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2022 – 2024

113. Sα-Amino bicycloalkylation through organophotoredox catalysis

Jeremy Nugent, Adrián López-Francés, Alistair J. Sterling, Min Yi Tay, Nils Frank, James J. Mousseau, Fernanda Duarte and Edward A. Anderson


Chem. Sci., 2024, Advance Article

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112. Synthesis and Evaluation of (Bis)benzyltetrahydroisoquinoline Alkaloids as Antiparasitic Agents

Ana Sozanschi, Hannah Asiki, Maiara Amaral, Erica V. de Castro Levatti, Andre G. Tempone, Richard J. Wheeler, and Edward A. Anderson

JACS Au. 2024 Article ASAP

doi: 10.1021/jacsau.4c00007

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111. Synthesis of Heterocycle-Substituted Bicyclo[3.1.1]heptanes and Aza-bicyclo[3.1.1]heptanes via Photocatalytic Minisci Reaction

Rebecca I. Revie, Benjamin J. Whitaker, Bhaskar Paul, Russell C. Smith, and Edward A. Anderson*

Org. Lett. 2024


110. Taming non-classical carbocations to control small ring reactivity

McNamee R, Frank N, Christensen K, Duarte F, Anderson E.

Sci. Adv. 2024 10 eadj9695


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109. Stereoselective Alder-Ene Reactions of Bicyclo[1.1.0]butanes: Facile Synthesis of Cyclopropyl- and Aryl-Substituted Cyclobutenes

A. Dasgupta, S. Bhattacharjee, Z. Tong, A. Guin, R. E. McNamee, K. E. Christensen, A. T. Biju, and E. A. Anderson

J. Am. Chem. Soc. 2024, 146, 1, 1196–1203

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108. Bridge Cross-Coupling of Bicyclo[1.1.0]butanes

R E. McNamee, A. Dasgupta,  K. E. Christensen and E. A. Anderson

Org. Lett. 2024, 26, 1, 360–364

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107. Gold-Catalyzed Cyclization of Yndiamides with Isoxazoles via α-Imino Gold Fischer Carbenes

Z. Tong, P. Smith, H. Pickford, K. Christensen and E. A. Anderson

Chem. Eur. J. 2023  e202302821.


106. Sequencing palladium-catalyzed cycloisomerization cascades in a synthesis of the gelsemine core

Liang G, Anderson E.

Chem. Sci. 2023 14, 6970-6974


105. Synthetic Study toward Triterpenes from the Schisandraceae Family of Natural Products

Kravljanac P, Anderson E.

Molecules 202328(11), 4468


104. Biological Activity and Structure−Activity Relationship of Dehydrodieugenol B Analogues against Visceral Leishmaniasis

M. Amaral, H. Asiki, C. E. Sear, S. Singh, P. Pieper, M. M. Haugland, E. A. Anderson and A. G. Tempone

RSC Med. Chem. 2023, 14, 1344-1350



103. Conquering the Synthesis and Functionalization of Bicyclo[1.1.1]pentanes

Shire BR, Anderson EA.

JACS Au, 20233, 6, 1539–1553


102. Chemoselective carbene insertion into the N−H bonds of NH3·H2O

Liu Z, Yang Y, Song Q, Li L, Zanoni G, Liu S, Xiang M, Anderson EA, Bi X.

Nat Commun. 2022, 13(1):7649



99. Synthesis of meta-substituted arene bioisosteres from [3.1.1]propellane

N. Frank, J. Nugent, B. Shire, H. Pickford, P. Rabe, A. Sterling, T. Zarganes-Tzitzikas, T. Grimes, A.Thompson, R. Smith, C. Schofield, P. Brennan, F. Duarte, E. Anderson*

Nature 2022, 611, 721–726


100. Rapid and scalable halosulfonylation of strain-release reagents

H. Pickford, V. Ripenko, R. McNamee, S. Holovchuk, A. Thompson,

R. Smith, P. Mykhailiuk, E. Anderson*

Angew. Chem. Int. Ed. 2023, 62, e202213508; 

Angew. Chem. 2023135, e202213508



101. Rhodium-Catalyzed [2 + 2 + 2] Cyclotrimerizations of Yndiamides with Alkynes

P. J. Smith, Z. Tong, J. Ragus, P. Solon, K. W. Shimkin, E. Anderson*

Org. Lett. 2022, 24, 41, 7522–7526


98. Collective Synthesis of Illudalane Sesquiterpenes via Cascade Inverse Electron Demand (4 + 2) Cycloadditions of Thiophene S, S-Dioxides


K.H.K Park, N. Frank, F. Duarte, E.A. Anderson*

J. Am. Chem. Soc. 2022,144, 22, 10017–10024

doi: 10.1021/jacs.2c03304

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97. Carbodefluorination of fluoroalkyl ketones via a carbene-initiated rearrangement strategy


L. Li, X. Zhang, Y. Ning, X. Zhang, B. Liu, Z.g Zhang, P. Sivaguru, G. Zanoni, S. Li, E. A. Anderson, X. Bi

Nat Commun. 2022, 13, 4280

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95. Synthesis of the C50 diastereomers of the C33-C51 fragment of stambomycin D


Y. Wang, V. Chintalapudi, H.G. Gudmundsson, G.L. Challis, E.A. Anderson* 

Org. Chem. Front., 2022, 9, 445-449


96. Silver-catalyzed site-selective C(sp3)−H benzylation of ethers with N-triftosylhydrazones


Z. Liu, H. Wang, P. Sivaguru, S. P. Nolan, Q. Song, W. Yu, X. Jiang, E. A. Anderson, X. Bi

Nat Commun. 2022, 13, 1674

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