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Volumn 15, Issue 21, 1996, Pages 4531-4536

Synthesis and reactions of a stannanethione derived from a kinetically stabilized diarylstannylene

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EID: 0001655683     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om960449u     Document Type: Article
Times cited : (43)

References (52)
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    • For reviews, see: (a) Tsumuraya, T.; Batcheller, S. A.; Masamune, S. Angew. Chem., Int. Ed. Engl. 1991, 30, 902. (b) Barrau, J.; Escudié, J.; Satgé, J. Chem. Rev. 1990, 90, 283. (c) Raabe, G.; Michl, J. The Chemistry of Organosilicon Compounds; Wiley-Interscience: New York, 1989; p 1015. (d) West, R. Angew. Chem., Int. Ed. Engl. 1987, 26, 1201. (e) Brook, A. G.; Baines, K. M. Adv. Organomet. Chem. 1986, 25, 1. (f) Raabe, G.; Michl, J. Chem. Rev. 1985, 85, 419. (g) Driess, M. Adv. Organomet. Chem. 1996, 39, 193. (h) Okazaki, R.; West, R. Adv. Organomet. Chem. 1996, 39, 232. (i) Baines, K. M.; Stibbs, W. G. Adv. Organomet. Chem. 1996, 39, 275.
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  • 29
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    • For preliminary results, see ref 17a
    • For preliminary results, see ref 17a.
  • 42
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    • note
    • 23
  • 48
    • 85033865831 scopus 로고    scopus 로고
    • For experimental details of the reaction of stannylene 2a with elemental selenium, see ref 16b
    • For experimental details of the reaction of stannylene 2a with elemental selenium, see ref 16b.
  • 51
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    • note
    • Both 11 and 12 were found to be cis and trans isomers. Although the stereochemistry of two ligands on the tin and a phenyl group in them was not confirmed, a less polar compound on silica gel is designated as a in each case.


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