Catalytic Asymmetric Hydrophosphonylation of Ketimines
摘要:
Catalytic asymmetric hydrophosphonylation of aromatic and aliphatic N-thiophosphinoyl ketimines with dialkyl phosphite was efficiently promoted by as little as 0.5 mol% of catalyst loading at ambient temperature. The catalyst can be recovered for repeated use, and facile removal of the thiophosphinoyl group allowed for ready access to the phosphonic acid analogue of enantioenriched alpha,alpha-disubstituted alpha-amino acids.
Compound, Manufacturing Method Therefor, and Method for Manufacturing Optically Active alpha-Aminophosphonate Derivative
申请人:MICROBIAL CHEMISTRY RESEARCH FOUNDATION
公开号:US20160145278A1
公开(公告)日:2016-05-26
A method for producing a compound represented by General Formula (1), the method including:
reacting a compound represented by General Formula (3) and a compound represented by General Formula (4):
where R
1
and R
2
each represent aliphatic group which may have substituent, or aromatic group which may have substituent (with the proviso that R
1
and R
2
are different groups), R
3
represents aromatic group which may have substituent, and R
4
represents aliphatic group which may have substituent, or aromatic group which may have substituent,
where R
1
and R
2
each represent aliphatic group which may have substituent, or aromatic group which may have substituent (with the proviso that R
1
and R
2
are different groups), and R
3
represents aromatic group which may have substituent,
where R
4
represents aliphatic group which may have substituent, or aromatic group which may have substituent.