Synthesis of the β-lactone esterase inhibitor valilactone using π-allyltricarbonyliron lactone complexes.

Roderick W. Bates; Rosalina Fernández-Moro; Steven V. Ley

doi:10.1016/S0040-4039(00)78809-5

Synthesis of the β-lactone esterase inhibitor valilactone using π-allyltricarbonyliron lactone complexes.

Roderick W. Bates^*, Rosalina Fernández-Moro, Steven V. Ley

^*Corresponding author for this work

Imperial College London

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

33 Citations (Scopus)

Abstract

Synthesis of the esterase inhibitor valilactone (1) is reported employing the oxidation of π-allyltricarbonyliron lactone complexes with ceric ammonium nitrate to afford the inherent β-lactone ring.

Original language	English
Pages (from-to)	2651-2654
Number of pages	4
Journal	Tetrahedron Letters
Volume	32
Issue number	23
DOIs	https://doi.org/10.1016/S0040-4039(00)78809-5
Publication status	Published - Jun 3 1991
Externally published	Yes

ASJC Scopus Subject Areas

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4039(00)78809-5

Cite this

@article{4cb4603db99741299a0ea5680f38bc62,

title = "Synthesis of the β-lactone esterase inhibitor valilactone using π-allyltricarbonyliron lactone complexes.",

abstract = "Synthesis of the esterase inhibitor valilactone (1) is reported employing the oxidation of π-allyltricarbonyliron lactone complexes with ceric ammonium nitrate to afford the inherent β-lactone ring.",

author = "Bates, {Roderick W.} and Rosalina Fern{\'a}ndez-Moro and Ley, {Steven V.}",

year = "1991",

month = jun,

day = "3",

doi = "10.1016/S0040-4039(00)78809-5",

language = "English",

volume = "32",

pages = "2651--2654",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "23",

}

TY - JOUR

T1 - Synthesis of the β-lactone esterase inhibitor valilactone using π-allyltricarbonyliron lactone complexes.

AU - Bates, Roderick W.

AU - Fernández-Moro, Rosalina

AU - Ley, Steven V.

PY - 1991/6/3

Y1 - 1991/6/3

N2 - Synthesis of the esterase inhibitor valilactone (1) is reported employing the oxidation of π-allyltricarbonyliron lactone complexes with ceric ammonium nitrate to afford the inherent β-lactone ring.

AB - Synthesis of the esterase inhibitor valilactone (1) is reported employing the oxidation of π-allyltricarbonyliron lactone complexes with ceric ammonium nitrate to afford the inherent β-lactone ring.

UR - http://www.scopus.com/inward/record.url?scp=0025779797&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0025779797&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)78809-5

DO - 10.1016/S0040-4039(00)78809-5

M3 - Article

AN - SCOPUS:0025779797

SN - 0040-4039

VL - 32

SP - 2651

EP - 2654

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 23

ER -

Synthesis of the β-lactone esterase inhibitor valilactone using π-allyltricarbonyliron lactone complexes.

Abstract

ASJC Scopus Subject Areas

Access to Document

Other files and links

Fingerprint

Cite this