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Items: 11

1.

Synthesis of dimeric ADP-ribose and its structure with human poly(ADP-ribose) glycohydrolase.

Lambrecht MJ, Brichacek M, Barkauskaite E, Ariza A, Ahel I, Hergenrother PJ.

J Am Chem Soc. 2015 Mar 18;137(10):3558-64. doi: 10.1021/ja512528p. Epub 2015 Mar 4.

PMID:
25706250
2.

Stapedial synkinesis causing change in hearing threshold with facial motion.

Brichacek MA, Brandt MG, Carey JP, Byrne PJ.

Otol Neurotol. 2013 Jun;34(4):762-5. doi: 10.1097/MAO.0b013e31827f1909.

PMID:
23370552
3.
4.

Efficient synthesis of thiopyrans using a sulfur-enabled anionic cascade.

Li F, Calabrese D, Brichacek M, Lin I, Njardarson JT.

Angew Chem Int Ed Engl. 2012 Feb 20;51(8):1938-41. doi: 10.1002/anie.201108261. Epub 2012 Jan 10. No abstract available.

PMID:
22234934
5.

Stereospecific ring expansion of chiral vinyl aziridines.

Brichacek M, Villalobos MN, Plichta A, Njardarson JT.

Org Lett. 2011 Mar 4;13(5):1110-3. doi: 10.1021/ol200263g. Epub 2011 Feb 10.

6.

Enhanced gene and siRNA delivery by polycation-modified mesoporous silica nanoparticles loaded with chloroquine.

Bhattarai SR, Muthuswamy E, Wani A, Brichacek M, CastaƱeda AL, Brock SL, Oupicky D.

Pharm Res. 2010 Dec;27(12):2556-68. doi: 10.1007/s11095-010-0245-0. Epub 2010 Aug 21.

7.

An efficient oxidative dearomatization-radical cyclization approach to symmetrically substituted bicyclic guttiferone natural products.

McGrath NA, Binner JR, Markopoulos G, Brichacek M, Njardarson JT.

Chem Commun (Camb). 2011 Jan 7;47(1):209-11. doi: 10.1039/c0cc01419b. Epub 2010 Jul 7.

8.

Stereoselective ring expansion of vinyl oxiranes: mechanistic insights and natural product total synthesis.

Brichacek M, Batory LA, Njardarson JT.

Angew Chem Int Ed Engl. 2010 Feb 22;49(9):1648-51. doi: 10.1002/anie.200906830. No abstract available.

PMID:
20135664
9.

Creative approaches towards the synthesis of 2,5-dihydro- furans, thiophenes, and pyrroles. One method does not fit all!

Brichacek M, Njardarson JT.

Org Biomol Chem. 2009 May 7;7(9):1761-70. doi: 10.1039/b900236g. Epub 2009 Mar 11.

PMID:
19590767
10.

An efficient substrate-controlled approach towards hypoestoxide, a member of a family of diterpenoid natural products with an inside-out [9.3.1]bicyclic core.

McGrath NA, Lee CA, Araki H, Brichacek M, Njardarson JT.

Angew Chem Int Ed Engl. 2008;47(49):9450-3. doi: 10.1002/anie.200804237. No abstract available.

PMID:
18979485
11.

Lewis acid catalyzed [1,3]-sigmatropic rearrangement of vinyl aziridines.

Brichacek M, Lee D, Njardarson JT.

Org Lett. 2008 Nov 6;10(21):5023-6. doi: 10.1021/ol802123e. Epub 2008 Oct 9.

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