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Synthesis 2003(7): 1087-1090
DOI: 10.1055/s-2003-39177
DOI: 10.1055/s-2003-39177
PAPER
© Georg Thieme Verlag Stuttgart ˙ New York
Hydroxycyclopentanone Derivatives from d-Mannose via Ring Closing Metathesis: An Improved Synthesis of a Key Intermediate of Tricyclo-DNA
Further Information
Received
26 February 2003
Publication Date:
09 May 2003 (online)
Publication History
Publication Date:
09 May 2003 (online)
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Abstract
A large scale, 10 step synthesis of cyclopentanone 1, starting from the chiral pool compound d-mannose, is described. The synthesis proceeds via a ring closing metathesis reaction as the key step in an overall yield of 23%. Cyclopentanone 1 is a central intermediate for the synthesis of tricyclo-DNA.
Key words
carbohydrates - metathesis - ring closure - ruthenium - ketones
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