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Carbohydr Res


Title:"Chiron approach from D-mannitol to access a diastereomer of the reported structure of an acetogenin, an amide alkaloid and a sex pheromone"
Author(s):Chatterjee S; Manna A; Chakraborty I; Bhaumik T;
Address:"Department of Chemistry, Jadavpur University, Jadavpur, Kolkata, 700032, West Bengal, India. Department of Chemistry, Jadavpur University, Jadavpur, Kolkata, 700032, West Bengal, India. Electronic address: tanurimabhaumik@gmail.com"
Journal Title:Carbohydr Res
Year:2019
Volume:20181214
Issue:
Page Number:5 - 11
DOI: 10.1016/j.carres.2018.12.008
ISSN/ISBN:1873-426X (Electronic) 0008-6215 (Linking)
Abstract:"A short, simple and convenient chiron approach to (3R,4S,5R)-(-)-3,5-dihydroxy-4-decanolide, a hitherto unknown diastereomer of the reported structure of a naturally occurring acetogenin, (+)-polyporolide has been accomplished starting from a commercially available, inexpensive chiral pool molecule D-(+)-mannitol in nine efficient steps. An advanced intermediate synthesized from D-(+)-mannitol in six steps toward this end was further employed successfully to access two different natural products bearing two contiguous stereogenic centers. As a result, first chiron approach to formal total synthesis of an amide alkaloid, (4R,5R,2E)-4,5-dihydroxy-1-(piperidin-1-yl)dec-2-en-1-one and total synthesis of a male sex pheromone in parasitic Hymenoptera, (4R,5R)-(-)-5-hydroxy-4-decanolide have also been achieved"
Keywords:Acetogenins/*chemistry Alkaloids/*chemistry Amides/*chemistry Animals Hymenoptera Male Mannitol/*chemistry Sex Attractants/*chemistry Stereoisomerism Chiral pool molecule Chiral template Chiron approach D-(+)-mannitol Formal synthesis Total synthesis;
Notes:"MedlineChatterjee, Sandip Manna, Avrajit Chakraborty, Ipsita Bhaumik, Tanurima eng Netherlands 2018/12/28 Carbohydr Res. 2019 Feb 1; 473:5-11. doi: 10.1016/j.carres.2018.12.008. Epub 2018 Dec 14"

 
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