Biosynthesis of brevianamides A and B: in search of the biosynthetic diels-alder construction (Q105173683)

http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2996255-6

main subject

Penicillium brevicompactum

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Juan F. Sanz-Cervera

1

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Tomasz Glinka

series ordinal

2

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Robert M. Williams

series ordinal

3

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publication date

25 July 2002

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published in

Tetrahedron

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volume

49

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issue

38

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page(s)

8471-8482

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Structure and absolute configuration of solanapyrone D: a new clue to the occurrence of biological Diels–Alder reactions

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The brevianamides: a new class of fungal alkaloid

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Studies in relation to biosynthesis. XLII. The structural elucidation and some aspects of the biosynthesis of the brevianamides-A and -E

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Isolation and structure (X-ray analysis) of marcfortine A, a new alkaloid from Penicillium roqueforti

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Effects of brevianamide A, its photolysis product brevianamide D, and ochratoxin A from two Penicillium strains on the insect pests Spodoptera frugiperda and Heliothis virescens

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Biosynthesis of the brevianamides: quest for a biosynthetic Diels-Alder cyclization

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Formation of peptide amides by peptidylglycine .alpha.-amidating monooxygenase: a new assay and stereochemistry of hydrogen loss

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Incorporation of aerobic oxygen into the hydroxyglycyl intermediate during formation of C-terminal peptide amides by peptidylglycine α-amidating monooxygenase (PAM)

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18O isotopic 13C NMR shift as proof that bifunctional peptidylglycine alpha-amidating enzyme is a monooxygenase

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Disposition of Mycophenolic Acid, Brevianamide A, Asperphenamate, and Ergosterol in Solid Cultures of Penicillium brevicompactum.

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Brevianamides A and B Are Formed Only After Conidiation Has Begun in Solid Cultures of Penicillium brevicompactum

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7 January 2021