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Miyaoka et al., 1998 - Google Patents

Total synthesis of constanolactone E, a marine eicosanoid from the alga constantinea simplex; absolute structure of constanolactone E

Miyaoka et al., 1998

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Document ID
5345136295087841371
Author
Miyaoka H
Shigemoto T
Yamada Y
Publication year
Publication venue
Heterocycles

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Synthesis of marine eicosanoid constanolactone E was achieved through the one-pot formation of chiral cyclopropane derivative (6) using the anion of allyl phenyl sulfone and chiral epoxy mesylate (5). The absolute structure of constanolactone E was determined as 1 …
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    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/26Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D307/30Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic System
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C-Si linkages
    • C07F7/18Compounds having one or more C-Si linkages as well as one or more C-O-Si linkages
    • C07F7/1804Compounds having Si-O-C linkages
    • C07F7/1812Compounds having Si-O-C linkages having (C1)a-Si-(OC2)b linkages, a and b each being >=1 and a+b = 4, C1 and C2 being hydrocarbon or substituted hydrocarbon radicals
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