Facile β-trimethylstannyl promoted 1,5-hydride shifts in cyclooctyl and cyclodecyl systems

Chemical Communications

Volumn , Issue 4, 2000, Pages 309-310

  Glenn, Matthew P ^a   Penman, Kerry G ^a   Kitching, William ^a  

^a UNIVERSITY OF QUEENSLAND   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLODECYLMESYLATE; CYCLOOCTYLMESYLATE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; DEUTERON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; SYNTHESIS;

EID: 0034696368     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/a909463f     Document Type: Article

References (32)

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22. Large prisms of the trans-diol (we thank Dr P. Bernhardt for an X-ray structural analysis) were processed to a single stannane isomer (see Scheme 1) concluded to be the cis on the basis of argument presented in the text.
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30. We are unaware of solvolytic data for any other stereochemically defined, substituted cyclodecylsulfonate esters.
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