-
1
-
-
85168356779
-
Photosynthetic Light-Harvesting Pigment-Protein Complexes: Toward Understanding How and Why Crystal structure of an integral membrane light-harvesting complex from photosynthetic bacteria
-
1995
-
Pullerits T. Sundström V. Photosynthetic Light-Harvesting Pigment-Protein Complexes: Toward Understanding How and Why Acc. Chem. Res. 1996 29 381 389 McDermott G. Prince S. M. Freer A. A. Hawthornwaite-Lawless A. M. Papiz M. Z. Cogdell R. J. Isaacs N. W. Crystal structure of an integral membrane light-harvesting complex from photosynthetic bacteria Nature 1995 374 517 521
-
(1996)
Nature
, vol.374
, pp. 517-521
-
-
Pullerits, T.1
Sundström, V.2
-
2
-
-
85168316501
-
-
I -Promoted meso- meso Block Oligomerization Chem. Eur. J. 2000 6 3254 3271 Vicente M. G. H., Jaquinod L., Smith K. M. Oligomeric porphyrin arrays Chem. Commun 1999 1771 1782
-
I-Promoted meso- meso Block Oligomerization Chem. Eur. J. 2000 6 3254 3271 Vicente M. G. H., Jaquinod L., Smith K. M. Oligomeric porphyrin arrays Chem. Commun 1999 1771 1782
-
-
-
-
3
-
-
85168333087
-
-
For an excellent review see: Chambron J-C., Heitz V., Sauvage J-P. Noncovalent multiporphyrin assemblies Porphyrin Handbook 1 42 vol. 6 2000 Kadish K. M., Smith K. M., Guilard R
-
For an excellent review see: Chambron J-C., Heitz V., Sauvage J-P. Noncovalent multiporphyrin assemblies Porphyrin Handbook 1 42 vol. 6 2000 Kadish K. M., Smith K. M., Guilard R.
-
-
-
-
4
-
-
0003069302
-
Preparation of New Porphyrin BLOCKs and their Application to the Synthesis of Spacer and Cavity Ribbon Structures
-
Warrener R. N. Johnston M. R. Gunter M. J. Preparation of New Porphyrin BLOCKs and their Application to the Synthesis of Spacer and Cavity Ribbon Structures Synlett 1998 593 595 10.1055/s-1998-3136
-
(1998)
Synlett
, pp. 593-595
-
-
Warrener, R.N.1
Johnston, M.R.2
Gunter, M.J.3
-
5
-
-
0032556743
-
Templated formation of multiporphyrin assemblies resembling a molecular universal joint
-
Johnston M. R. Gunter M. J. Warrener R. N. Templated formation of multiporphyrin assemblies resembling a molecular universal joint Chem. Commun. 1998 2739 2740 10.1039/a807339b
-
(1998)
Chem. Commun
, pp. 2739-2740
-
-
Johnston, M.R.1
Gunter, M.J.2
Warrener, R.N.3
-
6
-
-
0033546237
-
New Porphyrin 4π-Cycloaddition Reagents and their use in the Preparation of Porphyrin-(Rigid Spacer)-1,10-Phenanthrolines in which Geometric ‘Tuning’ of the Chromophores is a Feature
-
Warrener R. N. Schultz A. C. Johnston M. R. Gunter M. J. New Porphyrin 4π-Cycloaddition Reagents and their use in the Preparation of Porphyrin-(Rigid Spacer)-1,10-Phenanthrolines in which Geometric ‘Tuning’ of the Chromophores is a Feature J. Org. Chem. 1999 64 4218 4219 10.1021/jo982487o
-
(1999)
J. Org. Chem
, vol.64
, pp. 4218-4219
-
-
Warrener, R.N.1
Schultz, A.C.2
Johnston, M.R.3
Gunter, M.J.4
-
7
-
-
85168339866
-
A New Building BlOCK Technique Based on Cycloaddition Chemistry for the Regiospecific Linking of Alicyclic Sub-units as a Route to Large, Custom-Functionalised Structures A 1,3-Dipolar Cycloaddition Route to 7-Azanorbornanes: Application to the Synthesis of syn-Facial N-Bridged Polynorbornanes
-
1998
-
Warrener R. N. Schultz A. C. Butler D. N. Wang S. Mahadevan I. B. Russell R. A. A New Building BlOCK Technique Based on Cycloaddition Chemistry for the Regiospecific Linking of Alicyclic Sub-units as a Route to Large, Custom-Functionalised Structures Chem. Commun. 1997 1023 1024 Margetic D. Russell R. A. Sun G. Warrener R. N. A 1,3-Dipolar Cycloaddition Route to 7-Azanorbornanes: Application to the Synthesis of syn-Facial N-Bridged Polynorbornanes Synlett 1998 588 589
-
(1997)
Synlett
, pp. 588-589
-
-
Warrener, R.N.1
Schultz, A.C.2
Butler, D.N.3
Wang, S.4
Mahadevan, I.B.5
Russell, R.A.6
-
8
-
-
37049071262
-
Synthesis of Porphyrin-2,3,12,13- and –2,3,7,8- tetrones: Building Blocks for the Synthesis of Extended Porphyrin Arrays An Approach to Porphyrin-based Molecular Wires: Synthesis of a Bis(porphyrin)tetraone and its Conversion to a Linearly Conjugated Tetrakisporphyrin System
-
1991
-
Crossley M. J. Govenlock L. J. Prashar J. K. Synthesis of Porphyrin-2,3,12,13- and –2,3,7,8- tetrones: Building Blocks for the Synthesis of Extended Porphyrin Arrays J. Chem. Soc., Chem. Commun. 1995 2379 2380 Crossley M. J. Burn P. L. An Approach to Porphyrin-based Molecular Wires: Synthesis of a Bis(porphyrin)tetraone and its Conversion to a Linearly Conjugated Tetrakisporphyrin System J. Chem. Soc., Chem. Commun. 1991 1569 1571
-
(1995)
J. Chem. Soc., Chem. Commun
, pp. 1569-1571
-
-
Crossley, M.J.1
Govenlock, L.J.2
Prashar, J.K.3
-
10
-
-
0000364195
-
The synthesis of functionalised cavity structures via 1,3-dipolar cycloaddition of angle-shaped alkenes to curved norbornene framed dipoles
-
Warrener R. N. Margetic D. Amarasekara A. S. Russell R. A. The synthesis of functionalised cavity structures via 1,3-dipolar cycloaddition of angle-shaped alkenes to curved norbornene framed dipoles Org. Lett. 1999 2 203 206 10.1021/ol990538d
-
(1999)
Org. Lett
, vol.2
, pp. 203-206
-
-
Warrener, R.N.1
Margetic, D.2
Amarasekara, A.S.3
Russell, R.A.4
-
11
-
-
85168352300
-
Synthesis, Spectroscopic Properties and Transannular Interactions of Tricyclic 1,2-Cyclobutanediones Design and Synthesis of α-Diketones. The Cyclobutane-1,2-dione Chromophore: Synthesis, Dienophilic Reactivity and Electronic Properties of Cyclobutenedione and Polycyclic Cyclobutanediones
-
1985
-
Martin H-D. Schiwek H-J. Spanget-Larsen J. Gleiter R. Synthesis, Spectroscopic Properties and Transannular Interactions of Tricyclic 1,2-Cyclobutanediones Chem. Ber. 1978 111 2557 2562 Albert B. Heller C. Iden R. Martin G. Martin H-D. Mayer B. Oftring A. Design and Synthesis of α-Diketones. The Cyclobutane-1,2-dione Chromophore: Synthesis, Dienophilic Reactivity and Electronic Properties of Cyclobutenedione and Polycyclic Cyclobutanediones Israel J. Chem. 1985 25 74 83
-
(1978)
Israel J. Chem
, vol.25
, pp. 74-83
-
-
Martin, H.-D.1
Schiwek, H.-J.2
Spanget-Larsen, J.3
Gleiter, R.4
-
12
-
-
85168321693
-
-
2 workstation. Minimisations were done without peripheral substituents such as aromatic rings or ester groups which have no bearing on the geometric outcome of the calculation
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2workstation. Minimisations were done without peripheral substituents such as aromatic rings or ester groups which have no bearing on the geometric outcome of the calculation.
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-
-
-
14
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0035857266
-
syn-Facial hetero-bridged [n]polynorbornanes: a new class of polarofacial framework molecules composed of fused 7-oxa- and 7-azanorbornanes
-
-
Warrener R. N. Margetic D. M. Foley P. J. Butler D. N. Winling A. Beales K. A. Russell R. A. syn-Facial hetero-bridged [n]polynorbornanes: a new class of polarofacial framework molecules composed of fused 7-oxa- and 7-azanorbornanes Tetrahedron 2001 in press 10.1016/S0040-4020(00)01027-9
-
(2001)
Tetrahedron
-
-
Warrener, R.N.1
Margetic, D.M.2
Foley, P.J.3
Butler, D.N.4
Winling, A.5
Beales, K.6
Russell, R.A.7
-
15
-
-
0032537662
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Synthesis and Modelling of Novel Rigid Rods derived from a Simple pentacyclic bis-norbornene
-
Margetic D. Johnston M. R. Tiekink E. R. T. Warrener R. N. Synthesis and Modelling of Novel Rigid Rods derived from a Simple pentacyclic bis-norbornene Tetrahedron Lett. 1998 39 5277 5280 10.1016/S0040-4039(98)00999-X
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 5277-5280
-
-
Margetic, D.1
Johnston, M.R.2
Tiekink, E.R.T.3
Warrener, R.N.4
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