Year |
Citation |
Score |
2018 |
Hostetler MA, Lipton MA. An Optimized Preparation of 1,1-Dimethylallyl Esters and Their Application to Solid-Phase Peptide Synthesis. The Journal of Organic Chemistry. PMID 29938510 DOI: 10.1021/Acs.Joc.8B00658 |
0.801 |
|
2016 |
Rindelaub JD, Borca CH, Hostetler MA, Slade JH, Lipton MA, Slipchenko LV, Shepson PB. The acid-catalyzed hydrolysis of an α-pinene-derived organic nitrate: kinetics, products, reaction mechanisms, and atmospheric impact Atmospheric Chemistry and Physics. 16: 15425-15432. DOI: 10.5194/Acp-16-15425-2016 |
0.756 |
|
2015 |
Xiong F, McAvey KM, Pratt KA, Groff CJ, Hostetler MA, Lipton MA, Starn TK, Seeley JV, Bertman SB, Teng AP, Crounse JD, Nguyen TB, Wennberg PO, Misztal PK, Goldstein AH, et al. Observation of isoprene hydroxynitrates in the southeastern United States and implications for the fate of NOx Atmospheric Chemistry and Physics. 15: 11257-11272. DOI: 10.5194/Acp-15-11257-2015 |
0.749 |
|
2013 |
St John SE, Jensen KC, Kang S, Chen Y, Calamini B, Mesecar AD, Lipton MA. Design, synthesis, biological and structural evaluation of functionalized resveratrol analogues as inhibitors of quinone reductase 2. Bioorganic & Medicinal Chemistry. 21: 6022-37. PMID 23953689 DOI: 10.1016/J.Bmc.2013.07.037 |
0.724 |
|
2013 |
Yang L, Bekele T, Lipton MA, Kenttämaa HI. Generation and characterization of a distonic biradical anion formed from an enediynone prodrug in the gas phase. Journal of the American Society For Mass Spectrometry. 24: 563-72. PMID 23512422 DOI: 10.1007/S13361-012-0567-8 |
0.616 |
|
2009 |
Kang SS, Cuendet M, Endringer DC, Croy VL, Pezzuto JM, Lipton MA. Synthesis and biological evaluation of a library of resveratrol analogues as inhibitors of COX-1, COX-2 and NF-kappaB. Bioorganic & Medicinal Chemistry. 17: 1044-54. PMID 18487053 DOI: 10.1016/J.Bmc.2008.04.031 |
0.569 |
|
2008 |
Ramamoorthy G, Acevedo CM, Alvira E, Lipton MA. Synthesis and Spectroscopic Correlation of the Diastereoisomers of 2,3-Dihydroxy-2,6,8-trimethyldeca-(4Z, 6E)-dienoic Acid: Implications for the Structures of Papuamides A-D and Mirabamides A-D. Tetrahedron, Asymmetry. 19: 2546-2554. PMID 24163502 DOI: 10.1016/J.Tetasy.2008.09.031 |
0.793 |
|
2007 |
Cranfill DC, Lipton MA. Enantio- and diastereoselective synthesis of (R,R)-beta-methoxytyrosine. Organic Letters. 9: 3511-3. PMID 17676746 DOI: 10.1021/Ol071350U |
0.778 |
|
2007 |
Krishnamoorthy R, Richardson BL, Lipton MA. Synthesis and cytotoxicity of desmethoxycallipeltin B: lack of a quinone methide for the cytotoxicity of callipeltin B. Bioorganic & Medicinal Chemistry Letters. 17: 5136-8. PMID 17643303 DOI: 10.1016/J.Bmcl.2007.07.003 |
0.553 |
|
2006 |
Sedighi M, Calimsiz S, Lipton MA. An improved method for the protection of carboxylic acids as 1,1-dimethylallyl esters. The Journal of Organic Chemistry. 71: 9517-8. PMID 17137386 DOI: 10.1021/Jo061207Z |
0.795 |
|
2006 |
Krishnamoorthy R, Vazquez-Serrano LD, Turk JA, Kowalski JA, Benson AG, Breaux NT, Lipton MA. Solid-phase total synthesis and structure proof of callipeltin B. Journal of the American Chemical Society. 128: 15392-3. PMID 17132003 DOI: 10.1021/Ja0666250 |
0.637 |
|
2006 |
Waddell MK, Bekele T, Lipton MA. Ring size and substituent effects in oxyanion-promoted cyclizations of enyne-allenes: observation of a Myers-Saito cycloaromatization at cryogenic temperature. The Journal of Organic Chemistry. 71: 8372-7. PMID 17064007 DOI: 10.1021/Jo061088N |
0.718 |
|
2006 |
Calimsiz S, Morales Ramos AI, Lipton MA. Solid-phase synthesis and configurational reassigment of callipeltin E. Implications for the structures of callipeltins A and B. The Journal of Organic Chemistry. 71: 6351-6. PMID 16901115 DOI: 10.1021/Jo060351H |
0.791 |
|
2006 |
Cranfill DC, Morales-Ramos ÁI, Lipton MA. Solid-Phase Synthesis of Callipeltin D Synfacts. 2006: 285-285. DOI: 10.1055/S-2006-931999 |
0.751 |
|
2005 |
Cranfill DC, Morales-Ramos AI, Lipton MA. Solid-phase synthesis of callipeltin D. Stereochemical confirmation of the unnatural amino acid AGDHE. Organic Letters. 7: 5881-3. PMID 16354090 DOI: 10.1021/Ol052438F |
0.795 |
|
2005 |
Oku N, Krishnamoorthy R, Benson AG, Ferguson RL, Lipton MA, Phillips LR, Gustafson KR, McMahon JB. Complete stereochemistry of neamphamide A and absolute configuration of the beta-methoxytyrosine residue in papuamide B. The Journal of Organic Chemistry. 70: 6842-7. PMID 16095304 DOI: 10.1021/Jo0508853 |
0.634 |
|
2005 |
Calimsiz S, Lipton MA. Synthesis of N-Fmoc-(2S,3S,4R)-3,4-dimethylglutamine: An application of lanthanide-catalyzed transamidation. The Journal of Organic Chemistry. 70: 6218-21. PMID 16050680 DOI: 10.1021/Jo050518R |
0.799 |
|
2005 |
Bekele T, Christian CF, Lipton MA, Singleton DA. "Concerted" transition state, stepwise mechanism. Dynamics effects in C2-C6 enyne allene cyclizations. Journal of the American Chemical Society. 127: 9216-23. PMID 15969600 DOI: 10.1021/Ja0508673 |
0.614 |
|
2005 |
Sedighi M, Lipton MA. A convenient, general synthesis of 1,1-dimethylallyl esters as protecting groups for carboxylic acids. Organic Letters. 7: 1473-5. PMID 15816730 DOI: 10.1021/Ol0476117 |
0.66 |
|
2005 |
Barth BS, Myers AC, Lipton MA. Exploring the stereochemical requirements for protease inhibition by ureidopeptides. The Journal of Peptide Research : Official Journal of the American Peptide Society. 65: 352-4. PMID 15787965 DOI: 10.1111/j.1399-3011.2005.00224.x |
0.76 |
|
2004 |
Myers AC, Kowalski JA, Lipton MA. Facile incorporation of urea pseudopeptides into protease substrate analogue inhibitors. Bioorganic & Medicinal Chemistry Letters. 14: 5219-22. PMID 15380231 DOI: 10.1016/J.Bmcl.2004.07.092 |
0.561 |
|
2004 |
Hess S, Gustafson KR, Milanowski DJ, Alvira E, Lipton MA, Pannell LK. Chirality determination of unusual amino acids using precolumn derivatization and liquid chromatography-electrospray ionization mass spectrometry. Journal of Chromatography. A. 1035: 211-9. PMID 15124814 DOI: 10.1016/J.Chroma.2004.02.068 |
0.375 |
|
2003 |
Bekele T, Brunette SR, Lipton MA. Synthesis and cycloaromatization of a cyclic enyne-allene prodrug. The Journal of Organic Chemistry. 68: 8471-9. PMID 14575473 DOI: 10.1021/Jo034278W |
0.665 |
|
2003 |
Turk JA, Visbal GS, Lipton MA. Asymmetric synthesis of four diastereomers of 3-hydroxy-2,4,6-trimethylheptanoic acid: proof of configurational assignment. The Journal of Organic Chemistry. 68: 7841-4. PMID 14510564 DOI: 10.1021/Jo034738L |
0.409 |
|
2003 |
Thoen JC, Morales-Ramos AI, Lipton MA. Synthesis of the Unnatural Amino Acid AGDHE (I), a Constituent of the Cyclic Depsipeptides Callipeltins A (II) and D (III). Cheminform. 34. DOI: 10.1002/chin.200317168 |
0.788 |
|
2002 |
Thoen JC, Morales-Ramos AI, Lipton MA. Synthesis of the unnatural amino acid AGDHE, a constituent of the cyclic depsipeptides callipeltins A and D. Organic Letters. 4: 4455-8. PMID 12465911 DOI: 10.1021/Ol0269852 |
0.818 |
|
2001 |
Acevedo CM, Kogut EF, Lipton MA. Synthesis and analysis of the sterically constrained L-glutamine analogues (3S,4R)-3,4-dimethyl-L-glutamine and (3S,4R)-3,4-dimethyl-L-pyroglutamic acid Tetrahedron. 57: 6353-6359. DOI: 10.1016/S0040-4020(01)00501-4 |
0.785 |
|
2000 |
Brunette SR, Lipton MA. Oxyanion-accelerated C2-C6 cyclization of benzannulated enyne-allenes The Journal of Organic Chemistry. 65: 5114-9. PMID 10993334 DOI: 10.1021/Jo991876V |
0.341 |
|
2000 |
Wenthold PG, Lipton MA. A density functional molecular orbital study of the C2-C7 and C2-C6 cyclization pathways of 1,2,4-heptatrien-6-ynes. The role of benzannulation Journal of the American Chemical Society. 122: 9265-9270. DOI: 10.1021/Ja002050+ |
0.311 |
|
1999 |
Yong YF, Kowalski JA, Thoen JC, Lipton MA. A new reagent for solid and solution phase synthesis of protected guanidines from amines Tetrahedron Letters. 40: 53-56. DOI: 10.1016/S0040-4039(98)80017-8 |
0.781 |
|
1998 |
Kogut EF, Thoen JC, Lipton MA. Examination and Enhancement of Enantioselective Autoinduction in Cyanohydrin Formation by Cyclo[ (R)-His- (R)-Phe] Journal of Organic Chemistry. 63: 4604-4610. DOI: 10.1021/Jo972238K |
0.793 |
|
1997 |
Yong YF, Kowalski JA, Lipton MA. Facile and Efficient Guanylation of Amines Using Thioureas and Mukaiyama's Reagent The Journal of Organic Chemistry. 62: 1540-1542. DOI: 10.1021/Jo962196K |
0.311 |
|
1997 |
Thoen JC, Lipton MA. The effects of N-methylation on the enantioselectivity of catalysis by cyclo[(R)-His-(R)-Phe] Tetrahedron Asymmetry. 8: 3947-3954. DOI: 10.1016/S0957-4166(97)00573-9 |
0.79 |
|
1996 |
Iyer MS, Gigstad KM, Namdev ND, Lipton M. Asymmetric catalysis of the Strecker amino acid synthesis by a cyclic dipeptide Amino Acids. 11: 259-268. DOI: 10.1021/Ja952686E |
0.435 |
|
1996 |
Kowalski J, Lipton MA. Solid phase synthesis of a diketopiperazine catalyst containing the unnatural amino acid (S)-norarginine Tetrahedron Letters. 37: 5839-5840. DOI: 10.1016/0040-4039(96)01239-7 |
0.466 |
|
1994 |
Etzkorn FA, Guo T, Lipton MA, Goldberg SD, Bartlett PA. Cyclic hexapeptides and chimeric peptides as mimics of tendamistat Journal of the American Chemical Society. 116: 10412-10425. DOI: 10.1021/Ja00102A008 |
0.686 |
|
1993 |
Iyer MS, Lipton MA. An improved synthesis of the diketopiperazine catalyst cyclo[(S)-HIS-(S)-PHE] Bioorganic and Medicinal Chemistry Letters. 3: 2061-2062. DOI: 10.1016/S0960-894X(01)81015-5 |
0.335 |
|
1993 |
Yong YF, Lipton MA. The stereoselective synthesis of (E)-alkene dipeptide isosteres Bioorganic and Medicinal Chemistry Letters. 3: 2879-2882. DOI: 10.1016/S0960-894X(01)80783-6 |
0.34 |
|
1993 |
Morin-Fox ML, Lipton MA. Stereodivergence in an intramolecular Horner-Emmons macrocyclization. Effect of reaction conditions on product distribution Tetrahedron Letters. 34: 7899-7902. DOI: 10.1016/S0040-4039(00)61505-8 |
0.326 |
|
1990 |
Saunders M, Houk KN, Wu YD, Still WC, Lipton M, Chang G, Guida WC. Conformations of cycloheptadecane. A comparison of methods for conformational searching Journal of the American Chemical Society. 112: 1419-1427. DOI: 10.1021/Ja00160A020 |
0.496 |
|
1990 |
Saunders M, Houk KN, Wu YD, Still WC, Lipton M, Chang G, Guida WC. Conformations of cycloheptadecane. A comparison of methods for conformational searching Journal of the American Chemical Society. 112: 1419-1427. |
0.44 |
|
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