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9 research outputs found

A New Method for the Synthesis of Imidazolidinone- and Benzimidazolone-Containing [2.2]Cyclophanes

Author: Alcalde E.
Alcalde E.
Bodwell G.
Boekelheide V.
Bruhin J.
Burkhardt Wilke
Cram D. J.
Gray R.
Haley J. F.
Imidazole
Keisha K. Ellis
Kimbonguila A. M.
Mashraqui S. H.
Paracyclophane
Pischel I.
Pye P. J.
Steven T. Diver
Timko J. M.
Yuegang Zhang
Publication venue: 'American Chemical Society (ACS)'
Publication date
Field of study

Scaling-Up Ionic Liquid-Based Technologies: How Much Do We Care About Their Toxicity? Prima Facie Information on 1-Ethyl-3-Methylimidazolium Acetate

Identification of a Second Conserved Polybasic Domain in Septin 9 Involved in MicrotubuleeDependent Golgi Assembly

Author: A
A A Bridges
A Akil
A Casamayor
A Pagliuso
Ama Gassama-Diagne
B
B Bisel
Bruno Goud
C
C Pendaries
C Po�s
C S Weirich
C T�ngemo
Christian Poos
Cyntia Taveneau
D
Didier Samuel
E L Wu
E Nocodazole
E Peterson
E T Spiliotis
F Bard
F Pan
H J C Berendsen
Hcl Tris
Imidazole
Jinchao Yua
Juan Peng
K Chabin-Brion
K O Schink
K Song
M G Waugh
M G Waugh
M Sirajuddin
Mohyeddine Omrane
P D Adams
Po�s
R Das
R Nishihama
Raphaal Guurois
S Rivero
S5 Figure
S6 Figure
Sttphane Bressanelli
T Balla
T Vinogradova
Thibault Tubiana
V5/His
Waugh
Y Oh
Y Song
Y Tanaka-Takiguchi
Y Xiang
Publication venue: 'Elsevier BV'
Publication date: 01/01/2018
Field of study

The exocyclic amino group of adenine in PtII and PdII complexes: a critical comparison of the X-ray crystallographic structural data and gas phase calculations

Author: A Bergner
A Eastman
A report on a RuII complex containing a chelating neutral 9MeA ligand with an intact N6H2 group seems to be inconsistent with the shortness of the C6–N6 bond (1.315(12) Å) and rather points to a rare tautomer structure of 9MeA. An unambiguous assignment of the site of proton attachment is difficult on the basis of the X-ray data however: Shan N, Vickers SJ, Adams H, Ward MD, Thomas JA
A Sigel
A Szent-Györgyi
A Terzis
AAA Attia
ACG Hotze
AH Velders
AK Chandra
AK Vrkic
AMJ Fichtinger-Schepman
Amr A. A. Attia
B Longato
B Luisi
Bernhard Lippert
Béla Mihály
C Fonseca Guerra
C Fonseca Guerra
C Meiser
C Price
CG Berry
CJ Cramer
D Amantia
D Brackemeyer
D Xing
DC Cowles
DP Smith
E Sletten
EF Day
EY Bivián-Castro
F Schwarz
F Zamora
FM Albertí
FM Albertí
G Bandoli
G Schröder
G Trovó
GL Eichhorn
H Chifotides
H Sigel
H Zhao
HT Chifotides
J Arpalahti
J Arpalahti
J Arpalahti
J Sponer
J Sponer
J Sponer
J Sponer
J Viljanen
J Zheng
JHJ Hartog den
JP Charland
JP Charland
JR Webb
K Aoki
K Inagaki
K Yaminari
KV Catalan
L Clowney
LE Kapinos
M Atoji
M Cossi
M Dolg
M Fukuyo
M Garijo Añorbe
M Garijo Añorbe
M Kaupp
M Korth
M Noguera
M Roitzsch
M Roitzsch
M Schreiber
MD Reily
ME Kastner
ME Prater
MJ Clarke
MJ Olivier
MS Lüth
MS Lüth
N Russo
P Amo-Ochoa
P Amo-Ochoa
PA Dub
Pablo J. Sanz Miguel
R Beyerle-Pfnür
R Cini
R Stewart
R Wagner
R Weiß
Radu Silaghi-Dumitrescu
RB Martin
RF Whiting
RK McMullan
RK Prajapati
RM Izatt
S Ibánez
S Ibánez
S Khanna
S Korn
S Korn
S Mansy
S Torker
S Verma
T Mihály
T Ren
TAJ Haystead
The designation of E (Entgegen) and Z (Zusammen) isomers is justified given the high double bond character of C6–N6 and the priority numbers of the two metal ions. It is noted that this designation is also in use for complexes having a single metal at N6 only with respect to the imidazole part of adenine: Rodriguez-Bailey VM, Clarke MJ
Timea Mihály
TJ Kistenmacher
TJ Kistenmacher
TR Harkins
V Barone
W Saenger
WI Sundquist
X Zhu
Y Hisamatsu
Y Zhao
Y Zhao
Y Zhao
Publication venue: 'Springer Science and Business Media LLC'
Publication date
Field of study

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