Flexible access to conformationally-locked bicyclic morpholines

Rachael Bogacki, Duncan M. Gill, W. J. Kerr, Scott Lamont, John A. Parkinson, Laura C. Paterson

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

A preparatively accessible route to a series of conformationally-locked bicyclic morpholines has been developed. This flexible approach allows for diversification in order for a small array of lead-like scaffolds to be synthesised from readily available key building blocks.
LanguageEnglish
Pages8931-8933
Number of pages3
JournalJournal of the Chemical Society, Chemical Communications
Volume49
Issue number79
Early online date15 Aug 2013
DOIs
Publication statusPublished - 10 Sep 2013

Fingerprint

Morpholines
Scaffolds
Lead

Keywords

  • flexible access
  • conformationally-locked
  • bicyclic morpholines

Cite this

Bogacki, Rachael ; Gill, Duncan M. ; Kerr, W. J. ; Lamont, Scott ; Parkinson, John A. ; Paterson, Laura C. / Flexible access to conformationally-locked bicyclic morpholines. In: Journal of the Chemical Society, Chemical Communications. 2013 ; Vol. 49, No. 79. pp. 8931-8933.
@article{389aa4986faa4c68b9d4893fd66eddbf,
title = "Flexible access to conformationally-locked bicyclic morpholines",
abstract = "A preparatively accessible route to a series of conformationally-locked bicyclic morpholines has been developed. This flexible approach allows for diversification in order for a small array of lead-like scaffolds to be synthesised from readily available key building blocks.",
keywords = "flexible access, conformationally-locked, bicyclic morpholines",
author = "Rachael Bogacki and Gill, {Duncan M.} and Kerr, {W. J.} and Scott Lamont and Parkinson, {John A.} and Paterson, {Laura C.}",
year = "2013",
month = "9",
day = "10",
doi = "10.1039/C3CC45627G",
language = "English",
volume = "49",
pages = "8931--8933",
journal = "Journal of the Chemical Society, Chemical Communications",
issn = "0022-4936",
number = "79",

}

Flexible access to conformationally-locked bicyclic morpholines. / Bogacki, Rachael; Gill, Duncan M.; Kerr, W. J.; Lamont, Scott; Parkinson, John A.; Paterson, Laura C.

In: Journal of the Chemical Society, Chemical Communications, Vol. 49, No. 79, 10.09.2013, p. 8931-8933.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Flexible access to conformationally-locked bicyclic morpholines

AU - Bogacki, Rachael

AU - Gill, Duncan M.

AU - Kerr, W. J.

AU - Lamont, Scott

AU - Parkinson, John A.

AU - Paterson, Laura C.

PY - 2013/9/10

Y1 - 2013/9/10

N2 - A preparatively accessible route to a series of conformationally-locked bicyclic morpholines has been developed. This flexible approach allows for diversification in order for a small array of lead-like scaffolds to be synthesised from readily available key building blocks.

AB - A preparatively accessible route to a series of conformationally-locked bicyclic morpholines has been developed. This flexible approach allows for diversification in order for a small array of lead-like scaffolds to be synthesised from readily available key building blocks.

KW - flexible access

KW - conformationally-locked

KW - bicyclic morpholines

UR - http://pubs.rsc.org/en/journals/journalissues/cc

U2 - 10.1039/C3CC45627G

DO - 10.1039/C3CC45627G

M3 - Article

VL - 49

SP - 8931

EP - 8933

JO - Journal of the Chemical Society, Chemical Communications

T2 - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

SN - 0022-4936

IS - 79

ER -