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Yusuf Hamied Department of Chemistry

 

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  • Currently displaying 21601 - 21620 of 29542 publications
Comparison of empirically derived ozone losses in the Arctic vortex -: art. no. 8264
NRP Harris, M Rex, F Goutail, BM Knudsen, GL Manney, R Muller, P von der Gathen
– Journal of Geophysical Research
(2002)
107,
sol 7-1-sol 7-11
Total Syntheses and Structures of Angular [6]- and [7]Phenylene: The First Helical Phenylenes (Heliphenes)
S Han, AD Bond, RL Disch, D Holmes, JM Schulman, SJ Teat, KPC Vollhardt, GD Whitener
– Angewandte Chemie International Edition
(2002)
41,
3223
Total Syntheses and Structures of Angular [6]‐ and [7]Phenylene: The First Helical Phenylenes (Heliphenes)
S Han, AD Bond, RL Disch, D Holmes, JM Schulman, SJ Teat, KPC Vollhardt, GD Whitener
– Angewandte Chemie
(2002)
114,
3357
Titelbild: Angew. Chem. 17/2002
S Han, AD Bond, RL Disch, D Holmes, JM Schulman, SJ Teat, KPC Vollhardt, GD Whitener
– Angewandte Chemie
(2002)
114,
3199
Total Syntheses of Angular [7]‐, [8]‐, and [9]Phenylene by Triple Cobalt‐Catalyzed Cycloisomerization: Remarkably Flexible Heliphenes
S Han, DR Anderson, AD Bond, HV Chu, RL Disch, D Holmes, JM Schulman, SJ Teat, KPC Vollhardt, GD Whitener
– Angewandte Chemie
(2002)
114,
3361
Cover Picture: Angew. Chem. Int. Ed. 17/2002
S Han, DR Anderson, AD Bond, HV Chu, RL Disch, D Holmes, JM Schulman, SJ Teat, KPC Vollhardt, GD Whitener
– Angewandte Chemie International Edition
(2002)
41,
3071
Total Syntheses of Angular [7]‐, [8]‐, and [9]Phenylene by Triple Cobalt‐Catalyzed Cycloisomerization: Remarkably Flexible Heliphenes
S Han, DR Anderson, AD Bond, HV Chu, RL Disch, D Holmes, JM Schulman, SJ Teat, KPC Vollhardt, GD Whitener
– Angewandte Chemie International Edition
(2002)
41,
3227
Influence of molecular organization of asymmetrically substituted porphyrins on their response to NO2 gas
JM Pedrosa, CM Dooling, TH Richardson, RK Hyde, CA Hunter, MT Martín, L Camacho
– Langmuir
(2002)
18,
7594
Solid-state 93Nb, 19F, and 113Cd nuclear magnetic resonance study of niobium oxyfluorides:: Characterization of local distortions and oxygen/fluorine ordering
LS Du, RW Schurko, N Kim, CP Grey
– The Journal of Physical Chemistry A
(2002)
106,
7876
Concurrent nucleophilic and general acid catalysis of the hydrolysis of a phosphate triester
N Asaad, AJ Kirby
– J CHEM SOC PERK T 2
(2002)
1708
Synthesis, Structure Revision, and Absolute Configuration of (+)-Didemniserinolipid B, a Serinol Marine Natural Product from a Tunicate Didemnum sp.
H Kiyota, DJ Dixon, CK Luscombe, S Hettstedt, SV Ley
– Org Lett
(2002)
4,
3223
Probing oxygen motion in disordered anionic conductors with O-17 and V-51 MAS NMR spectroscopy
N Kim, CP Grey
– Science
(2002)
297,
1317
Sodium 1-hydroxy­pyridine-2(1H)-thiol­ate dihydrate
AD Bond
– Acta Crystallographica Section E: Crystallographic Communications
(2002)
58,
m492
Long-range ordering of methylidyne on Pt{110}(1×2)
MA Petersen, DTP Watson, SJ Jenkins, DA King
– The Journal of Chemical Physics
(2002)
117,
3951
Studies in marine macrolide synthesis: stereocontrolled synthesis of a C21–C34 subunit of the aplyronines
I Paterson, SB Blakey, CJ Cowden
– Tetrahedron Letters
(2002)
43,
6005
Determination of the extent to which an S(E)2 ' reaction of a propargylsilane is anti
I Fleming, KLC Pang
– Tetrahedron Letters
(2002)
43,
5985
Electronic structure and chemical potentials of molecules in spc/e water.
RM Lynden-Bell, S Murdock
– ABSTR PAP AM CHEM S
(2002)
224,
U501
Fundamental aspects of heterogeneous enantioselective catalysis: Surface chemistry of methyl pyruvate and (S)-1-(1-naphthyl)ethylamine on Pt{111}.
FJ Williams, JM Bonello, RM Lambert
– ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2002)
224,
U418
The synthesis of salmeterol using solid supported reagents.
SV Ley, RN Bream
– ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2002)
224,
U115
Application of analytical constructs to the development of an indole safety-catch linker family for solid phase organic synthesis.
JJ Scicinski, MS Congreve, SV Ley
– ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2002)
224,
U175