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

Organic & biomolecular chemistry

Dawn A, Fujita N, Haraguchi S, Sada K, Tamaru S, Shinkai S.
PMID: 19830286
Org Biomol Chem. 2009 Nov 07;7(21):4378-85. doi: 10.1039/b910741j. Epub 2009 Aug 26.

A new class of binary organogelator (G1, G2 and G3) based on 2-anthracenecarboxylic acid (2Ac), attached noncovalently with the gelator counterpart containing a 3,4,5-tris(n-dodecyloxy)benzoylamide backbone has been developed. Among the three gelators, two (G2 and G3) are chiral containing...

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Dawn A, Fujita N, Haraguchi S, et al. Studies on a new class of organogelator containing 2-anthracenecarboxylic acid: influence of gelator and solvent on stereochemistry of the photodimers. Org Biomol Chem. 2009;7(21):4378-85doi: 10.1039/b910741j.
Dawn, A., Fujita, N., Haraguchi, S., Sada, K., Tamaru, S., & Shinkai, S. (2009). Studies on a new class of organogelator containing 2-anthracenecarboxylic acid: influence of gelator and solvent on stereochemistry of the photodimers. Organic & biomolecular chemistry, 7(21), 4378-85. https://doi.org/10.1039/b910741j
Dawn, Arnab, et al. "Studies on a new class of organogelator containing 2-anthracenecarboxylic acid: influence of gelator and solvent on stereochemistry of the photodimers." Organic & biomolecular chemistry vol. 7,21 (2009): 4378-85. doi: https://doi.org/10.1039/b910741j
Dawn A, Fujita N, Haraguchi S, Sada K, Tamaru S, Shinkai S. Studies on a new class of organogelator containing 2-anthracenecarboxylic acid: influence of gelator and solvent on stereochemistry of the photodimers. Org Biomol Chem. 2009 Nov 07;7(21):4378-85. doi: 10.1039/b910741j. Epub 2009 Aug 26. PMID: 19830286.
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Synthesis of Unprotected 2-Arylglycines by Transamination of Arylglyoxylic Acids with 2-(2-Chlorophenyl)glycine.

The Journal of organic chemistry

Inada H, Shibuya M, Yamamoto Y.
PMID: 32790313
J Org Chem. 2020 Sep 04;85(17):11047-11059. doi: 10.1021/acs.joc.0c01302. Epub 2020 Aug 18.

The transamination of α-keto acids with 2-phenylglycine is an effective methodology for directly synthesizing unprotected α-amino acids. However, the synthesis of 2-arylglycines by transamination is problematic because the corresponding products, 2-arylglycines, transaminate the starting arylglyoxylic acids. Herein, we demonstrate...

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Inada H, Shibuya M, Yamamoto Y. Synthesis of Unprotected 2-Arylglycines by Transamination of Arylglyoxylic Acids with 2-(2-Chlorophenyl)glycine. J Org Chem. 2020;85(17):11047-11059doi: 10.1021/acs.joc.0c01302.
Inada, H., Shibuya, M., & Yamamoto, Y. (2020). Synthesis of Unprotected 2-Arylglycines by Transamination of Arylglyoxylic Acids with 2-(2-Chlorophenyl)glycine. The Journal of organic chemistry, 85(17), 11047-11059. https://doi.org/10.1021/acs.joc.0c01302
Inada, Haruki, et al. "Synthesis of Unprotected 2-Arylglycines by Transamination of Arylglyoxylic Acids with 2-(2-Chlorophenyl)glycine." The Journal of organic chemistry vol. 85,17 (2020): 11047-11059. doi: https://doi.org/10.1021/acs.joc.0c01302
Inada H, Shibuya M, Yamamoto Y. Synthesis of Unprotected 2-Arylglycines by Transamination of Arylglyoxylic Acids with 2-(2-Chlorophenyl)glycine. J Org Chem. 2020 Sep 04;85(17):11047-11059. doi: 10.1021/acs.joc.0c01302. Epub 2020 Aug 18. PMID: 32790313.
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Enantioselective synthesis of (R)-2-cubylglycine including unprecedented rhodium mediated C-H insertion of cubane.

Organic & biomolecular chemistry

Houston SD, Chalmers BA, Savage GP, Williams CM.
PMID: 30644962
Org Biomol Chem. 2019 Jan 31;17(5):1067-1070. doi: 10.1039/c8ob02959h.

The first enantioselective synthesis of (R)-2-cubylglycine, an analogue of (R)-2-phenylglycine in which the phenyl ring has been replaced by cubane, is disclosed. The key step was a telescoped Strecker reaction using (S)-2-amino-2-phenylethanol as a chiral auxiliary. Exploration of an...

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Houston SD, Chalmers BA, Savage GP, et al. Enantioselective synthesis of (R)-2-cubylglycine including unprecedented rhodium mediated C-H insertion of cubane. Org Biomol Chem. 2019;17(5):1067-1070doi: 10.1039/c8ob02959h.
Houston, S. D., Chalmers, B. A., Savage, G. P., & Williams, C. M. (2019). Enantioselective synthesis of (R)-2-cubylglycine including unprecedented rhodium mediated C-H insertion of cubane. Organic & biomolecular chemistry, 17(5), 1067-1070. https://doi.org/10.1039/c8ob02959h
Houston, Sevan D, et al. "Enantioselective synthesis of (R)-2-cubylglycine including unprecedented rhodium mediated C-H insertion of cubane." Organic & biomolecular chemistry vol. 17,5 (2019): 1067-1070. doi: https://doi.org/10.1039/c8ob02959h
Houston SD, Chalmers BA, Savage GP, Williams CM. Enantioselective synthesis of (R)-2-cubylglycine including unprecedented rhodium mediated C-H insertion of cubane. Org Biomol Chem. 2019 Jan 31;17(5):1067-1070. doi: 10.1039/c8ob02959h. PMID: 30644962.
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Showing 1 to 3 of 3 entries