I. DIELS-ALDER REACTIONS OF TRIMETHYL CYCLOPENTADIENYL STANNANE. II. PREPARATION AND DIELS-ALDER REACTIONS OF VINYLSULFOXIMINES.

I. DIELS-ALDER REACTIONS OF TRIMETHYL CYCLOPENTADIENYL STANNANE. II. PREPARATION AND DIELS-ALDER REACTIONS OF VINYLSULFOXIMINES.

In Part 1, the Diels-Alder adducts of trimethyl cyclopentadienylstannane (I.3) with maleic anhydride and fumaronitrile are prepared in 61% yield. The molecular structure of the adduct with maleic anhydride (1.6) is unequivocally established as 7-syn-trimethy1stannyl-endo- bicyclo[2.2.1]hept-5-enyl-2...

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Bibliographic Details
Main Author: REINEKE, KARL EDWARD, II.
Language:en
Published: The University of Arizona. 1983
Subjects:
Organotin compounds.
Organic compounds > Synthesis.
Diels-Alder reaction.
Online Access:http://hdl.handle.net/10150/186238

Internet

http://hdl.handle.net/10150/186238

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