Acetoxylation of β-lactams with lead(IV) acetate

Le Thanh Giang; József Fetter; Mária Kajtár-Peredy; Károly Lempert; Gábor Czira

doi:10.1016/S0040-4020(99)00857-1

Acetoxylation of β-lactams with lead(IV) acetate

Le Thanh Giang, József Fetter, Mária Kajtár-Peredy, Károly Lempert, Gábor Czira

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

2 Citations (Scopus)

Abstract

1-(4-Methoxyphenyl)azetidin-2-ones 5a-5g were acetoxylated by lead(IV) acetate to afford the corresponding compounds 6a, 6b, 6c' and 6d-6g. In the d series elimination products 9 and 10 were also formed. Ring homologue 7a afforded the hydroxylated derivative 8'a.

Original language	English
Pages (from-to)	13741-13748
Number of pages	8
Journal	Tetrahedron
Volume	55
Issue number	48
DOIs	https://doi.org/10.1016/S0040-4020(99)00857-1
Publication status	Published - 26 Nov 1999
Externally published	Yes

Keywords

Azetidin-2-ones
Oxidative Acetoxylation
Pyrrolidin-2-ones

Access to Document

10.1016/S0040-4020(99)00857-1

Cite this

@article{2bd599e88614430b9623f5cde939fa6d,

title = "Acetoxylation of β-lactams with lead(IV) acetate",

abstract = "1-(4-Methoxyphenyl)azetidin-2-ones 5a-5g were acetoxylated by lead(IV) acetate to afford the corresponding compounds 6a, 6b, 6c' and 6d-6g. In the d series elimination products 9 and 10 were also formed. Ring homologue 7a afforded the hydroxylated derivative 8'a.",

keywords = "Azetidin-2-ones, Oxidative Acetoxylation, Pyrrolidin-2-ones",

author = "Giang, {Le Thanh} and J{\'o}zsef Fetter and M{\'a}ria Kajt{\'a}r-Peredy and K{\'a}roly Lempert and G{\'a}bor Czira",

year = "1999",

month = nov,

day = "26",

doi = "10.1016/S0040-4020(99)00857-1",

language = "English",

volume = "55",

pages = "13741--13748",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier",

number = "48",

}

TY - JOUR

T1 - Acetoxylation of β-lactams with lead(IV) acetate

AU - Giang, Le Thanh

AU - Fetter, József

AU - Kajtár-Peredy, Mária

AU - Lempert, Károly

AU - Czira, Gábor

PY - 1999/11/26

Y1 - 1999/11/26

N2 - 1-(4-Methoxyphenyl)azetidin-2-ones 5a-5g were acetoxylated by lead(IV) acetate to afford the corresponding compounds 6a, 6b, 6c' and 6d-6g. In the d series elimination products 9 and 10 were also formed. Ring homologue 7a afforded the hydroxylated derivative 8'a.

AB - 1-(4-Methoxyphenyl)azetidin-2-ones 5a-5g were acetoxylated by lead(IV) acetate to afford the corresponding compounds 6a, 6b, 6c' and 6d-6g. In the d series elimination products 9 and 10 were also formed. Ring homologue 7a afforded the hydroxylated derivative 8'a.

KW - Azetidin-2-ones

KW - Oxidative Acetoxylation

KW - Pyrrolidin-2-ones

UR - http://www.scopus.com/inward/record.url?scp=0033607799&partnerID=8YFLogxK

U2 - 10.1016/S0040-4020(99)00857-1

DO - 10.1016/S0040-4020(99)00857-1

M3 - Article

AN - SCOPUS:0033607799

VL - 55

SP - 13741

EP - 13748

JO - Tetrahedron

JF - Tetrahedron

SN - 0040-4020

IS - 48

ER -

Acetoxylation of β-lactams with lead(IV) acetate

Abstract

Keywords

Access to Document

Other files and links

Cite this