Synthesis of 2,3-benzo-fused 1-oxacephems

Malcolm M Campbell; Kenneth H Nelson; A. Forbes Cameron

doi:10.1039/C39790000532

Synthesis of 2,3-benzo-fused 1-oxacephems

Malcolm M Campbell, Kenneth H Nelson, A. Forbes Cameron

School of Engineering & Physical Sciences

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

13 Citations (Scopus)

Abstract

4-Acetoxyazetidin-2-one (2) reacted with salicylaldehyde and 2-hydroxyphenyl ketones to give tricyclic hydroxy-amine products, and the reaction with ethyl 2-hydroxyphenylacetate was employed in the synthesis of a 2,3-benzo-fused ethoxycarbonyl 1-oxa analogue of the cephems.

Original language	English
Pages (from-to)	532-533
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	12
DOIs	https://doi.org/10.1039/C39790000532
Publication status	Published - 1979

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title = "Synthesis of 2,3-benzo-fused 1-oxacephems",

abstract = "4-Acetoxyazetidin-2-one (2) reacted with salicylaldehyde and 2-hydroxyphenyl ketones to give tricyclic hydroxy-amine products, and the reaction with ethyl 2-hydroxyphenylacetate was employed in the synthesis of a 2,3-benzo-fused ethoxycarbonyl 1-oxa analogue of the cephems.",

author = "Campbell, {Malcolm M} and Nelson, {Kenneth H} and Cameron, {A. Forbes}",

year = "1979",

doi = "10.1039/C39790000532",

language = "English",

pages = "532--533",

journal = "Journal of the Chemical Society, Chemical Communications",

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number = "12",

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T1 - Synthesis of 2,3-benzo-fused 1-oxacephems

AU - Campbell, Malcolm M

AU - Nelson, Kenneth H

AU - Cameron, A. Forbes

PY - 1979

Y1 - 1979

N2 - 4-Acetoxyazetidin-2-one (2) reacted with salicylaldehyde and 2-hydroxyphenyl ketones to give tricyclic hydroxy-amine products, and the reaction with ethyl 2-hydroxyphenylacetate was employed in the synthesis of a 2,3-benzo-fused ethoxycarbonyl 1-oxa analogue of the cephems.

AB - 4-Acetoxyazetidin-2-one (2) reacted with salicylaldehyde and 2-hydroxyphenyl ketones to give tricyclic hydroxy-amine products, and the reaction with ethyl 2-hydroxyphenylacetate was employed in the synthesis of a 2,3-benzo-fused ethoxycarbonyl 1-oxa analogue of the cephems.

UR - http://www.scopus.com/inward/record.url?scp=37049106577&partnerID=8YFLogxK

U2 - 10.1039/C39790000532

DO - 10.1039/C39790000532

M3 - Article

SN - 0022-4936

SP - 532

EP - 533

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

IS - 12

ER -

Synthesis of 2,3-benzo-fused 1-oxacephems

Abstract

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