Biosynthetic origins of the large macrolide, oligomycin A

John D. Bu'Lock; Gareth A. Morris; Michelle K. Richards

Biosynthetic origins of the large macrolide, oligomycin A

John D. Bu'Lock, Gareth A. Morris, Michelle K. Richards

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

Abstract

The overall biosynthesis of the large macrolide oligomycin A from a sequence of acetate, propionate and butyrate units, demonstrated by the specific incorporation of [1-13C]-labelled precursors, is in accord with the known structure, and the indirect incorporations from propionate and butyrate are very low. © 1986.

Original language	English
Pages (from-to)	2917-2920
Number of pages	3
Journal	Tetrahedron Letters
Volume	27
Issue number	25
Publication status	Published - 1986

Cite this

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title = "Biosynthetic origins of the large macrolide, oligomycin A",

abstract = "The overall biosynthesis of the large macrolide oligomycin A from a sequence of acetate, propionate and butyrate units, demonstrated by the specific incorporation of [1-13C]-labelled precursors, is in accord with the known structure, and the indirect incorporations from propionate and butyrate are very low. {\textcopyright} 1986.",

author = "Bu'Lock, {John D.} and Morris, {Gareth A.} and Richards, {Michelle K.}",

year = "1986",

language = "English",

volume = "27",

pages = "2917--2920",

journal = "Tetrahedron Letters",

issn = "1873-3581",

publisher = "Elsevier BV",

number = "25",

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TY - JOUR

T1 - Biosynthetic origins of the large macrolide, oligomycin A

AU - Bu'Lock, John D.

AU - Morris, Gareth A.

AU - Richards, Michelle K.

PY - 1986

Y1 - 1986

N2 - The overall biosynthesis of the large macrolide oligomycin A from a sequence of acetate, propionate and butyrate units, demonstrated by the specific incorporation of [1-13C]-labelled precursors, is in accord with the known structure, and the indirect incorporations from propionate and butyrate are very low. © 1986.

AB - The overall biosynthesis of the large macrolide oligomycin A from a sequence of acetate, propionate and butyrate units, demonstrated by the specific incorporation of [1-13C]-labelled precursors, is in accord with the known structure, and the indirect incorporations from propionate and butyrate are very low. © 1986.

M3 - Article

SN - 1873-3581

VL - 27

SP - 2917

EP - 2920

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 25

ER -

Biosynthetic origins of the large macrolide, oligomycin A

Abstract

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