Stereochemical assignments of the chlorinated residues in victorin C

Amanda C. Durow; Craig Butts; Christine L. Willis

doi:10.1055/s-0029-1216910

Stereochemical assignments of the chlorinated residues in victorin C

Amanda C. Durow, Craig Butts, Christine L. Willis

School of Chemistry

Research output: Contribution to journal › Article (Academic Journal) › peer-review

7 Citations (Scopus)

Abstract

Victorins are cyclic pentapeptide natural products isolated from the fungus Cochliobus victoriae. Using a combination of synthesis and spectroscopic methods we have assigned the geometry of the vinyl chloride residue and determined the stereochemistry of the 5,5-dichloroleucine moiety.

Original language	English
Pages (from-to)	2954-2962
Number of pages	9
Journal	Synthesis (Germany)
Issue number	17
DOIs	https://doi.org/10.1055/s-0029-1216910
Publication status	Published - 2009

Keywords

Amino acids
Halogenation
Natural products
Spectroscopy
Stereoselective synthesis

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title = "Stereochemical assignments of the chlorinated residues in victorin C",

abstract = "Victorins are cyclic pentapeptide natural products isolated from the fungus Cochliobus victoriae. Using a combination of synthesis and spectroscopic methods we have assigned the geometry of the vinyl chloride residue and determined the stereochemistry of the 5,5-dichloroleucine moiety.",

keywords = "Amino acids, Halogenation, Natural products, Spectroscopy, Stereoselective synthesis",

author = "Durow, {Amanda C.} and Craig Butts and Willis, {Christine L.}",

year = "2009",

doi = "10.1055/s-0029-1216910",

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journal = "Synthesis (Germany)",

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T1 - Stereochemical assignments of the chlorinated residues in victorin C

AU - Durow, Amanda C.

AU - Butts, Craig

AU - Willis, Christine L.

PY - 2009

Y1 - 2009

N2 - Victorins are cyclic pentapeptide natural products isolated from the fungus Cochliobus victoriae. Using a combination of synthesis and spectroscopic methods we have assigned the geometry of the vinyl chloride residue and determined the stereochemistry of the 5,5-dichloroleucine moiety.

AB - Victorins are cyclic pentapeptide natural products isolated from the fungus Cochliobus victoriae. Using a combination of synthesis and spectroscopic methods we have assigned the geometry of the vinyl chloride residue and determined the stereochemistry of the 5,5-dichloroleucine moiety.

KW - Amino acids

KW - Halogenation

KW - Natural products

KW - Spectroscopy

KW - Stereoselective synthesis

UR - http://www.scopus.com/inward/record.url?scp=70449369121&partnerID=8YFLogxK

U2 - 10.1055/s-0029-1216910

DO - 10.1055/s-0029-1216910

M3 - Article (Academic Journal)

AN - SCOPUS:70449369121

SN - 0039-7881

SP - 2954

EP - 2962

JO - Synthesis (Germany)

JF - Synthesis (Germany)

IS - 17

ER -

Stereochemical assignments of the chlorinated residues in victorin C

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