Year |
Citation |
Score |
2011 |
Benson SC, Lee L, Wei W, Ni F, Olmos JDJ, Strom KR, Beeler AB, Cheng KCC, Inglese J, Kota S, Takahashi V, Strosberg AD, Connor JH, Bushkin GG, Snyder JK. Truncated aspidosperma alkaloid-like scaffolds: Unique structures for the discovery of new, bioactive compounds Heterocycles. 84: 135-155. DOI: 10.3987/Rev-11-Sr(P)4 |
0.602 |
|
2000 |
Benson SC, Lee L, Yang L, Snyder JK. Intramolecular inverse electron demand Diels-Alder reactions of tryptamine with tethered heteroaromatic azadienes Tetrahedron. 56: 1165-1180. DOI: 10.1016/S0040-4020(00)00003-X |
0.667 |
|
1996 |
Benson SC, Lee L, Snyder JK. Inverse electron demand Diels-Alder reactions of indole V. Reactions of 3-substituted indoles with heteroaromatic azadienes Tetrahedron Letters. 37: 5061-5064. DOI: 10.1016/0040-4039(96)01017-9 |
0.681 |
|
1992 |
Benson SC, Li JH, Snyder JK. Indole as a dienophile in inverse electron demand diels-alder reactions. 3. Intramolecular reactions with 1,2,4-triazines to access the canthine skeleton Journal of Organic Chemistry. 57: 5285-5287. DOI: 10.1021/Jo00046A005 |
0.605 |
|
1991 |
Benson SC, Snyder JK. Optically pure chiral sulfoxides using ephedrine as a chiral auxiliary Tetrahedron Letters. 32: 5885-5888. DOI: 10.1016/S0040-4039(00)79417-2 |
0.652 |
|
1990 |
Benson SC, Gross JL, Snyder JK. Indole as a dienophile in inverse electron demand Diels-Alder reactions: Reactions with 1,2,4-triazines and 1,2-diazines Journal of Organic Chemistry. 55: 3257-3269. DOI: 10.1021/Jo00297A050 |
0.612 |
|
1988 |
Benson SC, Cai P, Colon M, Haiza MA, Tokles M, Snyder JK. Use of carboxylic acids as chiral solvating agents for the determination of optical purity of chiral amines by NMR spectroscopy Journal of Organic Chemistry. 53: 5335-5341. DOI: 10.1021/Jo00257A024 |
0.446 |
|
1987 |
Benson SC, Palabrica CA, Snyder JK. Indole as a dienophile in inverse electron demand Diels-Alder reactions. 5H-pyridazino[4,5-6]indoles as cycloadducts with 3,6-dicarbomethoxy-1,2,4,5-tetrazine Journal of Organic Chemistry. 52: 4610-4614. DOI: 10.1021/Jo00229A034 |
0.599 |
|
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