Tamaru S - Search Results

1

A tin-complexation strategy for use with diverse acylation methods in the preparation of 1,9-diacyldipyrromethanes.

Tamaru S, Yu L, Youngblood WJ, Muthukumaran K, Taniguchi M, Lindsey JS. Tamaru S, et al. J Org Chem. 2004 Feb 6;69(3):765-77. doi: 10.1021/jo035622s. J Org Chem. 2004. PMID: 14750803

2

Porphyrins bearing arylphosphonic acid tethers for attachment to oxide surfaces.

Muthukumaran K, Loewe RS, Ambroise A, Tamaru S, Li Q, Mathur G, Bocian DF, Misra V, Lindsey JS. Muthukumaran K, et al. Among authors: tamaru s. J Org Chem. 2004 Mar 5;69(5):1444-52. doi: 10.1021/jo034945l. J Org Chem. 2004. PMID: 14986995

3

9-Acylation of 1-acyldipyrromethanes containing a dialkylboron mask for the alpha-acylpyrrole motif.

Zaidi SH, Muthukumaran K, Tamaru S, Lindsey JS. Zaidi SH, et al. Among authors: tamaru s. J Org Chem. 2004 Nov 26;69(24):8356-65. doi: 10.1021/jo048587d. J Org Chem. 2004. PMID: 15549807

4

A pH-responsive carboxylic β-1,3-glucan polysaccharide for complexation with polymeric guests.

Lien le TN, Shiraki T, Dawn A, Tsuchiya Y, Tokunaga D, Tamaru S, Enomoto N, Hojo J, Shinkai S. Lien le TN, et al. Among authors: tamaru s. Org Biomol Chem. 2011 Jun 7;9(11):4266-75. doi: 10.1039/c1ob05114h. Epub 2011 Apr 11. Org Biomol Chem. 2011. PMID: 21483941

5

Studies on a new class of organogelator containing 2-anthracenecarboxylic acid: influence of gelator and solvent on stereochemistry of the photodimers.

Dawn A, Fujita N, Haraguchi S, Sada K, Tamaru S, Shinkai S. Dawn A, et al. Among authors: tamaru s. Org Biomol Chem. 2009 Nov 7;7(21):4378-85. doi: 10.1039/b910741j. Epub 2009 Aug 26. Org Biomol Chem. 2009. PMID: 19830286

6

Rational design of a sugar-appended porphyrin gelator that is forced to assemble into a one-dimensional aggregate.

Tamaru S, Nakamura M, Takeuchi M, Shinkai S. Tamaru S, et al. Org Lett. 2001 Nov 15;3(23):3631-4. doi: 10.1021/ol0165544. Org Lett. 2001. PMID: 11700099

7

Sol-gel polycondensation of tetraethyl orthosilicate (TEOS) in sugar-based porphyrin organogels: inorganic conversion of a sugar-directed porphyrinic fiber library through sol-gel transcription processes.

Kawano S, Tamaru S, Fujita N, Shinkai S. Kawano S, et al. Among authors: tamaru s. Chemistry. 2004 Jan 23;10(2):343-51. doi: 10.1002/chem.200305042. Chemistry. 2004. PMID: 14735502

8

What kind of "soft materials" can we design from molecular gels?

Dawn A, Shiraki T, Haraguchi S, Tamaru S, Shinkai S. Dawn A, et al. Among authors: tamaru s. Chem Asian J. 2011 Feb 1;6(2):266-82. doi: 10.1002/asia.201000217. Epub 2010 Aug 16. Chem Asian J. 2011. PMID: 20715040

9

Giant amino acids designed on the polysaccharide scaffold and their protein-like structural interconversion.

Tamaru S, Tokunaga D, Hori K, Matsuda S, Shinkai S. Tamaru S, et al. Org Biomol Chem. 2014 Feb 7;12(5):815-22. doi: 10.1039/c3ob41845f. Epub 2013 Dec 9. Org Biomol Chem. 2014. PMID: 24317299

10

Double helical silica fibrils by sol-gel transcription of chiral aggregates of gemini surfactants.

Sugiyasu K, Tamaru S, Takeuchi M, Berthier D, Huc I, Oda R, Shinkai S. Sugiyasu K, et al. Among authors: tamaru s. Chem Commun (Camb). 2002 Jun 7;(11):1212-3. doi: 10.1039/b202799m. Chem Commun (Camb). 2002. PMID: 12109087

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