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Items: 1 to 20 of 97

1.

Facile synthesis of meso-arylamino- and alkylaminosubporphyrins.

Kitano M, Hayashi SY, Tanaka T, Aratani N, Osuka A.

Chemistry. 2012 Jul 16;18(29):8929-33. doi: 10.1002/chem.201201256. Epub 2012 Jun 19.

PMID:
22715052
2.

meso-Aryl-substituted subporphyrins: synthesis, structures, and large substituent effects on their electronic properties.

Inokuma Y, Yoon ZS, Kim D, Osuka A.

J Am Chem Soc. 2007 Apr 18;129(15):4747-61. Epub 2007 Mar 24.

PMID:
17381092
3.

Peripheral hexabromination, hexaphenylation, and hexaethynylation of meso-aryl-substituted subporphyrins.

Tsurumaki E, Inokuma Y, Easwaramoorthi S, Lim JM, Kim D, Osuka A.

Chemistry. 2009;15(1):237-47. doi: 10.1002/chem.200801802.

PMID:
19058269
4.
5.

Probing the rotational dynamics of meso-(2-substituted)aryl substituents in A2B-type subporphyrins.

Yoshida K, Copley G, Mori H, Osuka A.

Chemistry. 2014 Aug 4;20(32):10065-72. doi: 10.1002/chem.201402778. Epub 2014 Jun 26.

PMID:
24976497
6.

Synthesis of peripherally nitrated, aminated, and arylaminated subporphyrins.

Tsurumaki E, Osuka A.

Chem Asian J. 2013 Dec;8(12):3042-50. doi: 10.1002/asia.201300869. Epub 2013 Aug 26.

PMID:
24039007
7.

Axial ligand exchange reactions of meso-aryl subporphyrins-axially fluoro-substituted subporphyrin and a mu-oxo dimer and trimer of subporphyrins.

Shimizu S, Matsuda A, Kobayashi N.

Inorg Chem. 2009 Aug 17;48(16):7885-90. doi: 10.1021/ic900880b.

PMID:
19618899
8.

Subporphyrins: emerging contracted porphyrins with aromatic 14pi-electronic systems and bowl-shaped structures: rational and unexpected synthetic routes.

Inokuma Y, Osuka A.

Dalton Trans. 2008 May 21;(19):2517-26. doi: 10.1039/b719808f. Epub 2008 Mar 4.

PMID:
18443691
9.

Nucleophilic aromatic substitution reactions of meso-bromosubporphyrin: synthesis of a thiopyrane-fused subporphyrin.

Shimizu D, Mori H, Kitano M, Cha WY, Oh J, Tanaka T, Kim D, Osuka A.

Chemistry. 2014 Dec 1;20(49):16194-202. doi: 10.1002/chem.201405110. Epub 2014 Oct 21.

PMID:
25336122
10.

The synthesis of, and characterization of the dynamic processes occurring in Pd(II) chelate complexes of 2-pyridyldiphenylphosphine.

Liu J, Jacob C, Sheridan KJ, Al-Mosule F, Heaton BT, Iggo JA, Matthews M, Pelletier J, Whyman R, Bickley JF, Steiner A.

Dalton Trans. 2010 Sep 14;39(34):7921-35. doi: 10.1039/b918162h. Epub 2010 Jul 26.

PMID:
20657926
11.

First synthesis of tetrapyrrolylporphyrin

Furuta H, Maeda H, Furuta T, Osuka A.

Org Lett. 2000 Jan 27;2(2):187-9.

PMID:
10814278
12.
13.
14.

Structural diversity in expanded porphyrins.

Misra R, Chandrashekar TK.

Acc Chem Res. 2008 Feb;41(2):265-79. doi: 10.1021/ar700091k. Epub 2008 Feb 19. Review.

PMID:
18281947
15.

Substituent-Induced Perturbation Symmetries and Distortions of meso-tert-Butylporphyrins.

Song XZ, Jentzen W, Jaquinod L, Khoury RG, Medforth CJ, Jia SL, Ma JG, Smith KM, Shelnutt JA.

Inorg Chem. 1998 May 4;37(9):2117-2128.

PMID:
11670364
16.

Synthetic routes to meso-patterned porphyrins.

Lindsey JS.

Acc Chem Res. 2010 Feb 16;43(2):300-11. doi: 10.1021/ar900212t.

PMID:
19863076
17.

Effect of meso-substituents on the osmium tetraoxide reaction and pinacol-pinacolone rearrangement of the corresponding vic-dihydroxyporphyrins.

Chen Y, Medforth CJ, Smith KM, Alderfer J, Dougherty TJ, Pandey RK.

J Org Chem. 2001 Jun 1;66(11):3930-9.

PMID:
11375017
18.

Synthesis of corroles bearing up to three different meso substituents.

Guilard R, Gryko DT, Canard G, Barbe JM, Koszarna B, Brandès S, Tasior M.

Org Lett. 2002 Dec 12;4(25):4491-4.

PMID:
12465920
19.

meso-(4-(N,N-dialkylamino)phenyl)-substituted subporphyrins: remarkably perturbed absorption spectra and enhanced fluorescence by intramolecular charge transfer interactions.

Inokuma Y, Easwaramoorthi S, Yoon ZS, Kim D, Osuka A.

J Am Chem Soc. 2008 Sep 17;130(37):12234-5. doi: 10.1021/ja804846v. Epub 2008 Aug 23.

PMID:
18720986
20.

Effect of five membered versus six membered meso-substituents on structure and electronic properties of Mg(II) porphyrins: a combined experimental and theoretical study.

Ghosh A, Mobin SM, Fröhlich R, Butcher RJ, Maity DK, Ravikanth M.

Inorg Chem. 2010 Sep 20;49(18):8287-97. doi: 10.1021/ic1008522.

PMID:
20726516
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