Brendan Parr
Affiliations: | 2014- | Chemistry | Yale University, New Haven, CT |
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"Brendan Parr"Mean distance: 8.26 | S | N | B | C | P |
Parents
Sign in to add mentorHuw M. L. Davies | grad student | 2013 | Emory |
Seth B. Herzon | post-doc | 2014- | Yale |
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Publications
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Bettencourt CJ, Krainz T, Chow S, et al. (2022) Unearthing the Subtleties of Rhodium(II)-Catalyzed Carbenoid Cycloadditions to Furans with an -Sulfonyl-1,2,3-triazole Probe. Organic Letters |
Labadie SS, Thai K, Grandner JM, et al. (2021) Enyne Amides to Fused Pyridones: Scope and Limitations. The Journal of Organic Chemistry |
Economou C, Romaire JP, Scott TZ, et al. (2018) A convergent approach to batzelladine alkaloids. Total syntheses of (+)-batzelladine E, (-)-dehydrobatzelladine C, and (+)-batzelladine K. Tetrahedron. 74: 3188-3197 |
Economou C, Romaire JP, Scott TZ, et al. (2018) A convergent approach to batzelladine alkaloids. Total syntheses of (+)-batzelladine E, (−)-dehydrobatzelladine C, and (+)-batzelladine K Tetrahedron. 74: 3188-3197 |
Parr BT, Economou C, Herzon SB. (2015) A concise synthesis of (+)-batzelladine B from simple pyrrole-based starting materials. Nature. 525: 507-10 |
Parr BT, Davies HM. (2015) Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence. Organic Letters. 17: 794-7 |
Parr BT, Davies HML. (2015) Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence Organic Letters. 17: 794-797 |
Parr BT, Davies HM. (2014) Highly stereoselective synthesis of cyclopentanes bearing four stereocentres by a rhodium carbene-initiated domino sequence. Nature Communications. 5: 4455 |
Parr BT, Davies HML. (2014) Highly stereoselective synthesis of cyclopentanes bearing four stereocentres by a rhodium carbene-initiated domino sequence Nature Communications. 5 |
Parr BT, Davies HM. (2013) 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 |