Synthetic, transformations of porphyrins - Advances 2002-2004

被引:53
作者
Senge, MO [1 ]
Richter, J [1 ]
机构
[1] Univ Potsdam, Inst Chem, D-14476 Golm, Germany
关键词
synthesis; chemical modification; functional group interconversions; C-C coupling reactions; review;
D O I
10.1142/S1088424604000313
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Contemporary methods for the modification of porphyrins are presented. In association with the Third International Conference on Porphyrins and Phthalocyanines (ICPP-3) a survey of current method developments and reactivity studies is made. The review focuses on synthetic transformations of porphyrins currently in use for various applications and on functional group transformations. A brief survey of important developments covers selectively the literature from late 2001 to early 2004. Copyright (c) 2004 Society of Porphyrins & Phthalocyanines.
引用
收藏
页码:934 / 953
页数:20
相关论文
共 211 条
[1]   Synthesis of β-thiophene-substituted 21,23-dithiaporphyrins [J].
Agarwal, N ;
Mishra, SP ;
Kumar, A ;
Ravikanth, M .
CHEMISTRY LETTERS, 2003, 32 (08) :744-745
[2]   Synthesis and crystal structure of 2,3,12,13-tetraalkoxy-21, 23-dithiaporphyrins [J].
Agarwal, N ;
Mishra, SP ;
Kumar, A ;
Hung, CH ;
Ravikanth, M .
CHEMICAL COMMUNICATIONS, 2002, (22) :2642-2643
[3]  
Aihara H, 2001, ANGEW CHEM INT EDIT, V40, P3439, DOI 10.1002/1521-3773(20010917)40:18<3439::AID-ANIE3439>3.0.CO
[4]  
2-Z
[5]   Hetero-Diels-Alder reactions of β-imino-meso-tetraphenylporphyrin derivatives:: a new approach to pyrido[2,3-b]porphyrins [J].
Alonso, CMA ;
Neves, MGPMS ;
Tomé, AC ;
Silva, AMS ;
Cavaleiro, JAS .
TETRAHEDRON LETTERS, 2001, 42 (47) :8307-8309
[6]   Synthesis of meso-meso linked hybrid porphyrin arrays by Pd-catalyzed cross-coupling reaction [J].
Aratani, N ;
Osuka, A .
ORGANIC LETTERS, 2001, 3 (26) :4213-4216
[7]   Syntheses of regioselectively functionalized, asymmetric porphyrins via "2+2" condensation [J].
Arumugam, N ;
Won, DH ;
Lee, CH .
JOURNAL OF PORPHYRINS AND PHTHALOCYANINES, 2002, 6 (7-8) :479-483
[8]   Tetrabiphenylporphyrin-based receptors for protein surfaces show sub-nanomolar affinity and enhance unfolding [J].
Aya, T ;
Hamilton, AD .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2003, 13 (16) :2651-2654
[9]   Controlling chirality and optical properties of artificial antenna systems with self-assembling porphyrins [J].
Balaban, TS ;
Bhise, AD ;
Fischer, M ;
Linke-Schaetzel, M ;
Roussel, C ;
Vanthuyne, N .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (19) :2140-2144
[10]   Iron polynitroporphyrins bearing up to eight β-nitro groups as interesting new catalysts for H2O2-dependent hydrocarbon oxidation:: unusual regioselectivity in hydroxylation of alkoxybenzenes [J].
Bartoli, JFO ;
Le Barch, K ;
Palacio, M ;
Battioni, P ;
Mansuy, D .
CHEMICAL COMMUNICATIONS, 2001, (18) :1718-1719