| Year |
Citation |
Score |
| 2022 |
Stivala CE, Zbieg JR, Liu P, Krische MJ. Chiral Amines via Enantioselective π-Allyliridium-,-Benzoate-Catalyzed Allylic Alkylation: Student Training via Industrial-Academic Collaboration. Accounts of Chemical Research. PMID 35830564 DOI: 10.1021/acs.accounts.2c00302 |
0.409 |
|
| 2022 |
Jung WO, Yoo M, Migliozzi MM, Zbieg JR, Stivala CE, Krische MJ. Regio- and Enantioselective Iridium-Catalyzed Amination of Alkyl-Substituted Allylic Acetates with Secondary Amines. Organic Letters. 24: 441-445. PMID 34905364 DOI: 10.1021/acs.orglett.1c04135 |
0.399 |
|
| 2021 |
Jung WO, Mai BK, Spinello BJ, Dubey ZJ, Kim SW, Stivala CE, Zbieg JR, Liu P, Krische MJ. Enantioselective Iridium-Catalyzed Allylation of Nitroalkanes: Entry to β-Stereogenic α-Quaternary Primary Amines. Journal of the American Chemical Society. PMID 34152145 DOI: 10.1021/jacs.1c05212 |
0.314 |
|
| 2021 |
Trost BM, Taft BR, Tracy JS, Stivala CE. Catalytic Asymmetric Synthesis of the Pentacyclic Core of (+)-Citrinadin A. Organic Letters. PMID 34114462 DOI: 10.1021/acs.orglett.1c01389 |
0.361 |
|
| 2019 |
Kim SW, Schempp T, Zbieg J, Stivala C, Krische MJ, Kim SW. Regio- and Enantioselective Iridium-Catalyzed N-Allylation of Indoles and Related Azoles with Racemic Branched Alkyl-Substituted Allylic Acetates. Angewandte Chemie (International Ed. in English). PMID 30964961 DOI: 10.1002/Anie.201902799 |
0.391 |
|
| 2018 |
Kim SW, Schwartz LA, Zbieg JR, Stivala CE, Krische MJ. Regio- and Enantioselective Iridium-Catalyzed Amination of Racemic Branched Alkyl-Substituted Allylic Acetates with Primary and Secondary Aromatic and Heteroaromatic Amines. Journal of the American Chemical Society. PMID 30571092 DOI: 10.1021/Jacs.8B12152 |
0.391 |
|
| 2018 |
Trost BM, Bai WJ, Stivala CE, Hohn C, Poock C, Heinrich M, Xu S, Rey J. Enantioselective Synthesis of des-epoxy-Amphidinolide N. Journal of the American Chemical Society. PMID 30457857 DOI: 10.1021/Jacs.8B11827 |
0.361 |
|
| 2018 |
Kim SW, Wurm T, Brito GA, Jung WO, Zbieg JR, Stivala CE, Krische MJ. Hydroamination versus Allylic Amination in Iridium-Catalyzed Reactions of Allylic Acetates with Amines: 1,3-Aminoalcohols via Ester-Directed Regioselectivity. Journal of the American Chemical Society. PMID 29989803 DOI: 10.1021/Jacs.8B05683 |
0.436 |
|
| 2018 |
Meza AT, Wurm T, Smith L, Kim SW, Zbieg JR, Stivala CE, Krische MJ. Amphiphilic π-Allyliridium C,O-Benzoates Enable Regio- and Enantioselective Amination of Branched Allylic Acetates Bearing Linear Alkyl Groups. Journal of the American Chemical Society. PMID 29350523 DOI: 10.1021/Jacs.7B13482 |
0.446 |
|
| 2018 |
Daniels BE, Stivala CE. A solid-phase approach for the synthesis of α-aminoboronic acid peptides Rsc Advances. 8: 3343-3347. DOI: 10.1039/C7Ra13479G |
0.319 |
|
| 2017 |
Schempp TT, Daniels BE, Staben ST, Stivala CE. A General Strategy for the Construction of Functionalized Azaindolines via Domino Palladium-Catalyzed Heck Cyclization/Suzuki Coupling. Organic Letters. PMID 28653542 DOI: 10.1021/Acs.Orglett.7B01606 |
0.458 |
|
| 2016 |
Yu K, Lu P, Jackson JJ, Nguyen TD, Alvarado J, Stivala CE, Ma Y, Mack KA, Hayton TW, Collum DB, Zakarian A. Lithium Enolates in the Enantioselective Construction of Tetrasubstituted Carbon Centers with Chiral Lithium Amides as Noncovalent Stereodirecting Auxiliaries. Journal of the American Chemical Society. PMID 27997174 DOI: 10.1021/Jacs.6B11673 |
0.666 |
|
| 2016 |
Trost BM, Stivala CE, Fandrick DR, Hull KL, Huang A, Poock C, Kalkofen R. Total Synthesis of (-)-Lasonolide A. Journal of the American Chemical Society. PMID 27548113 DOI: 10.1021/Jacs.6B05127 |
0.462 |
|
| 2015 |
Stivala CE, Benoit E, Aráoz R, Servent D, Novikov A, Molgó J, Zakarian A. Synthesis and biology of cyclic imine toxins, an emerging class of potent, globally distributed marine toxins. Natural Product Reports. 32: 411-35. PMID 25338021 DOI: 10.1039/C4Np00089G |
0.545 |
|
| 2014 |
Trost BM, Stivala CE, Hull KL, Huang A, Fandrick DR. A concise synthesis of (-)-lasonolide A. Journal of the American Chemical Society. 136: 88-91. PMID 24308383 DOI: 10.1021/Ja411270D |
0.469 |
|
| 2014 |
Carreira EM, Jacobsen MJ, Trost BM, Stivala CE, Hull KL, Huang A, Fandrick DR. Synthesis of (–)-Lasonolide A Synfacts. 10: 235-235. DOI: 10.1055/S-0033-1340711 |
0.414 |
|
| 2014 |
Trost BM, Stivala CE, Hull KL, Huang A, Fandrick DR. ChemInform Abstract: A Concise Synthesis of (-)-Lasonolide A (I). Cheminform. 45: no-no. DOI: 10.1002/chin.201430217 |
0.366 |
|
| 2013 |
Ma Y, Stivala CE, Wright AM, Hayton T, Liang J, Keresztes I, Lobkovsky E, Collum DB, Zakarian A. Enediolate-dilithium amide mixed aggregates in the enantioselective alkylation of arylacetic acids: structural studies and a stereochemical model. Journal of the American Chemical Society. 135: 16853-64. PMID 23654300 DOI: 10.1021/Ja403076U |
0.584 |
|
| 2012 |
Jackson JJ, Stivala CE, Iorga BI, Molgó J, Zakarian A. Stability of cyclic imine toxins: interconversion of pinnatoxin amino ketone and pinnatoxin A in aqueous media. The Journal of Organic Chemistry. 77: 10435-40. PMID 23116445 DOI: 10.1021/Jo301632D |
0.624 |
|
| 2012 |
Stivala CE, Gu Z, Smith LL, Zakarian A. Studies toward the synthesis of spirolide C: exploration into the formation of the 23-membered all-carbon macrocyclic framework. Organic Letters. 14: 804-7. PMID 22260643 DOI: 10.1021/Ol203342E |
0.648 |
|
| 2011 |
Stivala CE, Zakarian A. Highly enantioselective direct alkylation of arylacetic acids with chiral lithium amides as traceless auxiliaries. Journal of the American Chemical Society. 133: 11936-9. PMID 21744818 DOI: 10.1021/Ja205107X |
0.641 |
|
| 2011 |
Araoz R, Servent D, Molgoí J, Iorga BI, Fruchart-Gaillard C, Benoit E, Gu Z, Stivala C, Zakarian A. Total synthesis of pinnatoxins A and G and revision of the mode of action of pinnatoxin A Journal of the American Chemical Society. 133: 10499-10511. PMID 21644584 DOI: 10.1021/Ja201254C |
0.614 |
|
| 2010 |
Herrmann AT, Saito T, Stivala CE, Tom J, Zakarian A. Regio- and stereocontrol in rhenium-catalyzed transposition of allylic alcohols. Journal of the American Chemical Society. 132: 5962-3. PMID 20387811 DOI: 10.1021/Ja101673V |
0.726 |
|
| 2010 |
Herrmann AT, Saito T, Stivala CE, Tom J, Zakarian A. Synthesis of 1,3-syn-Diol Acetalsvia Re-Catalyzed Allylic Alcohol Transposition Synfacts. 2010: 915-915. DOI: 10.1055/S-0030-1257819 |
0.634 |
|
| 2010 |
Gu Z, Herrmann AT, Stivala CE, Zakarian A. Stereoselective construction of adjacent quaternary chiral centers by the Ireland-Claisen rearrangement: Stereoselection with esters of cyclic alcohols Synlett. 1717-1722. DOI: 10.1055/S-0029-1219965 |
0.654 |
|
| 2009 |
Ilardi EA, Stivala CE, Zakarian A. [3,3]-Sigmatropic rearrangements: recent applications in the total synthesis of natural products. Chemical Society Reviews. 38: 3133-48. PMID 19847347 DOI: 10.1039/B901177N |
0.703 |
|
| 2009 |
Stivala CE, Zakarian A. Studies toward the synthesis of spirolides: assembly of the elaborated E-ring fragment. Organic Letters. 11: 839-42. PMID 19199776 DOI: 10.1021/Ol8027797 |
0.616 |
|
| 2008 |
Ilardi EA, Stivala CE, Zakarian A. Hexafluoroisopropanol as a unique solvent for stereoselective iododesilylation of vinylsilanes. Organic Letters. 10: 1727-30. PMID 18386904 DOI: 10.1021/Ol800341Z |
0.7 |
|
| 2008 |
Stivala CE, Zakarian A. Total synthesis of (+)-pinnatoxin A. Journal of the American Chemical Society. 130: 3774-6. PMID 18311987 DOI: 10.1021/Ja800435J |
0.665 |
|
| 2008 |
Stivala CE, Zakarian A. Synthesis of (+)-Pinnatoxin A Synfacts. 2008: 782-782. DOI: 10.1055/S-2008-1078529 |
0.644 |
|
| 2007 |
Qin YC, Stivala CE, Zakarian A. Acyclic stereocontrol in the Ireland-Claisen rearrangement of alpha-branched esters. Angewandte Chemie (International Ed. in English). 46: 7466-9. PMID 17694517 DOI: 10.1002/Anie.200702142 |
0.538 |
|
| 2007 |
Stivala CE, Zakarian A. Studies toward the synthesis of pinnatoxins: the spiroimine fragment Tetrahedron Letters. 48: 6845-6848. DOI: 10.1016/J.Tetlet.2007.07.182 |
0.651 |
|
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