A Metal-mediated Diastereoselective Synthesis of Precursors to the Aphid Pigment Derivatives

R.G.F. Giles; C.A. Joll; M.V. Sargent; Matthew Tilbrook

doi:10.1016/0040-4039(96)01748-0

A Metal-mediated Diastereoselective Synthesis of Precursors to the Aphid Pigment Derivatives

R.G.F. Giles, C.A. Joll, M.V. Sargent, Matthew Tilbrook

Vice-Chancellery

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

2 Citations (Scopus)

Abstract

Chiral compounds 16 and 17, precursors to the aphid insect pigment derivatives, have been prepared in good to high yield, with complete control of the diastereoselectivity at the newly-created chiral centre C-1, through the use of metal phenolates derived from naphthol 3. Copyright (C) 1996 Published by Elsevier Science Ltd

Original language	English
Pages (from-to)	7851-7854
Journal	Tetrahedron Letters
Volume	37
Issue number	43
DOIs	https://doi.org/10.1016/0040-4039(96)01748-0
Publication status	Published - 1996

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title = "A Metal-mediated Diastereoselective Synthesis of Precursors to the Aphid Pigment Derivatives",

abstract = "Chiral compounds 16 and 17, precursors to the aphid insect pigment derivatives, have been prepared in good to high yield, with complete control of the diastereoselectivity at the newly-created chiral centre C-1, through the use of metal phenolates derived from naphthol 3. Copyright (C) 1996 Published by Elsevier Science Ltd",

author = "R.G.F. Giles and C.A. Joll and M.V. Sargent and Matthew Tilbrook",

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T1 - A Metal-mediated Diastereoselective Synthesis of Precursors to the Aphid Pigment Derivatives

AU - Giles, R.G.F.

AU - Joll, C.A.

AU - Sargent, M.V.

AU - Tilbrook, Matthew

PY - 1996

Y1 - 1996

N2 - Chiral compounds 16 and 17, precursors to the aphid insect pigment derivatives, have been prepared in good to high yield, with complete control of the diastereoselectivity at the newly-created chiral centre C-1, through the use of metal phenolates derived from naphthol 3. Copyright (C) 1996 Published by Elsevier Science Ltd

AB - Chiral compounds 16 and 17, precursors to the aphid insect pigment derivatives, have been prepared in good to high yield, with complete control of the diastereoselectivity at the newly-created chiral centre C-1, through the use of metal phenolates derived from naphthol 3. Copyright (C) 1996 Published by Elsevier Science Ltd

U2 - 10.1016/0040-4039(96)01748-0

DO - 10.1016/0040-4039(96)01748-0

M3 - Article

VL - 37

SP - 7851

EP - 7854

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 43

ER -

A Metal-mediated Diastereoselective Synthesis of Precursors to the Aphid Pigment Derivatives

Abstract

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