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Synthesis of an isomer of the oxaspirobicyclic tetronic acid unit of the CCK-B receptor antagonist tetronothiodin
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作者:

Page, PCB
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机构:
Univ Loughborough, Dept Chem, Loughborough LE11 3TU, Leics, England Univ Loughborough, Dept Chem, Loughborough LE11 3TU, Leics, England

Vahedi, H
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机构: Univ Loughborough, Dept Chem, Loughborough LE11 3TU, Leics, England

Batchelor, KJ
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机构: Univ Loughborough, Dept Chem, Loughborough LE11 3TU, Leics, England

Hindley, SJ
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机构: Univ Loughborough, Dept Chem, Loughborough LE11 3TU, Leics, England

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Beswick, P
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机构: Univ Loughborough, Dept Chem, Loughborough LE11 3TU, Leics, England
机构:
[1] Univ Loughborough, Dept Chem, Loughborough LE11 3TU, Leics, England
[2] GlaxoSmithKline, Med Res Ctr, Dept Med Chem, Neurol & GI Ctr Excellence Drug Discovery, Stevenage SG2 2NY, Herts, England
来源:
关键词:
tetronothiodin;
Diels-Alder;
Dieckmann;
spiro tetronic acid;
CCK;
D O I:
10.1055/s-2003-39287
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
An isomer of the oxaspirobicyclic tetronic acid unit of the CCK-B Receptor antagonist tetronothiodin, diastereoisomeric at the spiro centre, has been synthesized in five steps from dienol 4.
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页码:1022 / 1024
页数:3
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