| Year |
Citation |
Score |
| 2008 |
Datta R, Vilekar SA, Fishtik I, Dittami JP. Toward cell circuitry: Topological analysis of enzyme reaction networks via reaction route graphs Physica a: Statistical Mechanics and Its Applications. 387: 3348-3372. DOI: 10.1016/J.Physa.2008.01.070 |
0.318 |
|
| 2003 |
Dittami JP. Explorations of the Heteroatom Directed Photoarylation Reaction. A Review of the Photoinitiated Intramolecular Cycloaddition Reactions of Ylide Systems Cheminform. 34. DOI: 10.1002/CHIN.200345250 |
0.358 |
|
| 1996 |
Dittami JP, Luo Y, Moss D, McGimpsey WG. Photochemistry of Aryl Vinyl Sulfides and Aryl Vinyl Ethers: Evidence for the Formation of Thiocarbonyl and Carbonyl Ylides. The Journal of Organic Chemistry. 61: 6256-6260. PMID 11667464 DOI: 10.1021/Jo9604649 |
0.364 |
|
| 1995 |
Dittami JP, Feng Xu, Hua Qi, Martin MW, Bordner J, Decosta DL, Kiplinger J, Reiche P, Ware R. Photocyclization of α,β-unsaturated amide aldehydes synthesis of jatropham Tetrahedron Letters. 36: 4201-4204. DOI: 10.1016/0040-4039(95)00780-G |
0.377 |
|
| 1995 |
Dittami JP, Feng Xu, Hua Qi, Martin MW, Bordner J, Decosta DL, Kiplinger J, Reiche P, Ware R. Preparation of N-alkyl pyrrolidinones via photocyclization of γ-keto-α,β-unsaturated amides Tetrahedron Letters. 36: 4197-4200. DOI: 10.1016/0040-4039(95)00779-C |
0.312 |
|
| 1992 |
Dittami JP, Nie XY, Nie H, Ramanathan H, Buntel C, Rigatti S, Bordner J, Decosta DL, Williard P. Tandem photocyclization-intramolecular addition reactions of aryl vinyl sulfides. Observation of a novel [2 + 2] cycloaddition-allylic sulfide rearrangement Journal of Organic Chemistry. 57: 1151-1158. DOI: 10.1021/Jo00030A022 |
0.487 |
|
| 1991 |
Dittami JP, Nie XY, Nie H, Ramanathan H, Breining S, Bordner J, Decosta DL, Kiplinger J, Reiche P, Ware R. Intramolecular addition reactions of carbonyl ylides formed during photocyclization of aryl vinyl ethers Journal of Organic Chemistry. 56: 5572-5578. DOI: 10.1021/Jo00019A020 |
0.446 |
|
| 1990 |
Dittami JP, Xiao-Yi N, Buntel CJ, Rigatti S. Photoinitiated intramolecular ylide-alkene cycloaddition reactions Tetrahedron Letters. 31: 3821-3824. DOI: 10.1016/S0040-4039(00)97478-1 |
0.475 |
|
| 1989 |
Dittami JP, Ramanathan H, Breining S. Intramolecular addition reactions during heteroatom directed photoarylation Tetrahedron Letters. 30: 795-798. DOI: 10.1016/S0040-4039(01)80616-X |
0.447 |
|
| 1988 |
Dittami JP, Ramanathan H. Intramolecular radical cyclization reactions. An approach to the indole alkaloids Tetrahedron Letters. 29: 45-48. DOI: 10.1016/0040-4039(88)80012-1 |
0.454 |
|
| 1984 |
Schultz AG, Dittami JP, Lavieri FP, Salowey C, Sundararaman P, Szymula MB. The synthesis and selected chemistry of 6-alkyl-6-carbalkoxy- and 6-alkyl-6-(aminocarbonyl)-2,4-cyclohexadien-1-ones and cyclohexadienone ketals Journal of Organic Chemistry. 49: 4429-4440. DOI: 10.1021/Jo00197A020 |
0.393 |
|
| 1984 |
Schultz AG, Dittami JP. The bicyclo[3.3.1]nonane solution to the problem of vicinal stereochemical control at a substituted cyclohexane ring. A total synthesis of dl-erythro-juvabione Journal of Organic Chemistry. 49: 2615-2618. DOI: 10.1021/Jo00188A020 |
0.336 |
|
| 1984 |
Schultz AG, Dittami JP, Lavieri FP, Salowey C, Sundararaman P, Szymula MB. The synthesis and selected chemistry of 6-alkyl-6-carbalkoxy- and 6-alkyl-6-(aminocarbonyl)-2,4-cyclohexadien-1-ones and cyclohexadienone ketals Journal of Organic Chemistry. 49: 4429-4440. |
0.364 |
|
| 1983 |
Schultz AG, Dittami JP. Intramolecular alkylation route to the bicyclo[3.3.1]nonane ring system. A total synthesis of dl-clovene Journal of Organic Chemistry. 14: 2318-2321. DOI: 10.1021/Jo00162A004 |
0.413 |
|
| 1983 |
Schultz AG, Dittami JP, Myong SO, Sha CK. A new 2-azatricyclo[4.4.0.02,8]decenone synthesis and ketene formation by retro-Diels-Alder reaction Journal of the American Chemical Society. 105: 3273-3279. DOI: 10.1021/Ja00348A051 |
0.467 |
|
| 1983 |
Schultz AG, Dittami JP. Intramolecular alkylation route to the bicyclo[3.3.1]nonane ring system. A total synthesis of dl-clovene Journal of Organic Chemistry. 48: 2318-2321. |
0.363 |
|
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