1027314-32-4Relevant articles and documents
Enantioselective synthesis of cis-7-methoxy-calamenene via Claisen rearrangement of an enzymatically resolved allyl alcohol
Brenna, Elisabetta,Dei Negri, Claudia,Fuganti, Claudio,Gatti, Francesco G.,Serra, Stefano
, p. 335 - 340 (2007/10/03)
An enantioselective synthesis of cis-7-methoxy-calamenene 1 has been accomplished through the following key-steps: (i) enzymatic resolution of the racemic allyl alcohol 3 to furnish the (R)-enantiomer (ee>99%); (ii) Claisen-orthoester rearrangement of 4 t