Independent
21. Hetero-Diels–Alder Reactions of (Isobenzo)Furans
C. J. DeAngelis, C. G. Newton*
submitted
20. Ketenimines as Aza-Dienophiles
C. J. DeAngelis,† G. Goyal,† M. J. Liss,† J. E. Budwitz, M. S. Herlihy, A. V. Conner, S. E. Wheeler, P. Ma, M. Li, K. N. Houk,* C. G. Newton*
J. Am. Chem. Soc. 2025, accepted
† Equal Contribution
• Preprint available on ChemRxiv, DOI: 10.26434/chemrxiv-2024-7rvht
19. Synthesis of a 2,5-Bis(tert-butyldimethylsilyloxy)furan and its Reaction with Benzyne
J. E. Budwitz, C. G. Newton*
Org. Synth. 2023, 100, 159
• Invited Submission
18. Early Career Author Profile
C. G. Newton*
Helv. Chim. Acta 2023, 106, e202300007
17. Ring Forming Approaches to para-Quinones: Toward a General Diels–Alder Disconnection
J. E. Budwitz, C. G. Newton*
Synlett 2022, 33, 1473
• Invited “Synpacts” Article
16. Bisketene Equivalents as Diels–Alder Dienes
I. Dissanayake,† J. D. Hart,† E. C. Becroft, C. J. Sumby, C. G. Newton*
J. Am. Chem. Soc. 2020, 142, 13328
† Equal Contribution
• Preprint available on ChemRxiv, DOI: 10.26434/chemrxiv.12463949
• Highlighted in: ChemViews Mag. 2020, DOI: 10.1002/chemv.202000072
• Highlighted in: Chemistry in Australia, September–November 2020, 12
15. Network Analysis of Substituted Bullvalenes
O. Yahiaoui, L. F. Pašteka,* C. J. Blake, C. G. Newton, T. Fallon
Org. Lett. 2019, 21, 9574
14. Visible Light Photoredox Catalysis Enables the Biomimetic Synthesis of Nyingchinoids A, B and D, and Rasumatranin D
J. D. Hart, L. Burchill, A. J. Day, C. G. Newton, C. J. Sumby, D. M. Huang, J. H. George*
Angew. Chem. Int. Ed. 2019, 58, 2791
Mentored
13. A Broad-Spectrum Synthesis of Tetravinylethylenes
K. L. Horvath, C. G. Newton, K. A. Roper, J. S. Ward, M. S. Sherburn
Chem. Eur. J. 2019, 25, 4072
12. Chiral Cp Ligands for Rhodium(III)-Catalyzed Asymmetric Carbon−Hydrogen Bond Functionalization
C. G. Newton, N. Cramer
in Rhodium Catalysis in Organic Synthesis: Methods and Reactions (eds. K. Tanaka), Wiley-VCH, Weinheim, 2019
11. Axially Chiral Dibenzazepinones by a Palladium(0)‐Catalyzed Atropo‐enantioselective C−H Arylation
C. G. Newton, E. Braconi,† J. Kuziola,† M. D. Wodrich, N. Cramer*
Angew. Chem. Int. Ed. 2018, 57, 11040 († Equal Contribution)
10. One‐Step Multigram‐Scale Biomimetic Synthesis of Psiguadial B
C. G. Newton, D. N. Tran, M. D. Wodrich, N. Cramer*
Angew. Chem. Int. Ed. 2017, 56, 13776
9. Catalytic Enantioselective Transformations Involving C−H Bond Cleavage by Transition-Metal Complexes
C. G. Newton,† S.-G. Wang,† C. C. Oliveira, N. Cramer*
Chem. Rev. 2017, 117, 8908
† Equal Contribution
8. Masked Ketenes as Dienophiles in the Diels–Alder Reaction
E. G. Mackay,* C. G. Newton*
Aus. J. Chem. 2016, 69, 1365
7. Cross-Conjugation in Synthesis
C. G. Newton, M. S. Sherburn*
in Cross Conjugation: Modern Dendralene, Radialene and Fulvene Chemistry (eds. H. Hopf, M. S. Sherburn), Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2016
6. Asymmetric Catalysis Powered by Chiral Cyclopentadienyl Ligands
C. G. Newton, D. Kossler, N. Cramer*
J. Am. Chem. Soc. 2016, 138, 3935
5. [5]Radialene
E. G. Mackay, C. G. Newton, H. Toombs-Ruane, E. J. Lindeboom, T. Fallon, A. C. Willis, M. N. Paddon-Row,* M. S. Sherburn*
J. Am. Chem. Soc. 2015, 137, 14653
4. Total Synthesis of the Pseudopterosin Aglycones
C. G. Newton, M. S. Sherburn*
Nat. Prod. Rep. 2015, 32, 865
3. Pseudopterosin Synthesis From a Chiral Cross-Conjugated Hydrocarbon Through a Series of Cycloadditions
C. G. Newton, S. L. Drew, A. L. Lawrence, A. C. Willis, M. N. Paddon-Row,* M. S. Sherburn*
Nat. Chem. 2015, 7, 82
2. 1,1-Divinylallene
K. M. Cergol, C. G. Newton, A. L. Lawrence, A. C. Willis, M. N. Paddon-Row,* M. S. Sherburn*
Angew. Chem. Int. Ed. 2011, 50, 10425
1. The Anti-Cancer, Anti-Inflammatory and Tuberculostatic Activities of a Series of 6,7-Substituted-5,8-Quinolinequinones
B. J. Mulchin, C. G. Newton, J. W. Baty, C. H. Grasso, W. John Martin, M. C. Walton, E. M. Dangerfield, C. H. Plunkett, M. V. Berridge, J. L. Harper, M. S. M. Timmer,* B. L. Stocker*
Bioorg. Med. Chem. 2010, 18, 3238