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| 001 | 281034 | ||
| 005 | 20210129221607.0 | ||
| 024 | 7 | _ | |a 10.1002/ejoc.201500700 |2 doi |
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| 100 | 1 | _ | |a Eichenauer, Nils C. |0 P:(DE-HGF)0 |b 0 |
| 245 | _ | _ | |a Total Synthesis of Solandelactones A and B |
| 260 | _ | _ | |a Weinheim |c 2015 |b Wiley-VCH Verl. |
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| 520 | _ | _ | |a The total synthesis of solandelactones A and B is presented. The eastern cyclopropyl moiety was prepared following an exceptionally short chemoenzymatic approach whereas enantioselective synthesis of the western side-chain relied on the application of diastereomerically pure allyl boronates. The natural products solandelactones A and B were isolated in good overall yields following convergence of each eastern and western element by application of the Nozaki–Hiyama–Kishi reaction. |
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| 700 | 1 | _ | |a Nordschild, Anja C. M. |0 P:(DE-HGF)0 |b 1 |
| 700 | 1 | _ | |a Bischop, Martina |0 P:(DE-HGF)0 |b 2 |
| 700 | 1 | _ | |a Schumacher, Dominik |0 P:(DE-HGF)0 |b 3 |
| 700 | 1 | _ | |a Mackwitz, Marcel K. W. |0 P:(DE-HGF)0 |b 4 |
| 700 | 1 | _ | |a Tschersich, Roxanne |0 P:(DE-HGF)0 |b 5 |
| 700 | 1 | _ | |a Wilhelm, Thorsten |0 P:(DE-HGF)0 |b 6 |
| 700 | 1 | _ | |a Pietruszka, Jörg |0 P:(DE-Juel1)128906 |b 7 |e Corresponding author |u fzj |
| 773 | _ | _ | |a 10.1002/ejoc.201500700 |g Vol. 2015, no. 25, p. 5620 - 5632 |0 PERI:(DE-600)1475010-7 |n 25 |p 5620 - 5632 |t European journal of organic chemistry |v 2015 |y 2015 |x 1434-193X |
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