Remarkably Stable Tetrahedral Intermediates: Carbinols from Nucleophilic Additions to N‐Acylpyrroles.
Cited by 2
Related Papers
Directed reduction of .beta.-hydroxy ketones employing tetramethylammonium triacetoxyborohydride
|Journal of the American Chemical Society|1988|945
Remarkably Stable Tetrahedral Intermediates: Carbinols from Nucleophilic Additions to<i>N</i>���Acylpyrroles
|Angewandte Chemie International Edition|2002|167
One-pot asymmetric synthesis of tert-butanesulfinyl-protected amines from ketones by the in situ reduction of tert-butanesulfinyl ketimines
|Tetrahedron Letters|1999|111
Asymmetric synthesis of pre-protected α,α-disubstituted amino acids from tert-butanesulfinyl ketimines
|Tetrahedron Letters|2001|77
Naphthamides as Novel and Potent Vascular Endothelial Growth Factor Receptor Tyrosine Kinase Inhibitors: Design, Synthesis, and Evaluation
|Journal of Medicinal Chemistry|2008|70