VM 55599

Known as: 1H,5H-5a,12b-(Iminoethano)pyrrolizino(1,2-b)carbazol-14-one, 2,3,6,11,12,12a-hexahydro-1,12,12-trimethyl-, (1R-(1alpha,5abeta,12abeta,12bbeta))-, VM-55599, VM55599 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1993-2008
0119932008

Papers overview

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2008
2008
The secondary metabolites VM55599 (4) and preparaherquamide (5) have been identified by LC-MS(n) analysis as natural metabolites… (More)
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2002
2002
The first asymmetric biomimetic total synthesis of VM55599 (13) has been achieved utilizing an intramolecular Diels-Alder… (More)
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2001
2001
The 3-ylidenepiperazine-2,5-diones 16 and 39 and 5-acyloxy-2(1H)-pyrazinones 17 can serve as starting materials for the Diels… (More)
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1998
1998
A potentially bio-mimetic Diels-Alder cyclization to construct the bicyclo[2.2.2] ring system common to the paraherquamides… (More)
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1993
1993
Four novel metabolites of a Penicillium strain, IMI 332995, which has previously been reported to produce paraherquamide and a… (More)
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