A one-pot, three-step process for the diastereoselective synthesis of aminobicyclo[4.3.0]nonanes using consecutive palladium(II)- and ruthenium(II)-catalysis

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A one-pot, three-step process for the diastereoselective synthesis of aminobicyclo[4.3.0]nonanes using consecutive palladium(II)- and ruthenium(II)-catalysis is …
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scholarly articleQ13442814

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P356DOI10.1039/C6OB00165C
P8608Fatcat IDrelease_gfphqctvrzgt5mnkqfcdiyfhfe
P698PubMed publication ID26932788

P50authorAndrew SutherlandQ43080825
P2093author name stringClaire Wilson
Mohamed A B Mostafa
Mark W Grafton
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ASYMMETRIC REARRANGEMENT OF ALLYLIC TRICHLOROACETIMIDATES: PREPARATION OF (S)-2,2,2-TRICHLORO-N-(1-PROPYLALLYL)ACETAMIDEQ57636378
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Diastereoselective synthesis of highly substituted polycyclic scaffolds via a one-pot four-step tandem catalytic processQ58856798
A three-step tandem process for the synthesis of bicyclic γ-lactamsQ58856859
P433issue12
P921main subjectdiastereoselectivityQ64131393
P304page(s)3284-3297
P577publication date2016-03-02
P1433published inOrganic and Biomolecular ChemistryQ3355939
P1476titleA one-pot, three-step process for the diastereoselective synthesis of aminobicyclo[4.3.0]nonanes using consecutive palladium(II)- and ruthenium(II)-catalysis
P478volume14

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cites work (P2860)
Q57717105Highly Enantioselective One-Pot Synthesis of Chiral β-Heterosubstituted Alcohols via Ruthenium–Prolinamide-Catalyzed Asymmetric Transfer Hydrogenation
Q48110758Structural diversification of the aminobicyclo[4.3.0]nonane skeleton using alkynylsilyl-derived allylic trichloroacetimidates

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