Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Glenn C. Condie"'
Autor:
David StC. Black, Michelle F. Channon, Kylie A. Clayton, Glenn C. Condie, Jason B. Harper, Naresh Kumar, Karin Pchalek, Tutik Dwi Wahyuningsih
Publikováno v:
ARKIVOC, Vol 2006, Iss 7, Pp 67-75 (2006)
Externí odkaz:
https://doaj.org/article/7014fa860ed94506a0c5086da409a41e
Publikováno v:
Arkivoc. 2021:1-12
Publikováno v:
Arkivoc. 2020:176-184
Publikováno v:
Arkivoc. 2020:20-32
Autor:
Donald Craig, Naresh Kumar, Michelle F. Channon, Mohan M. Bhadbhade, David StC. Black, Glenn C. Condie
Publikováno v:
Arkivoc. 2020:117-144
Autor:
V. Martinovic, Mohan M. Bhadbhade, Naresh Kumar, Mahiuddin Alamgir, Glenn C. Condie, David StC. Black, J. Wood
Publikováno v:
HETEROCYCLES. 100:1371
4,6-Dimethoxy-2-substituted-benzimidazoles undergo formylation, acylation, nitration and bromination at C7. The 7-carbaldehydes can be reduced to the corresponding hydroxymethyl compounds. Benzimidazole-2-carbaldehydes can be prepared by oxidation of
Autor:
Naresh Kumar, David StC. Black, Paul K. Bowyer, Vesna Martinovic, Glenn C. Condie, Hayat Sholihin, Joanne Wood, Mahiuddin Alamgir
Publikováno v:
HETEROCYCLES. 100:1189
Reversible aqueous metathesis reactions for potential application in dynamic combinatorial chemistry
Publikováno v:
Tetrahedron Letters. 51:5064-5067
Solutions of heterocycles having an allyl sulfide unit and simple alkenes in 50% t -BuOH/H 2 O undergo reversible olefin metathesis reactions with the second generation Hoveyda–Grubbs catalyst. The choice of functional groups is limited by competit
Publikováno v:
Molecular Crystals and Liquid Crystals. 440:141-146
A range of secondary 2-amidophenylglyoxylamides self-assemble by intermolecular hydrogen bonding between the secondary amide proton and the 2-amidophenyl carbonyl oxygen atom.
Publikováno v:
Tetrahedron. 61:4989-5004
The reactivity of some 5,7-dimethoxyindoles with respect to electrophiles has been investigated. The favoured sites for reaction are C3 and C4 and regioselectivity can be controlled by the judicious arrangement of electron-withdrawing substituents. R