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Results: 1 to 20 of 230

1.

Synthesis of many different types of organic small molecules using one automated process.

Li J, Ballmer SG, Gillis EP, Fujii S, Schmidt MJ, Palazzolo AM, Lehmann JW, Morehouse GF, Burke MD.

Science. 2015 Mar 13;347(6227):1221-6. doi: 10.1126/science.aaa5414.

PMID:
25766227
2.

A meta-analysis of single-case research on behavior contracts: effects on behavioral and academic outcomes among children and youth.

Bowman-Perrott L, Burke MD, de Marin S, Zhang N, Davis H.

Behav Modif. 2015 Mar;39(2):247-69. doi: 10.1177/0145445514551383. Epub 2014 Sep 26.

PMID:
25261083
3.

Reading interventions for middle and secondary students with emotional and behavioral disorders: a quantitative review of single-case studies.

Burke MD, Boon RT, Hatton H, Bowman-Perrott L.

Behav Modif. 2015 Jan;39(1):43-68. doi: 10.1177/0145445514547958. Epub 2014 Aug 26.

PMID:
25164773
4.

Synthesis of most polyene natural product motifs using just 12 building blocks and one coupling reaction.

Woerly EM, Roy J, Burke MD.

Nat Chem. 2014 Jun;6(6):484-91. Erratum in: Nat Chem. 2014 Jun 20;6(7):650.

5.

Amphotericin forms an extramembranous and fungicidal sterol sponge.

Anderson TM, Clay MC, Cioffi AG, Diaz KA, Hisao GS, Tuttle MD, Nieuwkoop AJ, Comellas G, Maryum N, Wang S, Uno BE, Wildeman EL, Gonen T, Rienstra CM, Burke MD.

Nat Chem Biol. 2014 May;10(5):400-6. doi: 10.1038/nchembio.1496. Epub 2014 Mar 30.

6.

(1-bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis.

Woerly EM, Miller JE, Burke MD.

Tetrahedron. 2013 Sep 9;69(36). doi: 10.1016/j.tet.2013.05.050. No abstract available.

7.

C2'-OH of amphotericin B plays an important role in binding the primary sterol of human cells but not yeast cells.

Wilcock BC, Endo MM, Uno BE, Burke MD.

J Am Chem Soc. 2013 Jun 12;135(23):8488-91. doi: 10.1021/ja403255s. Epub 2013 Jun 3.

8.

Stability enhancement of drug layered pellets in a fixed dose combination tablet.

Burke MD, He X, Cook C, Petrov GA, Long S, Coffin MD.

AAPS PharmSciTech. 2013 Mar;14(1):312-20. doi: 10.1208/s12249-012-9911-3. Epub 2013 Jan 15.

9.

Electronic tuning of site-selectivity.

Wilcock BC, Uno BE, Bromann GL, Clark MJ, Anderson TM, Burke MD.

Nat Chem. 2012 Dec;4(12):996-1003.

10.

(Z)-(2-bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis.

Woerly EM, Struble JR, Palyam N, O'Hara SP, Burke MD.

Tetrahedron. 2011 Jun 17;67(24):4333-4343. No abstract available.

11.

Moderating factors of video-modeling with other as model: a meta-analysis of single-case studies.

Mason RA, Ganz JB, Parker RI, Burke MD, Camargo SP.

Res Dev Disabil. 2012 Jul-Aug;33(4):1076-86. doi: 10.1016/j.ridd.2012.01.016. Epub 2012 Feb 23.

PMID:
22502832
12.

Amphotericin primarily kills yeast by simply binding ergosterol.

Gray KC, Palacios DS, Dailey I, Endo MM, Uno BE, Wilcock BC, Burke MD.

Proc Natl Acad Sci U S A. 2012 Feb 14;109(7):2234-9. doi: 10.1073/pnas.1117280109. Epub 2012 Jan 17.

13.

A general solution for the 2-pyridyl problem.

Dick GR, Woerly EM, Burke MD.

Angew Chem Int Ed Engl. 2012 Mar 12;51(11):2667-72. doi: 10.1002/anie.201108608. Epub 2012 Jan 27.

14.
15.

Total synthesis of synechoxanthin through iterative cross-coupling.

Fujii S, Chang SY, Burke MD.

Angew Chem Int Ed Engl. 2011 Aug 16;50(34):7862-4. doi: 10.1002/anie.201102688. Epub 2011 Jun 16. No abstract available.

16.

Synthesis-enabled functional group deletions reveal key underpinnings of amphotericin B ion channel and antifungal activities.

Palacios DS, Dailey I, Siebert DM, Wilcock BC, Burke MD.

Proc Natl Acad Sci U S A. 2011 Apr 26;108(17):6733-8. doi: 10.1073/pnas.1015023108. Epub 2011 Feb 28.

17.

A simple and general platform for generating stereochemically complex polyene frameworks by iterative cross-coupling.

Lee SJ, Anderson TM, Burke MD.

Angew Chem Int Ed Engl. 2010 Nov 15;49(47):8860-3. doi: 10.1002/anie.201004911. No abstract available.

18.

General method for synthesis of 2-heterocyclic N-methyliminodiacetic acid boronates.

Dick GR, Knapp DM, Gillis EP, Burke MD.

Org Lett. 2010 May 21;12(10):2314-7. doi: 10.1021/ol100671v.

PMID:
20465293
19.

Stereoretentive Suzuki-Miyaura coupling of haloallenes enables fully stereocontrolled access to (-)-peridinin.

Woerly EM, Cherney AH, Davis EK, Burke MD.

J Am Chem Soc. 2010 May 26;132(20):6941-3. doi: 10.1021/ja102721p.

20.

A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates.

Knapp DM, Gillis EP, Burke MD.

J Am Chem Soc. 2009 May 27;131(20):6961-3. doi: 10.1021/ja901416p.

PMID:
19405470
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