Probing the effect of allylic substitution on cyclic ammonium ylid rearrangements

Synlett

Volumn , Issue 4, 2010, Pages 664-666

  Sançon, Julien ^a   Sweeney, J B ^a  

^a UNIVERSITY OF READING   (United Kingdom)

Author keywords

Asymmetric; Catalytic; Lactacystin; Rearrangement; Ring closing metathesis

Indexed keywords

ALLYL COMPOUND; CARBOXYLIC ACID; CHEMICAL COMPOUND; CYCLIC AMMONIUM YLID; LACTACYSTIN; PROLINE; PYRROLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ALLYLIC REARRANGEMENT; ARTICLE; CHEMICAL STRUCTURE; STEREOCHEMISTRY; SYNTHESIS;

EID: 77955374490     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0029-1219348     Document Type: Article

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61. The relative stereochemistry of cis- and trans-10 was deduced from NOE experiments (alkene methine-ring methyl interactions), which will be reported elsewhere in due course.
62. The necessary analytical experiments to rigorously confirm these structural deductions are currently in progress.