Title of article :
Synthesis of (3R,4S,5S,9S)-3,5,9-trihydroxy-4-methylundecanoic acid δ-lactone
Author/Authors :
Chakraborty، نويسنده , , Tushar K. and Goswami، نويسنده , , Rajib K.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2004
Pages :
3
From page :
7637
To page :
7639
Abstract :
Radical-mediated opening of a chiral trisubstituted epoxy alcohol using cp2TiCl furnished the ‘2-methyl-1,3-diol’ moiety with the desired stereochemistry, which led to a total synthesis of (3R,4S,5S,9S)-3,5,9-trihydroxy-4-methylundecanoic acid δ-lactone 1.
Keywords :
Epoxide opening , 2-Methyl-1 , 3-diol , (3R , 5S , 4S , 9S)-3 , 5 , ?-Lactone , 9-Trihydroxy-4-methylundecanoic acid , Sharpless kinetic resolution
Journal title :
Tetrahedron Letters
Serial Year :
2004
Journal title :
Tetrahedron Letters
Record number :
1843480
Link To Document :
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