muricatacin

Known as: 2(3H)-Furanone, dihydro-5-(1-hydroxytridecyl)-, (R-(R*,R*))- 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1998-2014
01219982014

Papers overview

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2014
2014
Efficient stereoselective total synthesis of (+)-muricatacin (1) and (+)-epi-muricatacin (8) was accomplished from commercially… (More)
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2010
2010
A chiron approach strategy toward the total synthesis of (+)-muricatacin and (+)-5-epi-muricatacin starting from commercially… (More)
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Review
2007
Review
2007
Synthetic studies of annonaceous acetogenins starting from (-)-muricatacin (1a) or (+)-muricatacin are described, involving… (More)
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2007
2007
[reaction: see text] An efficient oxidative lactonization of 1,4-diols in acetone is accomplished by the well-defined ruthenium… (More)
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2006
2006
A divergent approach to the 7-oxa (-)-muricatacin analogue 2, the corresponding (+)-enantiomer ent-2 and the furanolactone 3 is… (More)
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2006
2006
A short and highly efficient route to both enantiomers of muricatacin as well as the C-5-epimer has been developed. The key to… (More)
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2005
2005
Four new monotetrahydrofuranic Annonaceous acetogenins, montalicins G (1) and H (2) and monlicins A (3) and B (4), and two new… (More)
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1998
1998
Four stereoisomers of muricatacin 1a-d were prepared by the reaction of corresponding aldehydes 4a-d, which in turn were prepared… (More)
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