Title of article :
A convenient asymmetric synthesis of the octalactin lactone
Author/Authors :
Sharma، نويسنده , , Anubha and Gamre، نويسنده , , Sunita and Roy، نويسنده , , Siddharth and Goswami، نويسنده , , Dibakar and Chattopadhyay، نويسنده , , Angshuman and Chattopadhyay، نويسنده , , Subrata، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2008
Pages :
4
From page :
3902
To page :
3905
Abstract :
A facile asymmetric synthesis of the octalactin lactone was developed staring from (R)-cyclohexylideneglyceraldehyde (1). The key step of the synthesis is an In-mediated diastereoselective crotylation of 1 in water, which furnished the building blocks with the required stereochemistry under operationally simple conditions. Their conversion to the appropriate intermediates, invertive esterification and a ring closing metathesis reaction furnished the target compound.
Keywords :
Octalactin , asymmetric synthesis , Crotylation , Chiral pool
Journal title :
Tetrahedron Letters
Serial Year :
2008
Journal title :
Tetrahedron Letters
Record number :
1859525
Link To Document :
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