A new route to 6,6-disubstituted penams and 7,7-disubstituted cephems

Malcolm M Campbell; Graham Johnson

doi:10.1039/C39750000479

A new route to 6,6-disubstituted penams and 7,7-disubstituted cephems

Malcolm M Campbell
, Graham Johnson

School of Engineering & Physical Sciences

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

8 Citations (Scopus)

Abstract

The reaction of penicillanate esters with N-chloro-N-sodiourethane gave 6,6-diacylaminopenicillanates from which the corresponding 7,7- diacylaminodeacetoxycephalosporanates were prepared via the sulphoxides.

Original language	English
Pages (from-to)	479-480
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	12
DOIs	https://doi.org/10.1039/C39750000479
Publication status	Published - 1975

Access to Document

10.1039/C39750000479

Cite this

@article{d373a5be60d446e9b5ac9bf88eb81dcb,

title = "A new route to 6,6-disubstituted penams and 7,7-disubstituted cephems",

abstract = "The reaction of penicillanate esters with N-chloro-N-sodiourethane gave 6,6-diacylaminopenicillanates from which the corresponding 7,7- diacylaminodeacetoxycephalosporanates were prepared via the sulphoxides.",

author = "Campbell, \{Malcolm M\} and Graham Johnson",

year = "1975",

doi = "10.1039/C39750000479",

language = "English",

pages = "479--480",

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

issn = "0022-4936",

publisher = "Chemical Society",

number = "12",

}

TY - JOUR

T1 - A new route to 6,6-disubstituted penams and 7,7-disubstituted cephems

AU - Campbell, Malcolm M

AU - Johnson, Graham

PY - 1975

Y1 - 1975

N2 - The reaction of penicillanate esters with N-chloro-N-sodiourethane gave 6,6-diacylaminopenicillanates from which the corresponding 7,7- diacylaminodeacetoxycephalosporanates were prepared via the sulphoxides.

AB - The reaction of penicillanate esters with N-chloro-N-sodiourethane gave 6,6-diacylaminopenicillanates from which the corresponding 7,7- diacylaminodeacetoxycephalosporanates were prepared via the sulphoxides.

UR - https://www.scopus.com/pages/publications/17044411729

U2 - 10.1039/C39750000479

DO - 10.1039/C39750000479

M3 - Article

SN - 0022-4936

SP - 479

EP - 480

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

IS - 12

ER -

A new route to 6,6-disubstituted penams and 7,7-disubstituted cephems

Abstract

Access to Document

Other files and links

Fingerprint

Cite this