| Year |
Citation |
Score |
| 2024 |
Trofimova DN, Aeluri M, Veeranna KD, Jiang Y, Grange RL, Pipaliya BV, Subaramanian M, Craig AW, Evans PA, Allingham JS. Toward a Template for Synthetic Actin-Targeting Macrolide Analogues That Inhibit Cancer Cell Invasiveness. Journal of Medicinal Chemistry. PMID 38401158 DOI: 10.1021/acs.jmedchem.3c01532 |
0.696 |
|
| 2023 |
Ylagan RMP, Lee EJ, Negru DE, Ricci P, Park B, Ryu H, Baik MH, Evans PA. Enantioselective Rhodium-Catalyzed Pauson-Khand Reactions of 1,6-Chloroenynes with 1,1-Disubstituted Olefins. Angewandte Chemie (International Ed. in English). e202300211. PMID 36893215 DOI: 10.1002/anie.202300211 |
0.322 |
|
| 2023 |
Zhu Y, Zheng J, Evans PA. Intramolecular Rhodium-Catalyzed [(3+2+2)] Carbocyclization Reactions with Dienylidenecyclopropanes: A Concise and Stereoselective Total Synthesis of the Sesquiterpene (+)-Zizaene. Journal of the American Chemical Society. PMID 36745821 DOI: 10.1021/jacs.2c10923 |
0.37 |
|
| 2021 |
Pipaliya BV, Trofimova DN, Grange RL, Aeluri M, Deng X, Shah K, Craig AW, Allingham JS, Evans PA. Truncated Actin-Targeting Macrolide Derivative Blocks Cancer Cell Motility and Invasion of Extracellular Matrix. Journal of the American Chemical Society. PMID 33938740 DOI: 10.1021/jacs.0c12404 |
0.684 |
|
| 2020 |
Pal D, Wright TB, O'Connor R, Evans PA. Regio- and Diastereoselective Rhodium-Catalyzed Allylic Substitution with Unstabilized Benzyl Nucleophiles. Angewandte Chemie (International Ed. in English). PMID 32840011 DOI: 10.1002/anie.202008071 |
0.334 |
|
| 2020 |
Tom MJ, Evans PA. Regioselective and Stereospecific Rhodium-Catalyzed Allylic Cyanomethylation with an Acetonitrile Equivalent: Construction of Acyclic β-Quaternary Stereogenic Nitriles. Journal of the American Chemical Society. PMID 32486634 DOI: 10.1021/Jacs.0C02316 |
0.431 |
|
| 2020 |
Pal D, Wright TB, O’Connor R, Evans PA. Regio- and Diastereoselective Rhodium-Catalyzed Allylic Substitution with Unstabilized Benzyl Nucleophiles. Angewandte Chemie. DOI: 10.1002/Ange.202008071 |
0.44 |
|
| 2019 |
Majhi J, Turnbull BWH, Ryu H, Park J, Baik MH, Evans PA. Dynamic Kinetic Resolution of Alkenyl Cyanohydrins Derived from α,β-Unsaturated Aldehydes: Stereoselective Synthesis of E-Tetrasubstituted Olefins. Journal of the American Chemical Society. PMID 31180679 DOI: 10.1021/Jacs.9B04384 |
0.4 |
|
| 2019 |
Wright TB, Turnbull BWH, Evans PA. Enantioselective Rhodium-Catalyzed Allylic Alkylation of β,γ-Unsaturated α-Amino Nitriles: Synthetic Homoenolate Equivalents. Angewandte Chemie (International Ed. in English). PMID 30957357 DOI: 10.1002/Anie.201900442 |
0.386 |
|
| 2017 |
Su Y, Inglesby PA, Evans PA. Intramolecular Thioether Migration in the Rhodium-Catalyzed Ene-Cycloisomerization of Alkenylidenecyclopropanes via a Metal-Mediated β-Sulfide Elimination. Angewandte Chemie (International Ed. in English). PMID 29065243 DOI: 10.1002/Anie.201709059 |
0.377 |
|
| 2017 |
Turnbull BWH, Chae J, Oliver S, Evans PA. Regio- and stereospecific rhodium-catalyzed allylic alkylation with an acyl anion equivalent: an approach to acyclic α-ternary β,γ-unsaturated aryl ketones. Chemical Science. 8: 4001-4005. PMID 28553542 DOI: 10.1039/C6Sc05705E |
0.399 |
|
| 2017 |
Chen D, Evans PA. A Concise, Efficient and Scalable Total Synthesis of Thapsigargin and Nortrilobolide from (R)-(-)-Carvone. Journal of the American Chemical Society. PMID 28422492 DOI: 10.1021/Jacs.7B01734 |
0.372 |
|
| 2016 |
Wright TB, Evans PA. Enantioselective Rhodium-Catalyzed Allylic Alkylation of Prochiral α,α-Disubstituted Aldehyde Enolates for the Construction of Acyclic Quaternary Stereogenic Centers. Journal of the American Chemical Society. 138: 15303-15306. PMID 27933923 DOI: 10.1021/Jacs.6B10099 |
0.407 |
|
| 2016 |
Evans PA, Čusak A, Grisin A, Lawler MJ, Pink M. Medium-Ring Stereocontrol in the Temporary Silicon-Tethered Ring-Closing Metathesis Approach to the Synthesis of Polyketide Fragments Synthesis (Germany). 48: 2402-2412. DOI: 10.1055/S-0035-1562094 |
0.384 |
|
| 2016 |
Grange RL, Clizbe EA, Evans PA. Recent Developments in Asymmetric Allylic Amination Reactions Synthesis. 48: 2911-2968. DOI: 10.1055/S-0035-1562090 |
0.412 |
|
| 2015 |
Grange RL, Clizbe EA, Counsell EJ, Evans PA. Enantioselective construction of C-chiral allylic sulfilimines via the iridium-catalyzed allylic amination with S,S-diphenylsulfilimine: asymmetric synthesis of primary allylic amines. Chemical Science. 6: 777-781. PMID 28936319 DOI: 10.1039/c4sc01317d |
0.307 |
|
| 2015 |
Crandell DW, Mazumder S, Evans PA, Baik MH. The origin of the ligand-controlled regioselectivity in Rh-catalyzed [(2 + 2) + 2] carbocyclizations: steric vs. stereoelectronic effects. Chemical Science. 6: 6896-6900. PMID 28757978 DOI: 10.1039/C5Sc02307F |
0.319 |
|
| 2015 |
Grisin A, Evans PA. A highly convergent synthesis of the C1-C31 polyol domain of amphidinol 3 featuring a TST-RCM reaction: confirmation of the revised relative stereochemistry. Chemical Science. 6: 6407-6412. PMID 28757956 DOI: 10.1039/C5Sc00814J |
0.348 |
|
| 2015 |
Krauthammer M, Kong Y, Bacchiocchi A, Evans P, Pornputtapong N, Wu C, McCusker JP, Ma S, Cheng E, Straub R, Serin M, Bosenberg M, Ariyan S, Narayan D, Sznol M, et al. Exome sequencing identifies recurrent mutations in NF1 and RASopathy genes in sun-exposed melanomas. Nature Genetics. PMID 26214590 DOI: 10.1038/Ng.3361 |
0.494 |
|
| 2015 |
Turnbull BW, Evans PA. Enantioselective rhodium-catalyzed allylic substitution with a nitrile anion: construction of acyclic quaternary carbon stereogenic centers. Journal of the American Chemical Society. 137: 6156-9. PMID 25941763 DOI: 10.1021/Jacs.5B02810 |
0.471 |
|
| 2015 |
Evans PA, Negru DE, Shang D. Rhodium-catalyzed [(3+2)+2] carbocyclization of alkynylidenecyclopropanes with substituted allenes: stereoselective construction of tri- and tetrasubstituted exocyclic olefins. Angewandte Chemie (International Ed. in English). 54: 4768-72. PMID 25728537 DOI: 10.1002/Anie.201410857 |
0.465 |
|
| 2014 |
Evans PA, Burnie AJ, Negru DE. Rhodium-catalyzed [(3+2)+1] carbocyclization reactions of alkynylidenecyclopropanes with carbon monoxide: regiospecific construction of polysubstituted phenols. Organic Letters. 16: 4356-9. PMID 25111872 DOI: 10.1021/ol501724s |
0.31 |
|
| 2014 |
Grange RL, Evans PA. Metal-free metathesis reaction of C-chiral allylic sulfilimines with aryl isocyanates: construction of chiral nonracemic allylic isocyanates. Journal of the American Chemical Society. 136: 11870-3. PMID 25109231 DOI: 10.1021/Ja504631V |
0.423 |
|
| 2014 |
Inglesby PA, Bacsa J, Negru DE, Evans PA. The isolation and characterization of a rhodacycle intermediate implicated in metal-catalyzed reactions of alkylidenecyclopropanes. Angewandte Chemie (International Ed. in English). 53: 3952-6. PMID 24616050 DOI: 10.1002/Anie.201310232 |
0.399 |
|
| 2014 |
Ojo OS, Inglesby PA, Negru DE, Evans PA. A convenient, economical and scalable multi-gram synthesis of 1-vinylcyclopropyl 4-methylbenzenesulfonate Organic Chemistry Frontiers. 1: 821-824. DOI: 10.1039/C4Qo00089G |
0.358 |
|
| 2013 |
Evans PA, Oliver S. Regio- and enantiospecific rhodium-catalyzed allylic substitution with an acyl anion equivalent. Organic Letters. 15: 5626-9. PMID 24180456 DOI: 10.1021/ol402336u |
0.381 |
|
| 2013 |
Evans PA, Inglesby PA, Kilbride K. A concise total synthesis of pyrovellerolactone using a rhodium-catalyzed [(3 + 2) + 2] carbocyclization reaction. Organic Letters. 15: 1798-801. PMID 23540706 DOI: 10.1021/Ol400165X |
0.471 |
|
| 2013 |
Oliver S, Evans PA. Transition-metal-catalyzed allylic substitution reactions: Stereoselective construction of α- And β-substituted carbonyl compounds Synthesis (Germany). 45: 3179-3198. DOI: 10.1055/S-0033-1338538 |
0.412 |
|
| 2013 |
Evans PA, Baikstis T, Inglesby PA. Stereoselective rhodium-catalyzed [(3+2)+2] carbocyclization reaction of trialkoxysilyl-substituted alkenylidenecyclopropanes with monosubstituted alkynes Tetrahedron. 69: 7826-7830. DOI: 10.1016/J.Tet.2013.05.096 |
0.426 |
|
| 2012 |
Evans PA, Oliver S, Chae J. Rhodium-catalyzed allylic substitution with an acyl anion equivalent: stereospecific construction of acyclic quaternary carbon stereogenic centers. Journal of the American Chemical Society. 134: 19314-7. PMID 23157367 DOI: 10.1021/Ja306602G |
0.478 |
|
| 2012 |
Mazumder S, Shang D, Negru DE, Baik MH, Evans PA. Stereoselective rhodium-catalyzed [3 + 2 + 1] carbocyclization of alkenylidenecyclopropanes with carbon monoxide: theoretical evidence for a trimethylenemethane metallacycle intermediate. Journal of the American Chemical Society. 134: 20569-72. PMID 22928792 DOI: 10.1021/Ja305467X |
0.394 |
|
| 2012 |
Evans PA, Huang MH, Lawler MJ, Maroto S. Total synthesis of marinomycin A using salicylate as a molecular switch to mediate dimerization. Nature Chemistry. 4: 680-4. PMID 22824902 DOI: 10.1038/Nchem.1330 |
0.314 |
|
| 2012 |
Evans PA, Inglesby PA. Diastereoselective rhodium-catalyzed ene-cycloisomerization reactions of alkenylidenecyclopropanes: total synthesis of (-)-α-kainic acid. Journal of the American Chemical Society. 134: 3635-8. PMID 22335403 DOI: 10.1021/Ja210804R |
0.446 |
|
| 2012 |
Evans PA, Grisin A, Lawler MJ. Diastereoselective construction of syn-1,3-dioxanes via a bismuth-mediated two-component hemiacetal/oxa-conjugate addition reaction. Journal of the American Chemical Society. 134: 2856-9. PMID 22296255 DOI: 10.1021/Ja208668U |
0.402 |
|
| 2012 |
Evans PA, Clizbe EA, Lawler MJ, Oliver S. Enantioselective rhodium-catalyzed allylic alkylation of acyclic α-alkoxy substituted ketones using a chiral monodentate phosphite ligand Chemical Science. 3: 1835-1838. DOI: 10.1039/C2Sc20141K |
0.411 |
|
| 2011 |
Baik MH, Mazumder S, Ricci P, Sawyer JR, Song YG, Wang H, Evans PA. Computationally designed and experimentally confirmed diastereoselective rhodium-catalyzed Pauson-Khand reaction at room temperature. Journal of the American Chemical Society. 133: 7621-3. PMID 21524123 DOI: 10.1021/Ja107895G |
0.328 |
|
| 2010 |
Evans PA, Sawyer JR, Inglesby PA. Regiodivergent ligand-controlled rhodium-catalyzed [(2+2)+2] carbocyclization reactions with alkyl substituted methyl propiolates. Angewandte Chemie (International Ed. in English). 49: 5746-9. PMID 20629057 DOI: 10.1002/Anie.201002117 |
0.411 |
|
| 2010 |
Inglesby PA, Evans PA. Stereoselective transition metal-catalysed higher-order carbocyclisation reactions. Chemical Society Reviews. 39: 2791-805. PMID 20505862 DOI: 10.1039/B913110H |
0.315 |
|
| 2010 |
EVANS PA, HOLMES AB, MCGEARY RP, NADIN A, RUSSELL K, O'HANLON PJ, PEARSON ND. ChemInform Abstract: New Methodology for the Synthesis of Unsaturated 8-, 9-, and 10- Membered Lactams. Cheminform. 27: no-no. DOI: 10.1002/chin.199619187 |
0.477 |
|
| 2010 |
EVANS PA, HOLMES AB, COLLINS I, RAITHBY PR, RUSSELL K. ChemInform Abstract: The First Example of a Transoid Amide (Imide) in an Eight-Membered Lactam. Cheminform. 27: no-no. DOI: 10.1002/chin.199613178 |
0.425 |
|
| 2010 |
EVANS PA, HOLMES AB, RUSSELL K. ChemInform Abstract: New Synthetic Methodology for the Synthesis of 7-Substituted Tetrahydroazepin-2-ones. Cheminform. 26: no-no. DOI: 10.1002/chin.199520148 |
0.498 |
|
| 2009 |
Evans PA, Clizbe EA. Unlocking ylide reactivity in the metal-catalyzed allylic substitution reaction: stereospecific construction of primary allylic amines with aza-ylides. Journal of the American Chemical Society. 131: 8722-3. PMID 19499919 DOI: 10.1021/Ja9041302 |
0.442 |
|
| 2008 |
Evans PA, Inglesby PA. Intermolecular rhodium-catalyzed [3+2+2] carbocyclization of alkenylidenecyclopropanes with activated alkynes: regio- and diastereoselective construction of cis-fused bicycloheptadienes. Journal of the American Chemical Society. 130: 12838-9. PMID 18778054 DOI: 10.1021/Ja803691P |
0.409 |
|
| 2008 |
Evans PA, Andrews WJ. A sequential two-component etherification/oxa-conjugate addition reaction: asymmetric synthesis of (+)-leucascandrolide A macrolactone. Angewandte Chemie (International Ed. in English). 47: 5426-9. PMID 18551691 DOI: 10.1002/Anie.200801357 |
0.439 |
|
| 2008 |
Wang H, Sawyer JR, Evans PA, Baik MH. Mechanistic insight into the diastereoselective rhodium-catalyzed Pauson-Khand reaction: role of coordination number in stereocontrol. Angewandte Chemie (International Ed. in English). 47: 342-5. PMID 18022985 DOI: 10.1002/Anie.200702822 |
0.361 |
|
| 2007 |
Evans PA, Qin J, Robinson JE, Bazin B. Enantioselective total synthesis of the polycyclic guanidine-containing marine alkaloid (-)-batzelladine D. Angewandte Chemie (International Ed. in English). 46: 7417-9. PMID 17763494 DOI: 10.1002/Anie.200700840 |
0.348 |
|
| 2006 |
Evans PA, Lawler MJ. Rhodium-catalyzed propargylic substitution: a divergent approach to propargylic and allenyl sulfonamides. Angewandte Chemie (International Ed. in English). 45: 4970-2. PMID 16819738 DOI: 10.1002/Anie.200600615 |
0.382 |
|
| 2006 |
Evans PA, Lai KW, Zhang HR, Huffman JC. Regioselective and enantiospecific rhodium-catalyzed allylic amination with thymine: synthesis of a new conformationally rigid nucleoside. Chemical Communications (Cambridge, England). 844-6. PMID 16479286 DOI: 10.1039/B513083B |
0.434 |
|
| 2006 |
Alexander MD, Burkart MD, Leonard MS, Portonovo P, Liang B, Ding X, Joullié MM, Gulledge BM, Aggen JB, Chamberlin AR, Sandler J, Fenical W, Cui J, Gharpure SJ, Polosukhin A, ... ... Evans PA, et al. A central strategy for converting natural products into fluorescent probes. Chembiochem : a European Journal of Chemical Biology. 7: 409-16. PMID 16432909 DOI: 10.1002/Cbic.200500466 |
0.544 |
|
| 2006 |
Evans PA, Baum EW, Fazal AN, Lai KW, Robinson JE, Sawyer JR. New metal-catalyzed carbocyclization reactions for the construction of complex natural products Arkivoc. 2006: 338-358. DOI: 10.3998/Ark.5550190.0007.725 |
0.43 |
|
| 2005 |
Evans PA, Andrews WJ. Stereoselective construction of cis-2,6-disubstituted tetrahydropyrans via an intramolecular bismuth-mediated oxa-conjugate addition reaction. Tetrahedron Letters. 46: 5625-5627. PMID 16710442 DOI: 10.1016/J.Tetlet.2005.06.100 |
0.395 |
|
| 2005 |
Evans PA, Lai KW, Sawyer JR. Regio- and enantioselective intermolecular rhodium-catalyzed [2+2+2] carbocyclization reactions of 1,6-enynes with methyl arylpropiolates. Journal of the American Chemical Society. 127: 12466-7. PMID 16144375 DOI: 10.1021/Ja053123Y |
0.452 |
|
| 2005 |
Evans PA, Sawyer JR, Lai KW, Huffman JC. Intermolecular rhodium-catalyzed [2+2+2] carbocyclization reactions of 1,6-enynes with symmetrical and unsymmetrical alkynes. Chemical Communications (Cambridge, England). 3971-3. PMID 16075089 DOI: 10.1039/B505383H |
0.431 |
|
| 2005 |
Baik MH, Baum EW, Burland MC, Evans PA. Diastereoselective intermolecular rhodium-catalyzed [4 + 2 + 2] carbocyclization reactions: computational and experimental evidence for the intermediacy of an alternative metallacycle intermediate. Journal of the American Chemical Society. 127: 1602-3. PMID 15700970 DOI: 10.1021/Ja043521L |
0.42 |
|
| 2005 |
Evans PA, Baum EW, Fazal AN, Pink M. Diastereoselective metal-catalyzed [4 + 2 + 2] carbocyclization reactions utilizing a rhodium N-heterocyclic carbene (NHC) complex: the first example of a rhodium NHC-catalyzed [m + n + o] carbocyclization. Chemical Communications (Cambridge, England). 63-5. PMID 15614373 DOI: 10.1039/B413438A |
0.309 |
|
| 2005 |
Leahy DK, Evans PA. Rhodium(I)-Catalyzed Allylic Substitution Reactions and Their Applications to Target Directed Synthesis Modern Rhodium-Catalyzed Organic Reactions. 191-214. DOI: 10.1002/3527604693.ch10 |
0.308 |
|
| 2004 |
Evans PA, Leahy DK, Andrews WJ, Uraguchi D. Stereodivergent construction of cyclic ethers by a regioselective and enantiospecific rhodium-catalyzed allylic etherification: total synthesis of gaur acid. Angewandte Chemie (International Ed. in English). 43: 4788-91. PMID 15366088 DOI: 10.1002/Anie.200460612 |
0.417 |
|
| 2004 |
Evans PA, Baum EW. Diastereoselective intramolecular temporary silicon-tethered rhodium-catalyzed [4+2+2] cycloisomerization reactions: regiospecific incorporation of substituted 1,3-butadienes. Journal of the American Chemical Society. 126: 11150-1. PMID 15355086 DOI: 10.1021/Ja046030+ |
0.461 |
|
| 2004 |
Evans PA, Lawler MJ. Regio- and diastereoselective rhodium-catalyzed allylic substitution with acyclic alpha-alkoxy-substituted copper(I) enolates: stereodivergent approach to 2,3,6-trisubstituted dihydropyrans. Journal of the American Chemical Society. 126: 8642-3. PMID 15250703 DOI: 10.1021/Ja049080N |
0.442 |
|
| 2003 |
Evans PA, Leahy DK. Recent Developments in Rhodium-Catalyzed Allylic Substitution and Carbocyclization Reactions. Chemtracts. 16: 567-578. PMID 17047733 |
0.335 |
|
| 2003 |
Evans PA, Leahy DK. Regioselective and enantiospecific rhodium-catalyzed allylic alkylation reactions using copper(I) enolates: synthesis of (-)-sugiresinol dimethyl ether. Journal of the American Chemical Society. 125: 8974-5. PMID 15369328 DOI: 10.1021/Ja035983P |
0.469 |
|
| 2003 |
Evans PA, Cui J, Gharpure SJ, Polosukhin A, Zhang HR. Enantioselective total synthesis of the potent antitumor agent (-)-mucocin using a temporary silicon-tethered ring-closing metathesis cross-coupling reaction. Journal of the American Chemical Society. 125: 14702-3. PMID 14640634 DOI: 10.1021/Ja0384734 |
0.672 |
|
| 2003 |
Evans PA, Cui J, Gharpure SJ. Stereoselective construction of cis-2,6-disubstituted tetrahydropyrans via the reductive etherification of delta-trialkylsilyloxy substituted ketones: total synthesis of (-)-centrolobine. Organic Letters. 5: 3883-5. PMID 14535734 DOI: 10.1021/Ol035438T |
0.66 |
|
| 2003 |
Evans PA, Cui J, Gharpure SJ, Hinkle RJ. Stereoselective construction of cyclic ethers using a tandem two-component etherification: elucidation of the role of bismuth tribromide. Journal of the American Chemical Society. 125: 11456-7. PMID 13129322 DOI: 10.1021/Ja036439J |
0.676 |
|
| 2003 |
Evans PA, Uraguchi D. Regio- and enantiospecific rhodium-catalyzed arylation of unsymmetrical fluorinated acyclic allylic carbonates: inversion of absolute configuration. Journal of the American Chemical Society. 125: 7158-9. PMID 12797772 DOI: 10.1021/Ja035216Q |
0.439 |
|
| 2003 |
Evans PA, Cui J, Buffone GP. Diastereoselective temporary silicon-tethered ring-closing-metathesis reactions with prochiral alcohols: a new approach to long-range asymmetric induction. Angewandte Chemie (International Ed. in English). 42: 1734-7. PMID 12707892 DOI: 10.1002/Anie.200250486 |
0.34 |
|
| 2003 |
Evans PA, Robinson JE, Baum aEW, Fazal AN. Intermolecular Transition Metal-Catalyzed [4 + 2 + 2] Cycloaddition Reactions: A New Approach to the Construction of Eight-Membered Rings [J. Am. Chem. Soc. 2002, 124 (30), 8782−8783]. Journal of the American Chemical Society. 125: 14648-14648. DOI: 10.1021/Ja033458K |
0.369 |
|
| 2003 |
Evans PA, Leahy DK, Slieker LM. Halide ion effects in the rhodium-catalyzed allylic substitution reaction using copper(I) alkoxides and enolates Tetrahedron Asymmetry. 14: 3613-3618. DOI: 10.1016/J.Tetasy.2003.08.044 |
0.346 |
|
| 2003 |
Evans PA, Cui J, Buffone GP. Cover Picture: Diastereoselective Temporary Silicon-Tethered Ring-Closing-Metathesis Reactions with Prochiral Alcohols: A New Approach to Long-Range Asymmetric Induction (Angew. Chem. Int. Ed. 15/2003) Angewandte Chemie International Edition. 42: 1671-1671. DOI: 10.1002/Anie.200390379 |
0.341 |
|
| 2003 |
Nelson JD, Modi DP, Evans PA. Photo‐Induced Ring Expansion of 1‐Triisopropylsilyloxy‐1‐Azidocyclohexane: Preparation of ε‐Caprolactam Organic Syntheses. 79: 165-165. DOI: 10.1002/0471264180.Os079.20 |
0.347 |
|
| 2002 |
Evans PA, Robinson JE, Baum EW, Fazal AN. Intermolecular transition metal-catalyzed [4 + 2 + 2] cycloaddition reactions: a new approach to the construction of eight-membered rings. Journal of the American Chemical Society. 124: 8782-3. PMID 12137516 DOI: 10.1021/Ja026351Q |
0.417 |
|
| 2002 |
Evans PA, Leahy DK. Regio- and enantiospecific rhodium-catalyzed allylic etherification reactions using copper(I) alkoxides: influence of the copper halide salt on selectivity. Journal of the American Chemical Society. 124: 7882-3. PMID 12095315 DOI: 10.1021/Ja026337D |
0.379 |
|
| 2001 |
Evans PA, Raina S, Ahsan K. Intramolecular addition of acyl radicals to alpha-substituted vinylogous carbonates: demonstrating the effect of ring size on acyclic stereocontrol. Chemical Communications (Cambridge, England). 2504-5. PMID 12240036 DOI: 10.1039/B106766B |
0.332 |
|
| 2001 |
Evans PA, Robinson JE, Moffett KK. Regioselective and enantiospecific rhodium-catalyzed allylic amination with N-(arylsulfonyl)anilines. Organic Letters. 3: 3269-71. PMID 11594811 DOI: 10.1021/ol016467b |
0.302 |
|
| 2001 |
Evans PA, Robinson JE. Regio- and diastereoselective tandem rhodium-catalyzed allylic alkylation/Pauson-Khand annulation reactions. Journal of the American Chemical Society. 123: 4609-10. PMID 11457251 DOI: 10.1021/ja015531h |
0.305 |
|
| 2001 |
Evans PA, Kennedy LJ. Regioselective rhodium-catalyzed allylic alkylation/ring-closing metathesis approach to carbocycles Tetrahedron Letters. 42: 7015-7018. DOI: 10.1016/S0040-4039(01)01467-8 |
0.398 |
|
| 2001 |
Evans PA, Manangan T. Stereoselective construction of the azabicyclic core applicable to the biologically important polyguanidinium alkaloids batzelladine A and D using a free radical cyclization Tetrahedron Letters. 42: 6637-6640. DOI: 10.1016/S0040-4039(01)01340-5 |
0.323 |
|
| 1999 |
Evans PA, Murthy VS, Roseman JD, Rheingold AL. Enantioselective Total Synthesis of the Nonisoprenoid Sesquiterpene (-)-Kumausallene. Angewandte Chemie (International Ed. in English). 38: 3175-3177. PMID 10556893 DOI: 10.1002/(Sici)1521-3773(19991102)38:21<3175::Aid-Anie3175>3.0.Co;2-M |
0.383 |
|
| 1999 |
Evans PA, Robinson aJE, Nelson JD. Enantiospecific Synthesis of Allylamines via the Regioselective Rhodium-Catalyzed Allylic Amination Reaction [J. Am. Chem. Soc. 1999, 121, 6761−6762]. Journal of the American Chemical Society. 121: 12214-12214. DOI: 10.1021/Ja995539F |
0.422 |
|
| 1999 |
Evans PA, Robinson JE, Nelson JD. Enantiospecific synthesis of allylamines via the regioselective rhodium- catalyzed allylic amination reaction [8] Journal of the American Chemical Society. 121: 6761-6762. DOI: 10.1021/Ja991089F |
0.433 |
|
| 1999 |
Evans PA, Brandt TA, Robinson JE. Palladium-catalyzed rearrangement and substitution reactions of acyclic vinylogous carbonates and sulfonates: Development of a new leaving group for Pd-allyl chemistry Tetrahedron Letters. 40: 3105-3108. DOI: 10.1016/S0040-4039(99)00475-X |
0.404 |
|
| 1998 |
Evans PA, Murthy VS. Temporary Silicon-Tethered Ring-Closing Metathesis Approach to C(2)-Symmetrical 1,4-Diols: Asymmetric Synthesis of D-Altritol. The Journal of Organic Chemistry. 63: 6768-6769. PMID 11672287 DOI: 10.1021/Jo9811524 |
0.33 |
|
| 1998 |
Evans PA, Murthy VS. Enantioselective synthesis of the 4-hydroxy buteneolide terminus of mucocin and related annonaceous acetogenins Tetrahedron Letters. 39: 9627-9628. DOI: 10.1016/S0040-4039(98)02206-0 |
0.421 |
|
| 1998 |
Evans PA, Nelson JD. Regioselective rhodium-catalyzed allylic alkylation with a modified Wilkinson's catalyst Tetrahedron Letters. 39: 1725-1728. DOI: 10.1016/S0040-4039(98)00142-7 |
0.321 |
|
| 1997 |
Evans PA, Nelson JD, Manangan T. Preparation and Palladium Mediated Cross-Coupling Reactions of cis-2,3-Disubstituted 5-Halo-Dihydropyran-4-ones Synlett. 1997: 968-970. DOI: 10.1055/S-1997-958 |
0.352 |
|
| 1997 |
Evans PA, Manangan T. Vinylogous sulfonates as radical acceptors for the stereoselective synthesis of cyclic ethers Tetrahedron Letters. 38: 8165-8168. DOI: 10.1016/S0040-4039(97)10248-9 |
0.32 |
|
| 1997 |
Evans PA, Roseman JD. Stereoselective synthesis of the 2,6-disubstituted tetrahydropyran-3-ol of the potent antitumor agent mucocin via an acyl radical cyclization Tetrahedron Letters. 38: 5249-5252. DOI: 10.1016/S0040-4039(97)01147-7 |
0.374 |
|
| 1997 |
Evans PA, Nelson JD, Rheingold AL. Novel Wagner-Meerwein rearrangement of a bicyclo[3.1.1]heptanol under Mitsunobu conditions Tetrahedron Letters. 38: 2235-2236. DOI: 10.1016/S0040-4039(97)00325-0 |
0.303 |
|
| 1996 |
Evans PA, Nelson JD. Stereoselective Synthesis of Dihydropyran-4-ones via a Formal Hetero Diels-Alder Reaction and Ceric Ammonium Nitrate Dehydrogenation. The Journal of Organic Chemistry. 61: 7600-7602. PMID 11667695 |
0.307 |
|
| 1996 |
Evans PA, Holmes AB, McGeary RP, Nadin A, Russell K, O'Hanlon PJ, Pearson ND. New methodology for the synthesis of unsaturated 8-, 9- and 10-membered lactams Journal of the Chemical Society-Perkin Transactions 1. 123-138. DOI: 10.1039/P19960000123 |
0.558 |
|
| 1996 |
Evans PA, Roseman JD, Garber LT. An iterative approach to biologically important fused polycyclic ethers via acyl radical cyclizations Journal of Organic Chemistry. 61: 4880-4881. DOI: 10.1021/Jo9605861 |
0.322 |
|
| 1996 |
Magnus P, Lacour J, Evans PA, Roe MB, Hulme C. Hypervalent Iodine Chemistry: New Oxidation Reactions Using the Iodosylbenzene−Trimethylsilyl Azide Reagent Combination. Direct α- and β-Azido Functionalization of Triisopropylsilyl Enol Ethers Journal of the American Chemical Society. 118: 3406-3418. DOI: 10.1021/Ja953906R |
0.616 |
|
| 1996 |
Evans PA, Brandt TA. Enantioselective allylic substitution using a novel (phosphino-1,3-oxazine)palladium catalyst Tetrahedron Letters. 37: 9143-9146. DOI: 10.1016/S0040-4039(96)02162-4 |
0.374 |
|
| 1996 |
Evans PA, Brandt TA. Novel haloacetoxylation of 1,4-dimethoxynaphthalenes using hypervalent iodine chemistry Tetrahedron Letters. 37: 6443-6446. DOI: 10.1016/0040-4039(96)01427-X |
0.313 |
|
| 1996 |
Evans PA, Garber LT. Diastereoselective formation of cyclic acetals via an intramolecular fluoride-catalyzed hetero-Michael reaction Tetrahedron Letters. 37: 2927-2930. DOI: 10.1016/0040-4039(96)00449-2 |
0.34 |
|
| 1996 |
Evans PA, Brandt TA. Palladium catalyzed cross-coupling acylation approach to the antitumor antibiotic Fredericamycin A Tetrahedron Letters. 37: 1367-1370. DOI: 10.1016/0040-4039(96)00055-X |
0.36 |
|
| 1995 |
Evans PA, Holmes AB, Collins I, Raithby PR, Russell K. The first example of a transoid amide (imide) in an eight-membered lactam Journal of the Chemical Society, Chemical Communications. 2325-2326. DOI: 10.1039/C39950002325 |
0.505 |
|
| 1995 |
Evans PA, Nelson JD, Stanley AL. Directed Lithiation/Transmetalation Approach to Palladium-Catalyzed Cross-Coupling Acylation Reactions Journal of Organic Chemistry. 60: 2298-2301. DOI: 10.1021/Jo00112A067 |
0.364 |
|
| 1995 |
Evans PA, Longmire JM, Modi DP. Regioselective preparation of α,β-unsaturated ketones via the direct dehydrogenation of triisopropylsilyl enol ethers Tetrahedron Letters. 36: 3985-3988. DOI: 10.1016/0040-4039(95)00694-8 |
0.307 |
|
| 1995 |
Evans PA, Roseman JD. Stereoselective synthesis of cis-2,5-disubstituted tetrahydrofuran-3-ones via an acyl radical cyclization Tetrahedron Letters. 36: 31-34. DOI: 10.1016/0040-4039(94)02162-5 |
0.383 |
|
| 1994 |
Evans PA, Holmes AB, Russell K. New synthetic methodology for the synthesis of 7-substituted tetrahydroazepin-2-ones Journal of the Chemical Society-Perkin Transactions 1. 3397-3409. DOI: 10.1039/P19940003397 |
0.555 |
|
| 1994 |
Evans PA, Longmire JM. Regioselective preparation of α-nitro cyclohexyl triisopropylsilyl enol ethers Tetrahedron Letters. 35: 8345-8348. DOI: 10.1016/S0040-4039(00)74403-0 |
0.334 |
|
| 1990 |
Evans PA, Holmes AB, Russell K. Synthesis of homochiral unsaturated seven-membered lactams Tetrahedron-Asymmetry. 1: 593-596. DOI: 10.1016/0957-4166(90)80009-N |
0.581 |
|
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