| Year |
Citation |
Score |
| 2022 |
Bettencourt CJ, Krainz T, Chow S, Parr BT, Tracy WF, Bernhardt PV, Davies HML, Williams CM. Unearthing the Subtleties of Rhodium(II)-Catalyzed Carbenoid Cycloadditions to Furans with an -Sulfonyl-1,2,3-triazole Probe. Organic Letters. PMID 36512372 DOI: 10.1021/acs.orglett.2c03869 |
0.652 |
|
| 2021 |
Labadie SS, Thai K, Grandner JM, Liu Y, Parr BT. Enyne Amides to Fused Pyridones: Scope and Limitations. The Journal of Organic Chemistry. PMID 34337936 DOI: 10.1021/acs.joc.1c00688 |
0.395 |
|
| 2018 |
Economou C, Romaire JP, Scott TZ, Parr BT, Herzon SB. A convergent approach to batzelladine alkaloids. Total syntheses of (+)-batzelladine E, (-)-dehydrobatzelladine C, and (+)-batzelladine K. Tetrahedron. 74: 3188-3197. PMID 33911315 DOI: 10.1016/j.tet.2018.04.050 |
0.584 |
|
| 2018 |
Economou C, Romaire JP, Scott TZ, Parr BT, Herzon SB. A convergent approach to batzelladine alkaloids. Total syntheses of (+)-batzelladine E, (−)-dehydrobatzelladine C, and (+)-batzelladine K Tetrahedron. 74: 3188-3197. DOI: 10.1016/J.Tet.2018.04.050 |
0.575 |
|
| 2015 |
Parr BT, Economou C, Herzon SB. A concise synthesis of (+)-batzelladine B from simple pyrrole-based starting materials. Nature. 525: 507-10. PMID 26375010 DOI: 10.1038/Nature14902 |
0.589 |
|
| 2015 |
Parr BT, Davies HM. Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence. Organic Letters. 17: 794-7. PMID 25665081 DOI: 10.1021/Ol503508K |
0.629 |
|
| 2015 |
Parr BT, Davies HML. Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence Organic Letters. 17: 794-797. DOI: 10.1021/ol503508k |
0.377 |
|
| 2014 |
Parr BT, Davies HM. Highly stereoselective synthesis of cyclopentanes bearing four stereocentres by a rhodium carbene-initiated domino sequence. Nature Communications. 5: 4455. PMID 25082301 DOI: 10.1038/Ncomms5455 |
0.623 |
|
| 2014 |
Parr BT, Davies HML. Highly stereoselective synthesis of cyclopentanes bearing four stereocentres by a rhodium carbene-initiated domino sequence Nature Communications. 5. DOI: 10.1038/ncomms5455 |
0.349 |
|
| 2013 |
Parr BT, Davies HM. Rhodium-catalyzed tandem cyclopropanation/Cope rearrangement of 4-alkenyl-1-sulfonyl-1,2,3-triazoles with dienes. Angewandte Chemie (International Ed. in English). 52: 10044-7. PMID 23913819 DOI: 10.1002/Anie.201304310 |
0.61 |
|
| 2013 |
Parr BT, Green SA, Davies HM. Rhodium-catalyzed conversion of furans to highly functionalized pyrroles. Journal of the American Chemical Society. 135: 4716-8. PMID 23477809 DOI: 10.1021/Ja401386Z |
0.596 |
|
| 2013 |
Parr BT, Davies HML. Rhodium-catalyzed tandem cyclopropanation/cope rearrangement of 4-alkenyl-1-sulfonyl-1,2,3-triazoles with dienes Angewandte Chemie - International Edition. 52: 10044-10047. DOI: 10.1002/anie.201304310 |
0.423 |
|
| 2012 |
Li Z, Parr BT, Davies HM. Highly stereoselective C-C bond formation by rhodium-catalyzed tandem ylide formation/[2,3]-sigmatropic rearrangement between donor/acceptor carbenoids and chiral allylic alcohols. Journal of the American Chemical Society. 134: 10942-6. PMID 22694052 DOI: 10.1021/Ja303023N |
0.575 |
|
| 2011 |
Parr BT, Li Z, Davies HM. Asymmetric Synthesis of Highly Functionalized Cyclopentanes by a Rhodium- and Scandium-Catalyzed Five-Step Domino Sequence. Chemical Science (Royal Society of Chemistry : 2010). 2: 2378-2382. PMID 22708053 DOI: 10.1039/C1Sc00434D |
0.643 |
|
| 2011 |
Hansen JH, Parr BT, Pelphrey P, Jin Q, Autschbach J, Davies HM. Rhodium(II)-catalyzed cross-coupling of diazo compounds. Angewandte Chemie (International Ed. in English). 50: 2544-8. PMID 21370334 DOI: 10.1002/Anie.201004923 |
0.612 |
|
| 2011 |
Parr BT, Li Z, Davies HML. Asymmetric synthesis of highly functionalized cyclopentanes by a rhodium- and scandium-catalyzed five-step domino sequence Chemical Science. 2: 2378-2382. DOI: 10.1039/c1sc00434d |
0.549 |
|
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