scholarly journals Front Cover Picture: Catalytic One-Pot Oxetane to Carbamate Conversions: Formal Synthesis of Drug Relevant Molecules (Adv. Synth. Catal. 10/2016)

2016 ◽  
Vol 358 (10) ◽  
pp. 1547-1547
Author(s):  
Wusheng Guo ◽  
Victor Laserna ◽  
Jeroen Rintjema ◽  
Arjan W. Kleij
Keyword(s):  
One Pot ◽  
Formal Synthesis ◽  
Front Cover

scholarly journals Catalytic One-Pot Oxetane to Carbamate Conversions: Formal Synthesis of Drug Relevant Molecules

2016 ◽  
Vol 358 (10) ◽  
pp. 1602-1607 ◽  
Author(s):  
Wusheng Guo ◽  
Victor Laserna ◽  
Jeroen Rintjema ◽  
Arjan W. Kleij
Keyword(s):  
One Pot ◽  
Formal Synthesis

scholarly journals Front Cover: Symmetry Breaking Induced by Growth Kinetics: One‐Pot Synthesis of Janus Au−AgBr Nanoparticles (ChemNanoMat 10/2020)

ChemNanoMat ◽  
2020 ◽  
Vol 6 (10) ◽  
pp. 1417-1417
Author(s):  
Reki Takahashi ◽  
Musashi Fujishima ◽  
Hiroaki Tada ◽  
Tetsuro Soejima
Keyword(s):  
Symmetry Breaking ◽  
Growth Kinetics ◽  
One Pot ◽  
Front Cover ◽  
One Pot Synthesis

scholarly journals Front Cover Picture: Synthesis of Substituted 4‐Arylamino‐1,2‐naphthoquinones in One‐Pot Reactions Using CotA‐Laccase as Biocatalyst (Adv. Synth. Catal. 16/2020)

2020 ◽  
Vol 362 (16) ◽  
pp. 3257-3257
Author(s):  
Ana Catarina Sousa ◽  
Iolanda Santos ◽  
M. F. M. M. Piedade ◽  
Lígia O. Martins ◽  
M. Paula Robalo
Keyword(s):  
One Pot ◽  
Front Cover ◽  
Cota Laccase

scholarly journals One-pot formal synthesis of biorenewable terephthalic acid from methyl coumalate and methyl pyruvate

2014 ◽  
Vol 16 (4) ◽  
pp. 2111-2116 ◽  
Author(s):  
Jennifer J. Lee ◽  
George A. Kraus
Keyword(s):  
Aromatic Compounds ◽  
Terephthalic Acid ◽  
One Pot ◽  
Formal Synthesis ◽  
Methyl Pyruvate

Diverse functionalized aromatic compounds including DMT are constructed from captodative dienophiles with exclusive regioselectivity.

Formal Synthesis of Actinoranone Using a Racemization-Free One-Pot Semipinacol Rearrangement/Wittig Reaction

2018 ◽  
Author(s):  
Martina Menger ◽  
Mathias Christmann
Keyword(s):  
Natural Product ◽  
Wittig Reaction ◽  
Reaction Sequence ◽  
One Pot ◽  
Formal Synthesis ◽  
Linear Sequence ◽  
Semipinacol Rearrangement ◽  
Key Steps

Here, we report a formal synthesis of the marine cytotoxic meroterpenoid actinoranone. Key steps include a racemization-free semipinacol rearrangement/Wittig reaction sequence and a chiral pool approach for the syntheses of the tetralone and the decalin fragments, respectively. The presented route provides access to the natural product in 14 steps in the longest linear sequence.

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