Stereocontrol in ene-dimerisation and trimerisation of 1-trimethylsilyl-3- phenylcyclopropene

Tetrahedron Letters

Volumn 47, Issue 16, 2006, Pages 2839-2843

  Sheshenev, Andrey E ^a   Baird, Mark S ^b   Croft, Anna K ^b   Starikova, Zoya A ^c   Shashkov, Alexandre S ^d   Zhuze, Alexey L ^e   Bolesov, Ivan G ^a  

^a MOSCOW STATE UNIVERSITY   (Russian Federation)

^b BANGOR UNIVERSITY   (United Kingdom)

^c A N NESMEYANOV INSTITUTE OF ORGANOELEMENT COMPOUNDS   (Russian Federation)

^d N D ZELINSKY INSTITUTE OF ORGANIC CHEMISTRY   (Russian Federation)

^e ENGELHARDT INSTITUTE OF MOLECULAR BIOLOGY   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

1 TRIMETHYLSILYL 3 PHENYCYCLOPROPENE; DIMER; PROPYLENE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; DIMERIZATION; STEREOCHEMISTRY;

EID: 33644979241     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.12.111     Document Type: Article

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26. -1): 3025 m, 2955 s, 2897 m, 1693 s, 1602 m, 1492 m, 1446 s, 1248 s, 841 s, 756 s, 698 s.
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29. -1): 2953 s, 1496 s, 1448 s, 1409 s, 1250 s, 1034 s, 1024 s, 954 s, 846 s, 755 s, 695 s.
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33. C (125 MHz) including: -0.28+, -0.06+, 0.83+, 18.9+, 19.4+, 20.6, 26.9+, 28.4+, 29.6+, 32.9+, 115.2, 125.62+, 125.75+, 130.9, 136.5, 139.7, 140.4. Complete crystallographic data for compound 18 have been deposited with the Cambridge Crystallographic Data Centre (registration no. 283161).
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39. Bell's correction for tunnelling (R.P. Bell Trans. Faraday Soc. 55 1959 1 ) is not large in this case