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Volumn 15, Issue 46, 2009, Pages 12807-12818

Total synthesis and biological evaluation of (+)-neopeltolide and its analogues

Author keywords

Macrocycles; Natural products; Ring closing metathesis; Suzuki Miyaura coupling; Total synthesis

Indexed keywords

MACROCYCLES; NATURAL PRODUCTS; RING CLOSING METATHESIS; SUZUKI-MIYAURA COUPLING; TOTAL SYNTHESIS;

EID: 71549145618     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200901675     Document Type: Article
Times cited : (65)

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    • We thank Professor Taber for suggesting the use of his method for the synthesis of 15
    • We thank Professor Taber for suggesting the use of his method for the synthesis of 15.
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    • Our attempts to prepare lactone-derived enol phosphate (or its tri- flate counterpart) corresponds to 8 were unrewarding
    • Our attempts to prepare lactone-derived enol phosphate (or its tri- flate counterpart) corresponds to 8 were unrewarding.
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    • The yield of 46 was lower (56 % yield from 34) when performing the ring-closing metathesis in toluene at a concentration of 20 mM
    • The yield of 46 was lower (56 % yield from 34) when performing the ring-closing metathesis in toluene at a concentration of 20 mM.
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    • The corresponding methyl ester was also inactive at 100 nM
    • The corresponding methyl ester was also inactive at 100 nM.


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