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Published in 2020 at "Mendeleev Communications"
DOI: 10.1016/j.mencom.2020.01.003
Abstract: The title compound, as the new chiral building block for bioactive cyclopentenones, was prepared in 8 steps with 15% overall yield. The key steps involve selective homologation in intermediate [(1S,2R,5R)-5-trimethysilylcyclopent-3-ene- 1,2-diyl]dimethanol by regioselective silylation followed…
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Keywords:
7ar tetrahydrocyclopenta;
convenient synthesis;
enantiopure 4as;
synthesis enantiopure ... See more keywords
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Published in 2022 at "Organic Letters"
DOI: 10.1021/acs.orglett.2c01547
Abstract: Propargylic alcohols and amines are versatile building blocks in organic synthesis. We demonstrate a straightforward enzymatic cascade to synthesize enantiomerically pure propargylic alcohols and amines from readily available racemic starting materials. In the first step,…
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Keywords:
synthesis enantiopure;
alcohols amines;
propargylic alcohols;
platform synthesis ... See more keywords
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Published in 2018 at "Organic chemistry frontiers"
DOI: 10.1039/c7qo00908a
Abstract: The screening of a family of complexes of the formula [RuCl2(R-pybox)(L)] (R-pybox = Ph-, iPr- or indane-pybox; L = monodentate P, N or C ligand) in the enantioselective hydrogenation of N-aryl imines indicates a strong…
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Keywords:
hydrogenation;
practical synthesis;
transfer hydrogenation;
pybox ... See more keywords