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Org Biomol Chem ; 11(20): 3393-9, 2013 May 28.
Article in English | MEDLINE | ID: mdl-23563191

ABSTRACT

Spirolactones, spirotetrahydrofurans, and spiropyrrolidines containing a vicinal cis-diol adjacent to the spiro-carbon center are prepared by one-pot epoxidation/spirocyclization of cyclohex-2-en-1-ols bearing an ester, alcohol, or amide functional side chain at the C(3) position of the ring.


Subject(s)
Cyclohexanols/chemical synthesis , Epoxy Compounds/chemical synthesis , Spiro Compounds/chemical synthesis , Crystallography, X-Ray , Cyclization , Cyclohexanols/chemistry , Epoxy Compounds/chemistry , Models, Molecular , Molecular Structure , Spiro Compounds/chemistry , Stereoisomerism
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