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- Asymmetric reduction of ketones with recombinant E. coli whole cells in neat substrates. Andre Jakoblinnert, Radoslav Mladenov, Albert Paul, Fabrizio Sibilla, Ulrich Schwaneberg, Marion B. Ansorge-Schumacher, Pablo Domínguez de María
, Chem. Commun.
, 2011
, 47
, 12230
- The synthesis of non-racemic β-alkyl-β-aryl-disubstituted allyl alcohols and their transformation into allylamines and amino acids bearing a quaternary stereocenter. Aleksandra Narczyk, Michał Pieczykolan, Sebastian Stecko
, Org. Biomol. Chem.
, 2018
, 16
, 3921
- Switching from positive to negative axial thermal expansion in two organic crystalline compounds with similar packing. Lalita Negi, Ashutosh Shrivastava, Dinabandhu Das
, Chem. Commun.
, 2018
, 54
, 10675
- Molecular properties in solution described with a continuum solvation model. Jacopo Tomasi, Roberto Cammi, Benedetta Mennucci, Chiara Cappelli, Stefano Corni
, Phys. Chem. Chem. Phys.
, 2002
, 4
, 5697
- Diastereoselective synthesis of half-sandwich chiral-at-metal cobaltacycles by oxidative cyclisation. Jahangir Amin, Christopher J. Richards
, Chem. Commun.
, 2012
, 48
, 10192
- Synthesis and properties of novel 2′-C,4′-C-ethyleneoxy-bridged 2′-deoxyribonucleic acids with exocyclic methylene groups. Takashi Osawa, Satoshi Obika, Yoshiyuki Hari
, Org. Biomol. Chem.
, 2016
, 14
, 9481
- Structure determination, correction, and disproof of marine macrolide natural products by chemical synthesis. Haruhiko Fuwa
, Org. Chem. Front.
, 2021
, 8
, 3990
- Synthesis of (−) cephalosporolide E and (+) cephalosporolide F utilizing the vinylogous Mukaiyama type reaction with an α-chloro sulfide. Sadagopan Raghavan, Javed Sardar Patel, K. V. S. Ramakrishna
, RSC Adv.
, 2016
, 6
, 72877
- The first enantioselective total synthesis of the anti-Helicobacter pylori agent (+)-spirolaxine methyl ether. James E. Robinson, Margaret A. Brimble
, Chem. Commun.
, 2005
, 1560
- Gold-catalyzed heterocyclic syntheses through α-imino gold carbene complexes as intermediates. Enrique Aguilar, Javier Santamaría
, Org. Chem. Front.
, 2019
, 6
, 1513