Year |
Citation |
Score |
2023 |
Scesa PD, Roche SP, West L. Enantioselective Synthesis of (+)-Providencin and Its Unexpected Regioisomer via a Biomimetic Norrish-Yang Cyclization from (-)-Bipinnatin E. Organic Letters. PMID 38096813 DOI: 10.1021/acs.orglett.3c03604 |
0.307 |
|
2021 |
Scesa PD, West LM, Roche SP. Role of Macrocyclic Conformational Steering in a Kinetic Route toward Bielschowskysin. Journal of the American Chemical Society. 143: 7566-7577. PMID 33945689 DOI: 10.1021/jacs.1c03336 |
0.308 |
|
2021 |
Roche SP. Recent Advances in Oxa-6π Electrocyclization Reactivity for the Synthesis of Privileged Natural Product Scaffolds Organics. 2: 376-387. DOI: 10.3390/org2040021 |
0.352 |
|
2019 |
Shearer C, Desaunay O, Zorc S, Richaud AD, Samanta SS, Jeedimalla N, Roche SP. Intercepted-Knoevenagel condensation for the synthesis of unsymmetrical fused-tricyclic 4-pyrans. Tetrahedron. 75. PMID 31741543 DOI: 10.1016/j.tet.2019.130606 |
0.315 |
|
2019 |
Zaghouani M, Bögeholz LAK, Mercier E, Wintermeyer W, Roche SP. Total synthesis of (±)-fumimycin and analogues for biological evaluation as peptide deformylase inhibitors. Tetrahedron. 75: 3216-3230. PMID 31555018 DOI: 10.1016/j.tet.2019.03.037 |
0.317 |
|
2017 |
Scesa P, Wangpaichitr M, Savaraj N, West L, Roche SP. A Kinetic Dearomatization Strategy for an Expedient Biomimetic Route to the Bielschowskysin Skeleton. Angewandte Chemie (International Ed. in English). PMID 29232501 DOI: 10.1002/Anie.201711780 |
0.33 |
|
2013 |
Santagata S, Mendillo ML, Tang YC, Subramanian A, Perley CC, Roche SP, Wong B, Narayan R, Kwon H, Koeva M, Amon A, Golub TR, Porco JA, Whitesell L, Lindquist S. Tight coordination of protein translation and HSF1 activation supports the anabolic malignant state. Science (New York, N.Y.). 341: 1238303. PMID 23869022 DOI: 10.1126/Science.1238303 |
0.412 |
|
2013 |
Jeedimalla N, Johns J, Roche SP. Mechanistic investigation and implications of a sacrificial aniline for the tandem cascade synthesis of 4-aza-podophyllotoxin analogues Tetrahedron Letters. 54: 5845-5848. DOI: 10.1016/j.tetlet.2013.08.071 |
0.336 |
|
2012 |
Lajkiewicz NJ, Roche SP, Gerard B, Porco JA. Enantioselective photocycloaddition of 3-hydroxyflavones: total syntheses and absolute configuration assignments of (+)-ponapensin and (+)-elliptifoline. Journal of the American Chemical Society. 134: 13108-13. PMID 22804454 DOI: 10.1021/Ja305342F |
0.552 |
|
2012 |
Rodrigo CM, Cencic R, Roche SP, Pelletier J, Porco JA. Synthesis of rocaglamide hydroxamates and related compounds as eukaryotic translation inhibitors: synthetic and biological studies. Journal of Medicinal Chemistry. 55: 558-62. PMID 22128783 DOI: 10.1021/Jm201263K |
0.563 |
|
2011 |
Roche SP, Porco JA. Dearomatization strategies in the synthesis of complex natural products. Angewandte Chemie (International Ed. in English). 50: 4068-93. PMID 21506209 DOI: 10.1002/anie.201006017 |
0.603 |
|
2011 |
Roche SP, Aitken DJ. ChemInform Abstract: Chemistry of 4-Hydroxy-2-cyclopentenone Derivatives Cheminform. 42: no-no. DOI: 10.1002/CHIN.201106221 |
0.542 |
|
2010 |
Roche SP, Cencic R, Pelletier J, Porco JA. Biomimetic photocycloaddition of 3-hydroxyflavones: synthesis and evaluation of rocaglate derivatives as inhibitors of eukaryotic translation. Angewandte Chemie (International Ed. in English). 49: 6533-8. PMID 20687060 DOI: 10.1002/Anie.201003212 |
0.521 |
|
2010 |
Roche SP, Teyssot ML, Gautier A. Synthesis of 1,2 diamines under environmentally benign conditions: application for the preparation of imidazolidiniums Tetrahedron Letters. 51: 1265-1268. DOI: 10.1016/J.Tetlet.2009.12.072 |
0.472 |
|
2010 |
Roche SP, Aitken DJ. Chemistry of 4-hydroxy-2-cyclopentenone derivatives European Journal of Organic Chemistry. 5339-5358. DOI: 10.1002/ejoc.201000704 |
0.535 |
|
2009 |
Teyssot ML, Jarrousse AS, Manin M, Chevry A, Roche S, Norre F, Beaudoin C, Morel L, Boyer D, Mahiou R, Gautier A. Metal-NHC complexes: a survey of anti-cancer properties. Dalton Transactions (Cambridge, England : 2003). 6894-902. PMID 20449127 DOI: 10.1039/B906308K |
0.396 |
|
2009 |
Faure S, Hjelmgaard T, Roche SP, Aitken DJ. Passerini reaction-amine deprotection-acyl migration peptide assembly: efficient formal synthesis of cyclotheonamide C. Organic Letters. 11: 1167-70. PMID 19203293 DOI: 10.1021/ol900048r |
0.526 |
|
2008 |
Roche SP, Faure S, Aitken DJ. Total synthesis of cyclotheonamide C using a tandem backbone-extension-coupling methodology. Angewandte Chemie (International Ed. in English). 47: 6840-2. PMID 18661464 DOI: 10.1002/anie.200802005 |
0.544 |
|
2008 |
Roche SP, Faure S, El Blidi L, Aitken DJ. Total synthesis of cyclotheonamide C by use of an α-keto cyanophosphorane methodology for peptide assembly European Journal of Organic Chemistry. 5067-5078. DOI: 10.1002/ejoc.200800591 |
0.519 |
|
2004 |
Aitken DJ, Faure S, Roche S. Synthetic Approaches to the Southern Part (I) of Cyclotheonamide C (II). Cheminform. 35. DOI: 10.1002/CHIN.200411173 |
0.472 |
|
2003 |
Aitken DJ, Faure S, Roche S. Synthetic approaches to the southern part of cyclotheonamide C Tetrahedron Letters. 44: 8827-8830. DOI: 10.1016/J.TETLET.2003.09.196 |
0.488 |
|
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