mycalamide A

 

Topic mentions per year

Topic mentions per year

1993-2012
02419932012

Papers overview

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2012
2012
Mycalamide A, a marine natural compound previously isolated from sponges, is known as a protein synthesis inhibitor with potent… (More)
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2009
2009
Structures have been obtained for the complexes that triacetyloleandomycin and mycalamide A form with the large ribosomal subunit… (More)
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2006
2006
The details of a convergent total synthesis of (+)-mycalamide A are described. Yb(OTf)3-TMSCl-catalyzed cross-aldol reaction… (More)
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2005
2005
This communication describes a concise and efficient total synthesis of mycalamide A by the convergent coupling of pederic acid… (More)
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2005
2005
Intraspecific variation in the composition of three cytotoxic secondary metabolites from the New Zealand marine sponge Mycale… (More)
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2001
2001
The marine sponge metabolites mycalamide A (myca-lamide) and pateamine are extremely cytotoxic. While mycalamide has been shown… (More)
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2000
2000
A new mycalamide, mycalamide D (3), has been isolated from the New Zealand marine sponge Mycale sp. This new metabolite, in which… (More)
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2000
2000
The new cytotoxic compounds, mycalamides C (3) and D (4), have been isolated from the marine sponge Stylinos n. sp., along with… (More)
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2000
2000
A novel, polyoxygenated, pyranose ring containing 16-membered macrolide peloruside A (1) exhibiting cytotoxic activity in the… (More)
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2000
2000
[formula: see text] The final stages of a total synthesis of mycalamide A are described. A key step is the aldol reaction… (More)
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