Scale-Up Investigation of Aggarwal Enal Bicyclic Intermediate Synthesis von Pelšs, Andrejs, Shubin, Kirill

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Streamlined transformations of bicyclic enal intermediate – formal synthesis of Δ12-Prostaglandin J3 von Pelšs, Andrejs, Černobrovkins, Dmitrijs, Shubin, Kirill

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Highly Chemoselective Copper-Catalyzed Conjugate Reduction of Stereochemically Labile α,β-Unsaturated Amino Ketones von Pelšs, Andrejs, Kumpulainen, Esa T. T, Koskinen, Ari M. P

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Reoptimization of the Organocatalyzed Double Aldol Domino Process to a Key Enal Intermediate and Its Application to the Total Synthesis of Δ12‐Prostaglandin J3 von Pelšs, Andrejs, Gandhamsetty, Narasimhulu, Smith, James R., Mailhol, Damien, Silvi, Mattia, Watson, Andrew J. A., Perez‐Powell, Isabel, Prévost, Sébastien, Schützenmeister, Nina, Moore, Peter R., Aggarwal, Varinder K.

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Reoptimization of the Organocatalyzed Double Aldol Domino Process to a Key Enal Intermediate and Its Application to the Total Synthesis of Δ 12 -Prostaglandin J 3 von Pelšs, Andrejs, Gandhamsetty, Narasimhulu, Smith, James R, Mailhol, Damien, Silvi, Mattia, Watson, Andrew J A, Perez-Powell, Isabel, Prévost, Sébastien, Schützenmeister, Nina, Moore, Peter R, Aggarwal, Varinder K

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Crystal structure of 3-amino-5,5-dimethyl-2-[( E )-2-nitroethenyl]cyclohex-2-en-1-one von Vigante, Brigita, Stepanovs, Dmitrijs, Pelss, Andrejs, Mishnev, Anatoly

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Crystal structure of 3-amino-5,5-dimethyl-2-[(E)-2-nitro-ethen-yl]cyclo-hex-2-en-1-one von Vigante, Brigita, Stepanovs, Dmitrijs, Pelss, Andrejs, Mishnev, Anatoly

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ChemInform Abstract: Highly Chemoselective Copper-Catalyzed Conjugate Reduction of Stereochemically Labile α,β-Unsaturated Amino Ketones von Pelss, Andrejs, Kumpulainen, Esa T. T., Koskinen, Ari M. P.

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