Year |
Citation |
Score |
2010 |
WILLIAMS DR, OSTERHOUT MH, REDDY JP. ChemInform Abstract: Diastereoselective Hydride Reductions of α-Hydroxy Oximino Ethers. Synthesis of syn-1,2-Amino Alcohols. Cheminform. 24: no-no. DOI: 10.1002/chin.199340127 |
0.588 |
|
2004 |
Williams DR, Osterhout MH, Amato GS. Iodine-induced cyclizations of N-alkoxyaminoalkenes. A stereocontrolled approach to trans-2,6-disubstituted piperidine alkaloids Heterocycles. 64: 45-50. DOI: 10.3987/Com-04-S(P)26 |
0.545 |
|
1997 |
Padwa A, Brodney MA, Marino JP, Osterhout MH, Price AT. Tandem Dipolar Cycloaddition-Mannich Cyclization as an Approach to Tricyclic Nitrogen Heterocycles. The Journal of Organic Chemistry. 62: 67-77. PMID 11671365 DOI: 10.1021/Jo9607267 |
0.336 |
|
1994 |
Marino JP, Osterhout MH, Price AT, Sheehan SM, Padwa A. Ethyl 2-diazomalonyl chloride. An efficient diazoacylating reagent Tetrahedron Letters. 35: 849-852. DOI: 10.1016/S0040-4039(00)75980-6 |
0.399 |
|
1994 |
Padwa A, Dean DC, Osterhout MH, Precedo L, Semones MA. Synthesis of functionalized azomethine ylides via the Rh(II)-catalyzed cyclization of α-diazo carbonyls onto imino π-bonds Journal of Organic Chemistry. 59: 5347-5357. |
0.303 |
|
1993 |
Williams DR, Osterhout MH, Reddy JP. Diastereoselective hydride reductions of α-hydroxy oximino ethers. Synthesis of syn-1,2-amino alcohols. Tetrahedron Letters. 34: 3271-3274. DOI: 10.1016/S0040-4039(00)73679-3 |
0.582 |
|
1992 |
Williams DR, Robinson LA, Amato GS, Osterhout MH. A preparation of unsymmetrical .alpha.-diketones The Journal of Organic Chemistry. 57: 3740-3744. DOI: 10.1021/Jo00039A047 |
0.493 |
|
1992 |
Williams DR, Osterhout MH. Stereocontrolled hydride reductions of .beta.-hydroxy oximino ethers Journal of the American Chemical Society. 114: 8750-8751. DOI: 10.1021/Ja00048A086 |
0.334 |
|
1992 |
Williams DR, Robinson LA, Amato GS, Osterhout MH. A preparation of unsymmetrical α-diketones Journal of Organic Chemistry. 57: 3740-3744. |
0.525 |
|
1989 |
Williams DR, Osterhout MH, McGill JM. Anchimeric assistance with intermediary N-alkoxyaziridinium salts. Formation of vicinal aminoalcohols and derivatives Tetrahedron Letters. 30: 1331-1334. DOI: 10.1016/S0040-4039(00)99457-7 |
0.592 |
|
1989 |
Williams DR, Osterhout MH, McGill JM. Intramolecular Cyclizations from N-alkoxyamines. Formation of Dialkylsubstituted pyrrolidines and piperidines Tetrahedron Letters. 30: 1327-1330. DOI: 10.1016/S0040-4039(00)99456-5 |
0.581 |
|
1989 |
WILLIAMS DR, OSTERHOUT MH, MCGILL JM. ChemInform Abstract: Anchimeric Assistance with Intermediary N-Alkoxyaziridinium Salts. Formation of Vicinal Amino Alcohols and Derivatives. Cheminform. 20. DOI: 10.1002/chin.198938209 |
0.465 |
|
1986 |
FRASER-REID B, UNDERWOOD R, OSTERHOUT M, GROSSMAN JA, LIOTTA D. ChemInform Abstract: Some Observations on the Relative Reactivities of α-Enones of Oxanes and Cyclohexanes. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198650093 |
0.315 |
|
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