Chemistry in flow systems II

• Andreas Kirschning

Beilstein J. Org. Chem. 2011, 7, 1046–1047, doi:10.3762/bjoc.7.119

• the scope of this enabling technology with far reaching implications even for industrial biotechnology. I am thankful to all my colleagues who have helped to create this diverse and state of the art flow series. Finally, special thanks are dedicated to the staff of the Beilstein-Institut for their

Synthesis of glycoconjugate fragments of mycobacterial phosphatidylinositol mannosides and lipomannan

• Benjamin Cao,
• Jonathan M. White and
• Spencer J. Williams

Beilstein J. Org. Chem. 2011, 7, 369–377, doi:10.3762/bjoc.7.47

• Benjamin Cao Jonathan M. White Spencer J. Williams School of Chemistry and Bio21 Molecular Science and Biotechnology Institute, University of Melbourne, Parkville, Victoria, Australia, Fax: +61 3 9347 8124; Tel: +61 3 8344 2422 10.3762/bjoc.7.47 Abstract Mycobacterium tuberculosis, the causitive

Michael-type addition of azoles of broad-scale acidity to methyl acrylate

• Sławomir Boncel,
• Kinga Saletra,
• Barbara Hefczyc and
• Krzysztof Z. Walczak

Beilstein J. Org. Chem. 2011, 7, 173–178, doi:10.3762/bjoc.7.24

• Slawomir Boncel Kinga Saletra Barbara Hefczyc Krzysztof Z. Walczak Silesian University of Technology, Department of Organic Chemistry, Bioorganic Chemistry and Biotechnology, Krzywoustego 4, 44-100 Gliwice, Poland, Tel.: +48 32 237 1792, Fax: +48 32 237 2094 Silesian University of Technology

SbCl₃-catalyzed one-pot synthesis of 4,4′-diaminotriarylmethanes under solvent-free conditions: Synthesis, characterization, and DFT studies

• Ghasem Rezanejade Bardajee

Beilstein J. Org. Chem. 2011, 7, 135–144, doi:10.3762/bjoc.7.19

• [11][12][13], antitubercular [14], anti-infective, and antimicrobial activity [15]. Additionally, they have been used for sterilization of trypanosome cruizi-infected blood [16], in biotechnology process control [17][18], in dye-assisted laser inactivation of enzymes [19], in wastewater treatment

The C–F bond as a conformational tool in organic and biological chemistry

• Luke Hunter

Beilstein J. Org. Chem. 2010, 6, No. 38, doi:10.3762/bjoc.6.38

• ]. The concept of controlling peptide conformation using fluorine atoms is exciting because the conformation of a peptide critically affects its biological activity and consequently, there are many potential applications in medicinal chemistry and biotechnology. Collagen Collagen is the most abundant

• properties of functional molecules to be optimised through selective fluorination chemistry. This concept has been demonstrated in diverse areas including medicine, catalysis, materials science and biotechnology. It is hoped that the examples highlighted in this review have persuaded the reader of the great

Synthesis of gem-difluoromethylenated analogues of boronolide

• Jing Lin,
• Xiao-Long Qiu and
• Feng-Ling Qing

Beilstein J. Org. Chem. 2010, 6, No. 37, doi:10.3762/bjoc.6.37

• Jing Lin Xiao-Long Qiu Feng-Ling Qing College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, 2999 North Renmin Lu, Shanghai 201620, China Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu

Symmetrical and unsymmetrical α,ω-nucleobase amide-conjugated systems

• Sławomir Boncel,
• Maciej Mączka,
• Krzysztof K. K. Koziol,
• Radosław Motyka and
• Krzysztof Z. Walczak

Beilstein J. Org. Chem. 2010, 6, No. 34, doi:10.3762/bjoc.6.34

• Slawomir Boncel Maciej Maczka Krzysztof K. K. Koziol Radoslaw Motyka Krzysztof Z. Walczak Silesian University of Technology, Department of Organic Chemistry, Biochemistry and Biotechnology, Krzywoustego 4, 44-100 Gliwice, Poland, Tel.: +48 32 237 1792, Fax: +48 32 237 2094 University of Cambridge

Understanding the mechanism of Pd-catalyzed allylic substitution of the cyclic difluorinated carbonates

• Jun Xu,
• Xiao-Long Qiu and
• Feng-Ling Qing

Beilstein J. Org. Chem. 2008, 4, No. 18, doi:10.3762/bjoc.4.18

• Jun Xu Xiao-Long Qiu Feng-Ling Qing Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, 2999 North Renmin Lu

Synthesis of the Benzo- fused Indolizidine Alkaloid Mimics

• Daniel L. Comins and
• Kazuhiro Higuchi

Beilstein J. Org. Chem. 2007, 3, No. 42, doi:10.1186/1860-5397-3-42

• by grants from the North Carolina Biotechnology Center and the National Science Foundation (Grant CHE-0078253).

N-1 regioselective Michael- type addition of 5-substituted uracils to (2-hydroxyethyl) acrylate

• Sławomir Boncel,
• Dominika Osyda and
• Krzysztof Z. Walczak

Beilstein J. Org. Chem. 2007, 3, No. 40, doi:10.1186/1860-5397-3-40

• Slawomir Boncel Dominika Osyda Krzysztof Z. Walczak Department of Organic Chemistry, Biochemistry and Biotechnology Silesian University of Technology, Krzywoustego 4, PL-44100 Gliwice, Poland 10.1186/1860-5397-3-40 Abstract N-1 regioselective Michael-type addition of 5-substituted uracils to (2