2,7-Diazabicyclo[2.2.1]heptanes: novel asymmetric access and controlled bridge-opening

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2,7-Diazabicyclo[2.2.1]heptanes : novel asymmetric access and controlled bridge-opening. / Peczkowski, Gary; Craven, Philip; Stead, Darren; Simpkins, Nigel.

In: Chemical Communications , Vol. 55, No. 29, 12.03.2019, p. 4214-4217.

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@article{ccda6c0aea1d4a51bd553498cf52e3f4,
title = "2,7-Diazabicyclo[2.2.1]heptanes: novel asymmetric access and controlled bridge-opening",
abstract = "Organocatalysed asymmetric Michael additions of substituted triketopiperazines to enones afford products in high yield and enantiomeric ratio (er). Further modification delivers products possessing natural product (NP) scaffolds including diazabicyclo[2.2.1]heptane, prolinamide and harmicine.",
author = "Gary Peczkowski and Philip Craven and Darren Stead and Nigel Simpkins",
year = "2019",
month = mar,
day = "12",
doi = "10.1039/c8cc10263e",
language = "English",
volume = "55",
pages = "4214--4217",
journal = "Chemical Communications ",
issn = "1359-7345",
publisher = "Royal Society of Chemistry",
number = "29",

}

RIS

TY - JOUR

T1 - 2,7-Diazabicyclo[2.2.1]heptanes

T2 - novel asymmetric access and controlled bridge-opening

AU - Peczkowski, Gary

AU - Craven, Philip

AU - Stead, Darren

AU - Simpkins, Nigel

PY - 2019/3/12

Y1 - 2019/3/12

N2 - Organocatalysed asymmetric Michael additions of substituted triketopiperazines to enones afford products in high yield and enantiomeric ratio (er). Further modification delivers products possessing natural product (NP) scaffolds including diazabicyclo[2.2.1]heptane, prolinamide and harmicine.

AB - Organocatalysed asymmetric Michael additions of substituted triketopiperazines to enones afford products in high yield and enantiomeric ratio (er). Further modification delivers products possessing natural product (NP) scaffolds including diazabicyclo[2.2.1]heptane, prolinamide and harmicine.

UR - http://www.scopus.com/inward/record.url?scp=85064058664&partnerID=8YFLogxK

U2 - 10.1039/c8cc10263e

DO - 10.1039/c8cc10263e

M3 - Article

C2 - 30895973

VL - 55

SP - 4214

EP - 4217

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 29

ER -