| Year |
Citation |
Score |
| 2003 |
Almond MR, Stimmel JB, Thompson EA, Loudon GM. Hofmann Rearrangement Under Mildly Acidic Conditions Using [I,I‐Bis(Trifluoroacetoxy)]Iodobenzene: Cyclobutylamine Hydrochloride from Cyclobutanecarboxamide Organic Syntheses. 132-132. DOI: 10.1002/0471264180.Os066.18 |
0.34 |
|
| 1995 |
Boyd VL, Bozzini M, Guga PJ, DeFranco RJ, Yuan PM, Loudon GM, Nguyen D. Activation of the carboxy terminus of a peptide for carboxy-terminal sequencing Journal of Organic Chemistry. 60: 2581-2587. DOI: 10.1021/Jo00113A042 |
0.314 |
|
| 1992 |
Geahlen RL, Loudon GM, Paige LA, Lloyd D. A general method for preparation of peptides biotinylated at the carboxy terminus. Analytical Biochemistry. 202: 68-70. PMID 1621986 DOI: 10.1016/0003-2697(92)90207-N |
0.387 |
|
| 1989 |
Blodgett JK, Loudon GM. Direct cleavage versus transpeptidation in the autodecomposition of peptides containing 2,4-diaminobutanoic acid (DABA) and 2,3-diaminopropanoic acid (DAPA) residues. Specific cleavage of DAPA-containing peptides Journal of the American Chemical Society. 111: 6813-6821. DOI: 10.1021/Ja00199A049 |
0.412 |
|
| 1985 |
Blodgett JK, Loudon GM, Collins KD. Specific cleavage of peptides containing an aspartic acid (β-hydroxamic acid) residue Journal of the American Chemical Society. 107: 4305-4313. |
0.308 |
|
| 1983 |
Capecchi JT, Miller MJ, Loudon GM. Critical examination of a method for the analysis of .alpha. and .omega. linkages in peptides containing aspartic acid and glutamic acid The Journal of Organic Chemistry. 48: 2014-2021. DOI: 10.1021/Jo00160A015 |
0.49 |
|
| 1983 |
Capecchi JT, Miller MJ, Loudon GM. Critical examination of a method for the analysis of α and ω linkages in peptides containing aspartic acid and glutamic acid Journal of Organic Chemistry. 48: 2014-2021. |
0.306 |
|
| 1980 |
DeBons FE, Loudon GM. Tryptic cleavage of a peptide at modified aspartic acid. Biochemical and Biophysical Research Communications. 92: 606-9. PMID 7356484 DOI: 10.1016/0006-291X(80)90376-9 |
0.322 |
|
| 1979 |
Lee CC, Loudon GM. Quantitative determination of amino groups on derivatized controlled pore glass: a comparison of methods. Analytical Biochemistry. 94: 60-4. PMID 464285 DOI: 10.1016/0003-2697(79)90790-5 |
0.326 |
|
| 1978 |
Loudon GM, Parham ME. New reagents for carboxyl-terminal peptide sequencing Tetrahedron Letters. 19: 437-440. DOI: 10.1016/S0040-4039(01)91448-0 |
0.342 |
|
| 1977 |
Miller MJ, DeBons FE, Loudon GM. The chemistry of a method for the determination of carboxyl-terminal residues in peptides. The Journal of Organic Chemistry. 42: 1750-61. PMID 853324 DOI: 10.1002/Chin.197742366 |
0.435 |
|
| 1975 |
Miller MJ, Loudon GM. Letter: Carboxyl-terminal amino acid residue analysis of peptides. A new method. Journal of the American Chemical Society. 97: 5295-7. PMID 1165365 DOI: 10.1021/Ja00851A055 |
0.482 |
|
| 1970 |
Loudon GM, Koshland DE. The chemistry of a reporter group: 2-hydroxy-5-nitrobenzyl bromide. The Journal of Biological Chemistry. 245: 2247-54. PMID 5442270 |
0.326 |
|
| 1970 |
Noyce DS, Lipinski CA, Loudon GM. Correlation of the reactivity of thiophene derivatives Journal of Organic Chemistry. 35: 1718-1720. |
0.435 |
|
| 1969 |
Loudon GM, Portsmouth D, Lukton A, Koshland DE. The chemistry of the modification of tryptophan with 2-hydroxy-5-nitrobenzyl bromide. Journal of the American Chemical Society. 91: 2792-4. PMID 5784953 DOI: 10.1021/Ja01038A068 |
0.403 |
|
| 1969 |
Loudon GM, Noyce DS. General acid catalysis in the dehydration of 1-aryl-2-phenylethanols Journal of the American Chemical Society. 91: 1433-1437. DOI: 10.1021/Ja01034A028 |
0.497 |
|
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