1,4-diacetoxy-β-lactams. Reactions with nucleophiles

P.A. van Elburg, David Reinhoudt, Sybolt Harkema, G.J. van Hummel

Research output: Contribution to journalArticleAcademic

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56 Downloads (Pure)

Abstract

β-Lactam reacts with hetero nucleophiles under ring cleavage to give 2,2-dimethyl-3-oximinobutanoic esters 6 and 7 . N-hydroxyazetidine 5 , the precursor of β-lactam 1, is prepared by a new method.
Original languageUndefined
Pages (from-to)2809-2812
JournalTetrahedron letters
Volume26
Issue number23
DOIs
Publication statusPublished - 1985

Keywords

  • IR-69457

Cite this

van Elburg, P.A. ; Reinhoudt, David ; Harkema, Sybolt ; van Hummel, G.J. / 1,4-diacetoxy-β-lactams. Reactions with nucleophiles. In: Tetrahedron letters. 1985 ; Vol. 26, No. 23. pp. 2809-2812.
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volume = "26",
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journal = "Tetrahedron letters",
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1,4-diacetoxy-β-lactams. Reactions with nucleophiles. / van Elburg, P.A.; Reinhoudt, David; Harkema, Sybolt; van Hummel, G.J.

In: Tetrahedron letters, Vol. 26, No. 23, 1985, p. 2809-2812.

Research output: Contribution to journalArticleAcademic

TY - JOUR

T1 - 1,4-diacetoxy-β-lactams. Reactions with nucleophiles

AU - van Elburg, P.A.

AU - Reinhoudt, David

AU - Harkema, Sybolt

AU - van Hummel, G.J.

PY - 1985

Y1 - 1985

N2 - β-Lactam reacts with hetero nucleophiles under ring cleavage to give 2,2-dimethyl-3-oximinobutanoic esters 6 and 7 . N-hydroxyazetidine 5 , the precursor of β-lactam 1, is prepared by a new method.

AB - β-Lactam reacts with hetero nucleophiles under ring cleavage to give 2,2-dimethyl-3-oximinobutanoic esters 6 and 7 . N-hydroxyazetidine 5 , the precursor of β-lactam 1, is prepared by a new method.

KW - IR-69457

U2 - 10.1016/S0040-4039(00)94918-9

DO - 10.1016/S0040-4039(00)94918-9

M3 - Article

VL - 26

SP - 2809

EP - 2812

JO - Tetrahedron letters

JF - Tetrahedron letters

SN - 0040-4039

IS - 23

ER -