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1997 (1)
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 Title    Silaheterocyclen, XXXIII [1, 2]: Cycloadditions-Reaktionen des 1.1-Dichlor-2-neopentyIsilaethens mit Pentafulvenen  
 Abstract    ilaheterocycles, X X X III [1, 2]: C y c lo a d d itio n R e a c tio n s of 1 .1 -D ic h lo ro -2 -n eo p e n ty lsilen e w ith P e n ta fu lv e n e s N o rb e rt A u n er* , C la u s-R ü d ig e r H e ik e n w ä ld e r The reaction between in situ formed l,l-dichloro-2-neopentyl-l-silene, Cl2Si=CHCH2rBu (2), and 1,1-dimethylpentafulvene (5) leads to the formation of exo/endo-isomeric [4+2] cy-cloadducts 9 and [2+2] stereoisom ers 10 in good yields. NMR spectroscopic investigations of the product mixture prove the different modes of the silene cycloaddition reactions ([4+2] vs [2+2] addition). Treatment of 9 and 10 with LiA lH 4 and LiMe yield the stereo-and regioisomeric derivati­ ves (LiAlH 4: 16. 17; MeLi: 18, 19), whereas PhMgBr reacts with 10 to give only the mono substitution, the [4+2] com pound 20, and the diphenylated silacyclobutane 21. The reactions of silene 2 with pentafulvenes 6 -8 lead to similar results. 
  Reference    Z. Naturforsch. 52b, 500—514 (1997); eingegangen am 19. Dezember 1996 
  Published    1997 
  Keywords    Cycloaddition Reactions, Neopentylsilene, Pentafulvenes, NMR Spectra 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0500.pdf 
 Identifier    ZNB-1997-52b-0500 
 Volume    52