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muricatacin

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

Papers overview

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2019
2019
BACKGROUND AND PURPOSE Colorectal cancer is one of the leading causes of cancer deaths in elderly people. The natural product… Expand
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2014
2014
Efficient stereoselective total synthesis of (+)-muricatacin (1) and (+)-epi-muricatacin (8) was accomplished from commercially… Expand
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2011
2011
Annonaceous acetogenins (AGEs) are potential phytochemicals of herbal medicines and exhibit a wide variety of biological… Expand
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Review
2007
Review
2007
  • Hidefumi Makabe
  • Bioscience, biotechnology, and biochemistry
  • 2007
  • Corpus ID: 31144920
Synthetic studies of annonaceous acetogenins starting from (-)-muricatacin (1a) or (+)-muricatacin are described, involving… Expand
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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… Expand
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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… Expand
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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… Expand
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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… Expand
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