Year |
Citation |
Score |
2019 |
Craig RA, Smith RC, Roizen JL, Jones AC, Virgil SC, Stoltz BM. Unified Enantioselective, Convergent Synthetic Approach Toward the Furanobutenolide-Derived Polycyclic Norcembranoid Diterpenes: Synthesis of a Series of Ineleganoloids by Oxidation State Manipulation of the Carbocyclic Core. The Journal of Organic Chemistry. PMID 31066273 DOI: 10.1021/Acs.Joc.9B00635 |
0.748 |
|
2019 |
Craig RA, Roizen JL, Smith RC, Jones AC, Virgil SC, Stoltz BM. Correction: Enantioselective, convergent synthesis of the ineleganolide core by a tandem annulation cascade. Chemical Science. 10: 1254-1255. PMID 30774926 DOI: 10.1039/C8Sc90236D |
0.739 |
|
2018 |
Craig RA, Smith RC, Roizen JL, Jones AC, Virgil SC, Stoltz BM. The Development of a Unified Enantioselective, Convergent Synthetic Approach Toward the Furanobutenolide-Derived Polycyclic Norcembranoid Diterpenes: Asymmetric Formation of the Polycyclic Norditerpenoid Carbocyclic Core by Tandem Annulation Cascade. The Journal of Organic Chemistry. PMID 29464957 DOI: 10.1021/Acs.Joc.7B02825 |
0.782 |
|
2017 |
Craig RA, Stoltz BM. Polycyclic Furanobutenolide-Derived Cembranoid and Norcembranoid Natural Products: Biosynthetic Connections and Synthetic Efforts. Chemical Reviews. PMID 28520418 DOI: 10.1021/Acs.Chemrev.7B00083 |
0.564 |
|
2017 |
Craig RA, Roizen JL, Smith RC, Jones AC, Virgil SC, Stoltz BM. Enantioselective, Convergent Synthesis of the Ineleganolide Core by a Tandem Annulation Cascade. Chemical Science. 8: 507-514. PMID 28239443 DOI: 10.1039/C6Sc03347D |
0.787 |
|
2016 |
Craig RA, Smith RC, Pritchett BP, Estipona BI, Stoltz BM. Preparation of 1,5-Dioxaspiro[5.5]undecan-3-one. Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 93: 210-227. PMID 28729749 DOI: 10.15227/Orgsyn.093.0210 |
0.593 |
|
2016 |
Estipona BI, Pritchett BP, Craig RA, Stoltz BM. Catalytic enantioselective total synthesis of (+)-eucomic acid. Tetrahedron. 72: 3707-3712. PMID 27546916 DOI: 10.1016/J.Tet.2016.02.059 |
0.651 |
|
2015 |
Marziale AN, Duquette DC, Craig RA, Kim KE, Liniger M, Numajiri Y, Stoltz BM. An Efficient Protocol for the Palladium-catalyzed Asymmetric Decarboxylative Allylic Alkylation Using Low Palladium Concentrations and a Palladium(II) Precatalyst. Advanced Synthesis & Catalysis. 357: 2238-2245. PMID 27042171 DOI: 10.1002/Adsc.201500253 |
0.654 |
|
2015 |
Craig RA, Loskot SA, Mohr JT, Behenna DC, Harned AM, Stoltz BM. Palladium-Catalyzed Enantioselective Decarboxylative Allylic Alkylation of Cyclopentanones. Organic Letters. 17: 5160-3. PMID 26501770 DOI: 10.1021/Acs.Orglett.5B02376 |
0.72 |
|
2015 |
Craig RA, Stoltz BM. Synthesis and Exploration of Electronically Modified (R)-5,5-Dimethyl-(p-CF3)3-i-PrPHOX in Palladium-Catalyzed Enantio- and Diastereoselective Allylic Alkylation: A Practical Alternative to (R)-(p-CF3)3-t-BuPHOX. Tetrahedron Letters. 56: 4670-4673. PMID 26257445 DOI: 10.1016/J.Tetlet.2015.06.039 |
0.544 |
|
2015 |
Goldberg AF, Craig RA, O'Connor NR, Stoltz BM. Highly functionalized donor-acceptor cyclopropanes applied toward the synthesis of the Melodinus alkaloids. Tetrahedron Letters. 56: 2983-2990. PMID 26120207 DOI: 10.1016/J.Tetlet.2014.09.016 |
0.736 |
|
2015 |
Craig RA, Stoltz BM. Synthesis and exploration of electronically modified (R)-5,5-dimethyl-(p-CF3)3-i-PrPHOX in palladium-catalyzed enantio- and diastereoselective allylic alkylation: A practical alternative to (R)-(p-CF3)3-t-BuPHOX Tetrahedron Letters. DOI: 10.1016/j.tetlet.2015.06.039 |
0.478 |
|
2015 |
Goldberg AFG, Craig RA, O'Connor NR, Stoltz BM. Highly functionalized donor-acceptor cyclopropanes applied toward the synthesis of the Melodinus alkaloids Tetrahedron Letters. 56: 2983-2990. DOI: 10.1016/j.tetlet.2014.09.016 |
0.651 |
|
2015 |
Marziale AN, Duquette DC, Craig RA, Kim KE, Liniger M, Numajiri Y, Stoltz BM. An Efficient Protocol for the Palladium-Catalyzed Asymmetric Decarboxylative Allylic Alkylation Using Low Palladium Concentrations and a Palladium(II) Precatalyst Advanced Synthesis and Catalysis. 357: 2238-2245. DOI: 10.1002/adsc.201500253 |
0.539 |
|
2014 |
Ma S, Reeves CM, Craig RA, Stoltz BM. Palladium-catalyzed decarboxylative allylic alkylation of diastereomeric β-ketoesters. Tetrahedron. 70: 4208-4212. PMID 24999286 DOI: 10.1016/J.Tet.2014.03.042 |
0.755 |
|
2014 |
Craig RA, O'Connor NR, Goldberg AF, Stoltz BM. Stereoselective Lewis acid mediated (3+2) cycloadditions of N-H- and N-sulfonylaziridines with heterocumulenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 4806-13. PMID 24604740 DOI: 10.1002/Chem.201303699 |
0.663 |
|
2012 |
Craig RA, Roizen JL, Smith RC, Jones AC, Stoltz BM. Enantioselective synthesis of a hydroxymethyl-cis-1,3-cyclopentenediol building block. Organic Letters. 14: 5716-9. PMID 23101616 DOI: 10.1021/Ol3027297 |
0.763 |
|
2012 |
Goldberg AF, O'Connor NR, Craig RA, Stoltz BM. Lewis acid mediated (3 + 2) cycloadditions of donor-acceptor cyclopropanes with heterocumulenes. Organic Letters. 14: 5314-7. PMID 23046060 DOI: 10.1021/Ol302494N |
0.677 |
|
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