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Year | Number of Results |
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2001 | 3 |
2010 | 1 |
2011 | 1 |
2024 | 0 |
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Page 1
Evaluation of quinazoline analogues as glucocerebrosidase inhibitors with chaperone activity.
J Med Chem. 2011 Feb 24;54(4):1033-58. doi: 10.1021/jm1008902. Epub 2011 Jan 20.
J Med Chem. 2011.
PMID: 21250698
Free PMC article.
Evaluation of 2-thioxo-2,3,5,6,7,8-hexahydropyrimido[4,5-d]pyrimidin-4(1H)-one analogues as GAA activators.
Marugan JJ, Zheng W, Motabar O, Southall N, Goldin E, Sidransky E, Aungst RA, Liu K, Sadhukhan SK, Austin CP.
Marugan JJ, et al. Among authors: aungst ra.
Eur J Med Chem. 2010 May;45(5):1880-97. doi: 10.1016/j.ejmech.2010.01.027. Epub 2010 Feb 1.
Eur J Med Chem. 2010.
PMID: 20206419
Free PMC article.
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Synthesis of (Z)-2-acyl-2-enals via retrocycloadditions of 5-acyl-4-alkyl-4H-1,3-dioxins: application in the total synthesis of the cytotoxin (+/-)-euplotin A.
Aungst RA Jr, Funk RL.
Aungst RA Jr, et al.
J Am Chem Soc. 2001 Sep 26;123(38):9455-6. doi: 10.1021/ja011470b.
J Am Chem Soc. 2001.
PMID: 11562234
No abstract available.
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Total synthesis of the sesquiterpene (+/-)-illudin C via an intramolecular nitrile oxide cycloaddition.
Aungst RA Jr, Chan C, Funk RL.
Aungst RA Jr, et al.
Org Lett. 2001 Aug 9;3(16):2611-3. doi: 10.1021/ol016314o.
Org Lett. 2001.
PMID: 11483073
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Stereoselective preparation of (Z)-2-(trialkylsilyloxy)-2-alkenals by retrocycloaddition reactions of 4H-4-Alkyl-5-(trialkylsilyloxy)-1,3-dioxins. Useful reactants for Lewis acid catalyzed [4 + 3] cyclizations.
Aungst RA Jr, Funk RL.
Aungst RA Jr, et al.
Org Lett. 2001 Nov 1;3(22):3553-5. doi: 10.1021/ol016668f.
Org Lett. 2001.
PMID: 11678706
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