A proposed sustainability index for synthesis plans based on input provenance and output fate: application to academic and industrial synthesis plans for vanillin as a case study

John Andraos

Full Research Paper
Published 25 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2346–2362, doi:10.3762/bjoc.16.196

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David Van Craen,
Jenny Begall,
Johannes Großkurth,
Leonard Himmel,
Oliver Linnenberg,
Elisabeth Isaak and
Markus Albrecht

Full Research Paper
Published 24 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2338–2345, doi:10.3762/bjoc.16.195

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Host–guest interaction of cucurbit[8]uril with oroxin A and its effect on the properties of oroxin A

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Jun Xie,
Guangyan Luo,
Zhu Tao and
Qianjun Zhang

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Beilstein J. Org. Chem. 2020, 16, 2332–2337, doi:10.3762/bjoc.16.194

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Synthesis of 1,4-benzothiazinones from acylpyruvic acids or furan-2,3-diones and o-aminothiophenol

Ekaterina E. Stepanova,
Maksim V. Dmitriev and
Andrey N. Maslivets

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Published 21 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2322–2331, doi:10.3762/bjoc.16.193

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Design and synthesis of a bis-macrocyclic host and guests as building blocks for small molecular knots

Elizabeth A. Margolis,
Rebecca J. Keyes,
Stephen D. Lockey IV and
Edward E. Fenlon

Full Research Paper
Published 18 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2314–2321, doi:10.3762/bjoc.16.192

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Chan–Evans–Lam N1-(het)arylation and N1-alkеnylation of 4-fluoroalkylpyrimidin-2(1H)-ones

Viktor M. Tkachuk,
Oleh O. Lukianov,
Mykhailo V. Vovk,
Isabelle Gillaizeau and
Volodymyr A. Sukach

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Published 17 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2304–2313, doi:10.3762/bjoc.16.191

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Formation of an exceptionally stable ketene during phototransformations of bicyclo[2.2.2]oct-5-en-2-ones having mixed chromophores

Asitanga Ghosh

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Published 15 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2297–2303, doi:10.3762/bjoc.16.190

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Styryl-based new organic chromophores bearing free amino and azomethine groups: synthesis, photophysical, NLO, and thermal properties

Anka Utama Putra,
Deniz Çakmaz,
Nurgül Seferoğlu,
Alberto Barsella and
Zeynel Seferoğlu

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Published 14 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2282–2296, doi:10.3762/bjoc.16.189

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The B & B approach: Ball-milling conjugation of dextran with phenylboronic acid (PBA)-functionalized BODIPY

Patrizia Andreozzi,
Lorenza Tamberi,
Elisamaria Tasca,
Gina Elena Giacomazzo,
Marta Martinez,
Mirko Severi,
Marco Marradi,
Stefano Cicchi,
Sergio Moya,
Giacomo Biagiotti and
Barbara Richichi

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Published 11 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2272–2281, doi:10.3762/bjoc.16.188

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Tools for generating and analyzing glycan microarray data

Akul Y. Mehta,
Jamie Heimburg-Molinaro and
Richard D. Cummings

Review
Published 10 Sep 2020

Beilstein J. Org. Chem. 2020, 16, 2260–2271, doi:10.3762/bjoc.16.187

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Supporting Information File 1: Spectrophotometric characterisation in solution, NMR and HRMS data, additional experimental data on interactions with DNA/RNA.
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Naphthalene diimide bis-guanidinio-carbonyl-pyrrole as a pH-switchable threading DNA intercalator

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Latest Articles

A proposed sustainability index for synthesis plans based on input provenance and output fate: application to academic and industrial synthesis plans for vanillin as a case study

Hierarchically assembled helicates as reaction platform – from stoichiometric Diels–Alder reactions to enamine catalysis

Host–guest interaction of cucurbit[8]uril with oroxin A and its effect on the properties of oroxin A

Synthesis of 1,4-benzothiazinones from acylpyruvic acids or furan-2,3-diones and o-aminothiophenol

Design and synthesis of a bis-macrocyclic host and guests as building blocks for small molecular knots

Chan–Evans–Lam N1-(het)arylation and N1-alkеnylation of 4-fluoroalkylpyrimidin-2(1H)-ones

Formation of an exceptionally stable ketene during phototransformations of bicyclo[2.2.2]oct-5-en-2-ones having mixed chromophores

Styryl-based new organic chromophores bearing free amino and azomethine groups: synthesis, photophysical, NLO, and thermal properties

The B & B approach: Ball-milling conjugation of dextran with phenylboronic acid (PBA)-functionalized BODIPY

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