journal of organometallic chemistry》1985,287(1):103-108
The reaction of dipotassium tetracarbonylferrate with various allylic phosphates and halides gives 1,3-dienetricarbonyliron complexes. The formation of the complexes is highly stereoselective depending on the geometry of the allylic compounds used. 相似文献
9.
The aromatic character of the meso-ionic sesquifulvalene (2) is demonstrated by six electrophilic substitution reactions on the cyclopentadienide ring. 相似文献
10.
Samarium(II)-induced coupling of acid chlorides with allylic halides gave diallylated tertiary alcohols. Monoallylated allylic ketones could not be obtained. 相似文献