Affiliation:
1. Institut für Anorganische Chemie der Universität München
Abstract
Abstract
1-Organyl-1-boracyclopentanes react with alkynyltrimethylstannanes to give 1-bora-cyclohexylid(2)enes as the only products. The analogous reaction with methylbis (tert-butyl)borane leads to a nonstatistical distribution of organoboration products. Structure and stereochemistry of the new compounds are discussed on the basis of methanolysis reactions and 1H, 11B and 13C NMR data.
Cited by
13 articles.
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1. Reactivity of 1-boraadamantanes towards bis(trialkylstannyl)ethynes. First examples of 3-boratricyclo[5.3.1.13,9]dodecanes, and the molecular structure of a tetraalkyldiboroxane;Journal of Organometallic Chemistry;2003-12
2. Novel rearrangements and formation of 2,5-dihydro-1,2,5-oxoniastannaboratolesvia methanolysis of zwitterionic η2-(alkyn-1-yl-borate)alkenyltin compounds;Chemistry of Heterocyclic Compounds;1999-09
3. 1,1-organoboration of alkynylsilicon, -germanium, -tin and -lead compounds;Coordination Chemistry Reviews;1995-11
4. 1,1-Organoboration of tri-1-alkynyltin compounds: novel triorganotin cations, stannoles, 3-stannolenes and 1-stanna-4-bora-2,5-cyclohexadienes;Inorganica Chimica Acta;1994-06
5. Organoborierung von alkinylstannanen;Journal of Organometallic Chemistry;1988-06