Diversity-Oriented Synthesis of Nanographenes Enabled by Dearomative Annulative π-Extension

W. Matsuoka, H. Ita, D. Sarlah, K. Itami

Nature Commun., 2021, 12, 3940

Encyclopedia of Reagents for Organic Synthesis: 4-Methyl-1,2,4-triazoline-3,5-dione (MTAD)

M. Okumura, D. Sarlah

e-EROS. 2021, 1-11

Total Synthesis and Computational Investigations of Sesquiterpene-Tropolones Ameliorate Stereochemical Inconsistencies and Resolve an Ambiguous Biosynthetic Relationship

C. Y. Bemis, C. N. Ungarean, A. S. Shved, C. S. Jamieson, T. Hwang, K. S. Lee, K. N. Houk, and D. Sarlah

J. Am. Chem. Soc. 2021, 143, 15, 6006–6017

Total Synthesis of Stelletins through an Unconventional Annulation Strategy

C. J. Huck, Y. D. Boyko, D. Sarlah

Acc. Chem. Res. 2021, 54, 7, 1597–1609

Synthetic Studies on Selective, Proapoptotic Isomalabaricane Triterpenoids Aided by Computational Techniques

Y. Boyko, C. J. Huck, S. Ning, A. S. Shved, C. Yang, T. Chu, E. J. Tonogai, P. J. Hergenrother, D. Sarlah

J. Am. Chem. Soc. 2021, 143, 4, 2138–2155

Development of a Scalable and Sublimation-Free Route to MTAD

Z. Siddiqi, C. N. Ungarean, T. W. Bingham, D. Sarlah

Org. Process Res. Dev. 2020, 24, 12, 2953–2959

Structure Prediction and Synthesis of Pyridine-Based Macrocyclic Peptide Natural Products

G. A. Hudson, A. R. Hooper, A. J. DiCaprio, D. Sarlah, D. A. Mitchell

Org. Lett. 2021, 23, 2, 253–256

Arenophile-Mediated Photochemical Dearomatization of Nonactivated Arenes

M. Okumura, D. Sarlah

CHIMIA 2020, 74, 577-583

Shaping Molecular Landscapes: Recent Advances, Opportunities, and Challenges in Dearomatization

C. J. Huck, D. Sarlah

Chem 2020, 6, 1589-1603

A New Approach Towards The Synthesis of Bielschowskysin: Synthesis and Photochemistry of An Advanced Macrocyclic Enedione Intermediate

M. Nesic, M. M. Kincanon, D. B. Ryffel, D. Sarlah

Tetrahedron, 2020, 131318

Chemical Equivalent of Arene Monooxygenases: Dearomative Synthesis of Arene Oxides and Oxepines

Z. Siddiqi, W. C. Wertjes, D. Sarlah

J. Am. Chem. Soc. 2020, 142, 10125–10131

Visible-Light-Induced Dearomatizations

M. Okumura, D. Sarlah

Eur. J. Org. Chem. 2020, 10, 1259-1273

Palladium‐Catalyzed Dearomative syn‐1,4‐Oxyamination

C. Tang, M. Okumura, H. Deng, D. Sarlah

Angew. Chem. Int. Ed. 2019, 58, 15762–15766

The Total Synthesis of Isomalabaricane Triterpenoids

Y. Boyko, C. J. Huck, D. Sarlah

J. Am. Chem. Soc. 2019, 141, 14131–14135

Empowering Synthesis of Complex Natural Products

L. W. Hernandez, D. Sarlah

Chem. Eur. J. 2019, 25, 13248–13270

Palladium‐Catalyzed Dearomative syn‐1,4‐Carboamination with Grignard Reagents

C. Tang, M. Okumura, Y. Zhu, A. Hooper, Y. Lee, D. Sarlah

Angew. Chem. Int. Ed. 2019, 58, 10245–10249

Synthesis of Idarubicinone via Global Functionalization of Tetracene

D. G. Dennis, M. Okumura, D. Sarlah

J. Am. Chem. Soc. 2019, 141, 10193–10198

Palladium-Catalyzed Dearomative syn-1,4-Diamination

W. C. Wertjes, M. Okumura, D. Sarlah

J. Am. Chem. Soc. 2019, 141, 163–167

Enantioselective Synthesis of Isocarbostyril Alkaloids and Analogs Using Catalytic Dearomative Functionalization of Benzene

T. W. Bingham, L. W. Hernandez, D. G. Olson, R. L. Svec, P. J. Hergenrother, D. Sarlah

J. Am. Chem. Soc. 2019, 141, 657–670

Recent advances in chemical dearomatization of nonactivated arenes

W. C. Wertjes, E. H. Southgate, D. Sarlah

Chem. Soc. Rev. 2018, 47, 7996–8017

Nickel-Catalyzed Dearomative trans-1,2-Carboamination

L. W. Hernandez, U. Klöckner, J. Pospech, L. Hauss, D. Sarlah

J. Am. Chem. Soc. 2018, 140, 4503–4507

Arenophile-Mediated Dearomative Functionalization Strategies

M. Okumura, D. Sarlah

Synlett 2018, 29, 845–855

Palladium-Catalyzed Dearomative syn-1,4-Carboamination

M. Okumura, A. S. Shved, D. Sarlah

J. Am. Chem. Soc. 2017, 139, 17787–17790

Synthesis of (+)-Pancratistatins via Catalytic Desymmetrization of Benzene

L. W. Hernandez, J. Pospech, U. Kloeckner, T. W. Bingham, D. Sarlah

J. Am. Chem. Soc. 2017, 139, 15656–15659

Total Synthesis of Lycoricidine and Narciclasine by Chemical Dearomatization of Bromobenzene /Review article/

E. H. Southgate, D. R. Holycross, D. Sarlah

Angew. Chem. Int. Ed. 2017, 56, 15049–15052