Thomas R.R. Pettus, Ph.D.
Affiliations: | Chemistry and Biochemistry | University of California, Santa Barbara, Santa Barbara, CA, United States |
Area:
synthetic organic chemistry, o-quinone methides, cyclohexadienones,Website:
http://www.chem.ucsb.edu/people/tom-r-pettusGoogle:
"Thomas Pettus"Mean distance: 7.3 | S | N | B | C | P |
Parents
Sign in to add mentorTomas Hudlicky | research assistant | 1987-1989 | Virginia Tech | |
Richard H. Schlessinger | grad student | 1990-1996 | Rochester | |
(Chiral Amino Furans) | ||||
Samuel J. Danishefsky | post-doc | 1996-1998 | Columbia |
Children
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Publications
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Pettus TR. (2023) Nucleophilic Addition of 4,5-Dihydrooxazole Derivatives to Base Generated o-Quinone Methides: A Four-Component Reaction The Journal of Organic Chemistry. 88: 2583-2588 |
Pettus TR. (2019) Nucleophilic Imines and Electrophilic o-Quinone Methides, a Three-Component Assembly of Assorted 3,4-Dihydro-2H-1,3-benzoxazines Organic Letters |
Pettus T, Feng Z, Burnett G. (2018) A Biomimetic Synthesis of des-Hydroxy Paecilospirone Synlett. 29: 1517-1519 |
Pettus T, Feng Z, Burnett G. (2018) A Biomimetic Synthesis of des-Hydroxy Paecilospirone Synlett. 29: 1517-1519 |
Pettus T, Feng Z, Burnett G. (2018) A Biomimetic Synthesis of des-Hydroxy Paecilospirone Synlett. 29: 1517-1519 |
Pettus T, Feng Z, Burnett G. (2018) A Biomimetic Synthesis of des-Hydroxy Paecilospirone Synlett. 29: 1517-1519 |
Feng ZG, Bai WJ, Pettus TR. (2015) Unified total syntheses of (-)-medicarpin, (-)-sophoracarpan A, and (±)-kushecarpin A with some structural revisions. Angewandte Chemie (International Ed. in English). 54: 1864-7 |
Bai WJ, David JG, Feng ZG, et al. (2014) The domestication of ortho-quinone methides. Accounts of Chemical Research. 47: 3655-64 |
David JG, Bai WJ, Weaver MG, et al. (2014) A general diastereoselective catalytic vinylogous aldol reaction among tetramic acid-derived pyrroles. Organic Letters. 16: 4384-7 |
Weaver MG, Bai WJ, Jackson SK, et al. (2014) Diels-Alder construction of regiodifferentiated meta-amino phenols and derivatives. Organic Letters. 16: 1294-7 |