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Daniele Rocco,
Ana A. Folgueiras-Amador,
Richard C. D. Brown and
Marta Feroci

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Beilstein J. Org. Chem. 2022, 18, 979–990, doi:10.3762/bjoc.18.98

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Marion Ringel,
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Bernhard Loll,
Thomas Brück and
Dan T. Major

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Naruhiro Yoshida,
Toru Amaya and
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Full Research Paper
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Beilstein J. Org. Chem. 2022, 18, 963–971, doi:10.3762/bjoc.18.96

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Electroreductive coupling of 2-acylbenzoates with α,β-unsaturated carbonyl compounds: density functional theory study on product selectivity

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Full Research Paper
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Beilstein J. Org. Chem. 2022, 18, 956–962, doi:10.3762/bjoc.18.95

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Valentin H. K. Fell,
Joseph Cameron,
Alexander L. Kanibolotsky,
Eman J. Hussien and
Peter J. Skabara

Full Research Paper
Published 01 Aug 2022

Beilstein J. Org. Chem. 2022, 18, 944–955, doi:10.3762/bjoc.18.94

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On Reuben G. Jones synthesis of 2-hydroxypyrazines

Pierre Legrand and
Yves L. Janin

Full Research Paper
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Beilstein J. Org. Chem. 2022, 18, 935–943, doi:10.3762/bjoc.18.93

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Morita–Baylis–Hillman reaction of 3-formyl-9H-pyrido[3,4-b]indoles and fluorescence studies of the products

Nisha Devi and
Virender Singh

Full Research Paper
Published 26 Jul 2022

Beilstein J. Org. Chem. 2022, 18, 926–934, doi:10.3762/bjoc.18.92

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Anti-inflammatory aromadendrane- and cadinane-type sesquiterpenoids from the South China Sea sponge Acanthella cavernosa

Shou-Mao Shen,
Qing Yang,
Yi Zang,
Jia Li,
Xueting Liu and
Yue-Wei Guo

Full Research Paper
Published 25 Jul 2022

Beilstein J. Org. Chem. 2022, 18, 916–925, doi:10.3762/bjoc.18.91

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Synthetic strategies for the preparation of γ-phostams: 1,2-azaphospholidine 2-oxides and 1,2-azaphospholine 2-oxides

Jiaxi Xu

Review
Published 22 Jul 2022

Beilstein J. Org. Chem. 2022, 18, 889–915, doi:10.3762/bjoc.18.90

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Efficient production of clerodane and ent-kaurane diterpenes through truncated artificial pathways in Escherichia coli

Fang-Ru Li,
Xiaoxu Lin,
Qian Yang,
Ning-Hua Tan and
Liao-Bin Dong

Full Research Paper
Published 21 Jul 2022

Beilstein J. Org. Chem. 2022, 18, 881–888, doi:10.3762/bjoc.18.89

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Supporting Information File 1: Experimental procedures, characterization data, and copies of ¹H and ¹³C NMR spectra are available.
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Enantioselective dioxytosylation of styrenes using lactate-based chiral hypervalent iodine(III)

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Hypervalent iodine chemistry in organic synthesis

Latest Articles

First example of organocatalysis by cathodic N-heterocyclic carbene generation and accumulation using a divided electrochemical flow cell

Understanding the competing pathways leading to hydropyrene and isoelisabethatriene

Electrochemical and spectroscopic properties of twisted dibenzo[g,p]chrysene derivatives

Electroreductive coupling of 2-acylbenzoates with α,β-unsaturated carbonyl compounds: density functional theory study on product selectivity

Introducing a new 7-ring fused diindenone-dithieno[3,2-b:2',3'-d]thiophene unit as a promising component for organic semiconductor materials

On Reuben G. Jones synthesis of 2-hydroxypyrazines

Morita–Baylis–Hillman reaction of 3-formyl-9H-pyrido[3,4-b]indoles and fluorescence studies of the products

Anti-inflammatory aromadendrane- and cadinane-type sesquiterpenoids from the South China Sea sponge Acanthella cavernosa

Synthetic strategies for the preparation of γ-phostams: 1,2-azaphospholidine 2-oxides and 1,2-azaphospholine 2-oxides

Efficient production of clerodane and ent-kaurane diterpenes through truncated artificial pathways in Escherichia coli

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