Year |
Citation |
Score |
2020 |
Hu Z, Lin G, Sender M, Cannon KC, Davis FA, Krow GR. C6-Substituted methanopyrrolidine β-amino acid: synthesis and characterization of oligomeric foldamers Tetrahedron Letters. 61: 152240. DOI: 10.1016/J.Tetlet.2020.152240 |
0.621 |
|
2010 |
Krow GR, Liu N, Sender M, Lin G, Centafont R, Sonnet PE, DeBrosse C, Ross CW, Carroll PJ, Shoulders MD, Raines RT. Oligomers of a 5-carboxy-methanopyrrolidine β-amino acid. A search for order. Organic Letters. 12: 5438-41. PMID 21043445 DOI: 10.1021/Ol1022917 |
0.636 |
|
2009 |
Krow GR, Edupuganti R, Gandla D, Choudhary A, Lin G, Sonnet PE, DeBrosse C, Ross CW, Cannon KC, Raines RT. 5(6)-anti-Substituted-2-azabicyclo[2.1.1]hexanes: a nucleophilic displacement route. The Journal of Organic Chemistry. 74: 8232-42. PMID 19799411 DOI: 10.1021/Jo901725K |
0.663 |
|
2008 |
Krow GR, Gandla D, Guo W, Centafont RA, Lin G, Debrosse C, Sonnet PE, Iii CW, Ramjit HG, Cannon KC. Selectfluor as a nucleofuge in the reactions of azabicyclo[n.2.1]alkane beta-halocarbamic acid esters (n = 2,3). The Journal of Organic Chemistry. 73: 2122-9. PMID 18290657 DOI: 10.1021/Jo702155V |
0.646 |
|
2008 |
Krow GR, Gandla D, Guo W, Centafont RA, Lin G, DeBrosse C, Sonnet PE, Iii CW, Ramjit HG, Carroll PJ, Cannon KC. Neighboring group participation in the additions of iodonium and bromonium ions to N-alkoxycarbonyl-2-azabicyclo[2.2.n]alk-5-enes (n = 1,2). The Journal of Organic Chemistry. 73: 2114-21. PMID 18290656 DOI: 10.1021/Jo702153Q |
0.654 |
|
2006 |
Krow GR, Huang Q, Lin G, Centafont RA, Thomas AM, Gandla D, Debrosse C, Carroll PJ. 5-Carboxy-2-azabicyclo[2.1.1]hexanes as precursors of 5-halo, amino, phenyl, and 2-methoxycarbonylethyl methanopyrrolidines. The Journal of Organic Chemistry. 71: 2090-8. PMID 16496997 DOI: 10.1021/Jo052506B |
0.669 |
|
2005 |
Krow GR, Lin G, Yu F. The rearrangement route to 3-carboxy- and 3-hydroxymethyl-2-azabicyclo[2.1.1]hexanes: 3,5-methanoprolines. The Journal of Organic Chemistry. 70: 590-5. PMID 15651806 DOI: 10.1021/Jo0484171 |
0.652 |
|
2004 |
Jenkins CL, Lin G, Duo J, Rapolu D, Guzei IA, Raines RT, Krow GR. Substituted 2-azabicyclo[2.1.1]hexanes as constrained proline analogues: implications for collagen stability. The Journal of Organic Chemistry. 69: 8565-73. PMID 15575731 DOI: 10.1021/Jo049242Y |
0.626 |
|
2004 |
Krow GR, Lin G, Moore KP, Thomas AM, DeBrosse C, Ross CW, Ramjit HG. Novel selectfluor and deoxo-fluor-mediated rearrangements. New 5(6)-methyl and phenyl methanopyrrolidine alcohols and fluorides. Organic Letters. 6: 1669-72. PMID 15128263 DOI: 10.1021/Ol0494818 |
0.604 |
|
2003 |
Krow GR, Lin G, Herzon SB, Thomas AM, Moore KP, Huang Q, Carroll PJ. Convenient preparations of 2,4-methanopyrrolidine and 5-carboxy-2,4-methanopyrrolidines. The Journal of Organic Chemistry. 68: 7562-4. PMID 12968923 DOI: 10.1021/Jo0348672 |
0.687 |
|
2003 |
Krow GR, Lin G, Yu F, Sonnet PE. Second-chance rearrangement route to novel 5(6)-syn,anti-difunctional 2-azabicyclo[2.1.1]hexanes. Organic Letters. 5: 2739-41. PMID 12868903 DOI: 10.1021/Ol0349662 |
0.661 |
|
2003 |
Krow GR, Lin G, Rapolu D, Fang Y, Lester WS, Herzon SB, Sonnet PE. The rearrangement route to 2-azabicyclo[2.1.1]hexanes. Solvent and electrophile control of neighboring group participation. The Journal of Organic Chemistry. 68: 5292-9. PMID 12816491 DOI: 10.1021/Jo034394Z |
0.588 |
|
2003 |
Krow GR, Lester WS, Lin G, Fang Y, Carroll PJ. Chlorosulfonyl isocyanate reactions with N-(alkoxycarbonyl)-2-azabicyclo[2.2.0]hex-5-enes. Regiospecific two-atom insertion pathways. The Journal of Organic Chemistry. 68: 1626-9. PMID 12585922 DOI: 10.1021/Jo020655D |
0.735 |
|
2002 |
Krow GR, Herzon SB, Lin G, Qiu F, Sonnet PE. Complex-induced proximity effects. Temperature-dependent regiochemical diversity in lithiation-electrophilic substitution reactions of N-BOC-2-azabicyclo[2.1.1]hexane. 2,4- and 3,5-methanoprolines. Organic Letters. 4: 3151-4. PMID 12201739 DOI: 10.1021/Ol026509B |
0.644 |
|
2002 |
Krow GR, Yuan J, Lin G, Sonnet PE. The rearrangement route to 3-CH(2)X-2-azabicyclo[2.1.1]hexanes. Substituent control of neighboring group participation. Organic Letters. 4: 1259-62. PMID 11950337 DOI: 10.1021/Ol020007G |
0.624 |
|
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