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321 related items for PubMed ID: 22415756
1. Total synthesis of exiguamines A and B inspired by catecholamine chemistry. Sofiyev V, Lumb JP, Volgraf M, Trauner D. Chemistry; 2012 Apr 16; 18(16):4999-5005. PubMed ID: 22415756 [Abstract] [Full Text] [Related]
2. Biomimetic synthesis of the IDO inhibitors exiguamine A and B. Volgraf M, Lumb JP, Brastianos HC, Carr G, Chung MK, Münzel M, Mauk AG, Andersen RJ, Trauner D. Nat Chem Biol; 2008 Sep 16; 4(9):535-7. PubMed ID: 18677305 [Abstract] [Full Text] [Related]
3. Synthesis of indoleamine 2,3-dioxygenase inhibitory analogues of the sponge alkaloid exiguamine A. Carr G, Chung MK, Mauk AG, Andersen RJ. J Med Chem; 2008 May 08; 51(9):2634-7. PubMed ID: 18393489 [Abstract] [Full Text] [Related]
4. Total synthesis of (-)-herbindoles A, B, and C via transition-metal-catalyzed intramolecular [2 + 2 + 2] cyclization between ynamide and diynes. Saito N, Ichimaru T, Sato Y. Org Lett; 2012 Apr 06; 14(7):1914-7. PubMed ID: 22452396 [Abstract] [Full Text] [Related]
5. Unified Approach to the Spiro(pyrrolidinyl-oxindole) and Hexahydropyrrolo[2,3-b]indole Alkaloids: Total Syntheses of Pseudophrynamines 270 and 272A. De S, Das MK, Bhunia S, Bisai A. Org Lett; 2015 Dec 04; 17(23):5922-5. PubMed ID: 26600374 [Abstract] [Full Text] [Related]
6. Evolution of a synthetic strategy: total synthesis of (+/-)-welwitindolinone A isonitrile. Reisman SE, Ready JM, Weiss MM, Hasuoka A, Hirata M, Tamaki K, Ovaska TV, Smith CJ, Wood JL. J Am Chem Soc; 2008 Feb 13; 130(6):2087-100. PubMed ID: 18198870 [Abstract] [Full Text] [Related]
7. A flexible, convergent approach to polycyclic indole structures: formal synthesis of (+/-)-mersicarpine. Biechy A, Zard SZ. Org Lett; 2009 Jul 02; 11(13):2800-3. PubMed ID: 19489601 [Abstract] [Full Text] [Related]
8. Exiguamine A, an indoleamine-2,3-dioxygenase (IDO) inhibitor isolated from the marine sponge Neopetrosia exigua. Brastianos HC, Vottero E, Patrick BO, Van Soest R, Matainaho T, Mauk AG, Andersen RJ. J Am Chem Soc; 2006 Dec 20; 128(50):16046-7. PubMed ID: 17165752 [Abstract] [Full Text] [Related]
10. An organocatalytic [3+2] cyclisation strategy for the highly enantioselective synthesis of spirooxindoles. Voituriez A, Pinto N, Neel M, Retailleau P, Marinetti A. Chemistry; 2010 Nov 08; 16(42):12541-4. PubMed ID: 20853298 [No Abstract] [Full Text] [Related]
12. Total synthesis of spirobacillene A. Unsworth WP, Cuthbertson JD, Taylor RJ. Org Lett; 2013 Jul 05; 15(13):3306-9. PubMed ID: 23786419 [Abstract] [Full Text] [Related]
13. Total synthesis of (-)-ardeemin. He B, Song H, Du Y, Qin Y. J Org Chem; 2009 Jan 02; 74(1):298-304. PubMed ID: 19007134 [Abstract] [Full Text] [Related]
17. General access to the vinca and tacaman alkaloids using a Rh(II)-catalyzed cyclization/cycloaddition cascade. England DB, Padwa A. J Org Chem; 2008 Apr 04; 73(7):2792-802. PubMed ID: 18318547 [Abstract] [Full Text] [Related]
18. An organocatalytic Mannich/denitration reaction for the asymmetric synthesis of 3-ethylacetate-substitued 3-amino-2-oxindoles: formal synthesis of AG-041R. Zhao K, Shu T, Jia J, Raabe G, Enders D. Chemistry; 2015 Mar 02; 21(10):3933-6. PubMed ID: 25630891 [Abstract] [Full Text] [Related]
20. Total synthesis of (±)-decursivine and (±)-serotobenine: a Witkop photocyclization/elimination/O-Michael addition cascade approach. Qin H, Xu Z, Cui Y, Jia Y. Angew Chem Int Ed Engl; 2011 May 02; 50(19):4447-9. PubMed ID: 21504033 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]