Antibacterial pyridines

(R)-(+)-1-Boc-2-pyrrolidinecarbonitrile.

Application：(S)-3-(Boc-amino)pyrrolidine can be used as a building block to prepare:2,4,6-trisubstitued pyrido[3,4-d]pyrimidine derivatives as potent inhibitors against EGFR tyrosine kinase.Aminopyrrolidine scaffolds for asymmetric

Application：(S)-3-(Boc-amino)pyrrolidine can be used as a building block to prepare:2,4,6-trisubstitued pyrido[3,4-d]pyrimidine derivatives as potent inhibitors against EGFR tyrosine kinase.Aminopyrrolidine scaffolds for asymmetric

Application：(S)-3-(Boc-amino)pyrrolidine can be used as a building block to prepare:2,4,6-trisubstitued pyrido[3,4-d]pyrimidine derivatives as potent inhibitors against EGFR tyrosine kinase.Aminopyrrolidine scaffolds for asymmetric

Application：(S)-3-(Boc-amino)pyrrolidine can be used as a building block to prepare:2,4,6-trisubstitued pyrido[3,4-d]pyrimidine derivatives as potent inhibitors against EGFR tyrosine kinase.Aminopyrrolidine scaffolds for asymmetric

Application：(S)-3-(Boc-amino)pyrrolidine can be used as a building block to prepare:2,4,6-trisubstitued pyrido[3,4-d]pyrimidine derivatives as potent inhibitors against EGFR tyrosine kinase.Aminopyrrolidine scaffolds for asymmetric

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

1H‐pyrrolo[2,3‐b]pyridine‐2‐carboxamide.

It has been used to efficiently ortho deprotonate pyridine-3-carboxamides.

It has been used to efficiently ortho deprotonate pyridine-3-carboxamides.

2,4-Pyridinedicarbonitrile.

2,4-Pyridinedicarbonitrile.