Synthesis of the β-hydroxydopa-γ-hydroxy-δ- sulfinylnorvaline component of ustiloxins a and B

Luke Hunter; Malcolm D. McLeod; Craig A. Hutton

doi:10.1039/b418876d

Synthesis of the β-hydroxydopa-γ-hydroxy-δ- sulfinylnorvaline component of ustiloxins a and B

Luke Hunter, Malcolm D. McLeod, Craig A. Hutton^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

8 Citations (Scopus)

Abstract

The dopa-sulfinylnorvaline component of ustiloxins A and B has been prepared using an Evans salen-Al-catalysed aldol reaction with a 6-mercaptoisovanillin derivative, followed by incorporation of the norvaline group and asymmetric oxidation of the resulting sulfide to give the corresponding sulfoxide.

Original language	English
Pages (from-to)	732-734
Number of pages	3
Journal	Organic and Biomolecular Chemistry
Volume	3
Issue number	5
DOIs	https://doi.org/10.1039/b418876d
Publication status	Published - 7 Mar 2005
Externally published	Yes

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title = "Synthesis of the β-hydroxydopa-γ-hydroxy-δ- sulfinylnorvaline component of ustiloxins a and B",

abstract = "The dopa-sulfinylnorvaline component of ustiloxins A and B has been prepared using an Evans salen-Al-catalysed aldol reaction with a 6-mercaptoisovanillin derivative, followed by incorporation of the norvaline group and asymmetric oxidation of the resulting sulfide to give the corresponding sulfoxide.",

author = "Luke Hunter and McLeod, \{Malcolm D.\} and Hutton, \{Craig A.\}",

year = "2005",

month = mar,

day = "7",

doi = "10.1039/b418876d",

language = "English",

volume = "3",

pages = "732--734",

journal = "Organic and Biomolecular Chemistry",

issn = "1477-0520",

publisher = "Royal Society of Chemistry",

number = "5",

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T1 - Synthesis of the β-hydroxydopa-γ-hydroxy-δ- sulfinylnorvaline component of ustiloxins a and B

AU - Hunter, Luke

AU - McLeod, Malcolm D.

AU - Hutton, Craig A.

PY - 2005/3/7

Y1 - 2005/3/7

N2 - The dopa-sulfinylnorvaline component of ustiloxins A and B has been prepared using an Evans salen-Al-catalysed aldol reaction with a 6-mercaptoisovanillin derivative, followed by incorporation of the norvaline group and asymmetric oxidation of the resulting sulfide to give the corresponding sulfoxide.

AB - The dopa-sulfinylnorvaline component of ustiloxins A and B has been prepared using an Evans salen-Al-catalysed aldol reaction with a 6-mercaptoisovanillin derivative, followed by incorporation of the norvaline group and asymmetric oxidation of the resulting sulfide to give the corresponding sulfoxide.

UR - https://www.scopus.com/pages/publications/15244350598

U2 - 10.1039/b418876d

DO - 10.1039/b418876d

M3 - Article

SN - 1477-0520

VL - 3

SP - 732

EP - 734

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

IS - 5

ER -

Synthesis of the β-hydroxydopa-γ-hydroxy-δ- sulfinylnorvaline component of ustiloxins a and B

Abstract

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