Bianca Rose Sculimbrene
Affiliations: | 2004 | Boston College, Newton, MA, United States |
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"Bianca Sculimbrene"Mean distance: 7.82 | S | N | B | C | P |
Parents
Sign in to add mentorEdward E. Fenlon | research assistant | 1997-1999 | Xavier University | |
Scott Joseph Miller | grad student | 2004 | Boston College | |
(Catalytic asymmetric phosphorylation: Concise total syntheses of inositol phosphates.) |
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Publications
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Ouellette ET, Lougee MG, Bucknam AR, et al. (2021) Desymmetrization of Diols by Phosphorylation with a Titanium-BINOLate Catalyst. The Journal of Organic Chemistry |
Shugrue CR, Sculimbrene BR, Jarvo ER, et al. (2019) Outer-Sphere Control for Divergent Multicatalysis with Common Catalytic Moieties. The Journal of Organic Chemistry |
Coppola KA, Testa JW, Allen EE, et al. (2014) Selective phosphorylation of diols with a Lewis acid catalyst Tetrahedron Letters. 55: 4203-4206 |
Poremba KE, Lee VA, Sculimbrene BR. (2014) Synthesis of α-chiral-β,γ-unsaturated carboxylic acid derivatives using chiral auxiliaries Tetrahedron. 5463-5467 |
Fenton OS, Allen EE, Pedretty KP, et al. (2012) Catalytic Lewis acid phosphorylation with pyrophosphates Tetrahedron. 68: 9023-9028 |
Quinn RK, Cianci AL, Beaudoin JA, et al. (2010) Synthesis of a D-Ala-D-Ala peptide isostere via olefin cross-metathesis and evaluation of vancomycin binding. Bioorganic & Medicinal Chemistry Letters. 20: 4382-5 |
Sculimbrene BR, Miller SJ. (2010) ChemInform Abstract: Discovery of a Catalytic Asymmetric Phosphorylation Through Selection of a Minimal Kinase Mimic: A Concise Total Synthesis of D-myo-Inositol-1-phosphate. Cheminform. 33: no-no |
Brady PB, Morris EM, Fenton OS, et al. (2009) Efficient catalyst turnover in the phosphitylation of alcohols with phosphoramidites Tetrahedron Letters. 50: 975-978 |
Reynolds AM, Sculimbrene BR, Imperiali B. (2008) Lanthanide-binding tags with unnatural amino acids: sensitizing Tb3+ and Eu3+ luminescence at longer wavelengths. Bioconjugate Chemistry. 19: 588-91 |
Xu Y, Sculimbrene BR, Miller SJ. (2006) Streamlined synthesis of phosphatidylinositol (PI), PI3P, PI3,5P2, and deoxygenated analogues as potential biological probes. The Journal of Organic Chemistry. 71: 4919-28 |