遷移金属が配位した面不斉アルデヒド，イミンの還元的カップリングによる光学活性β‐ジオール，ジアミン，アミノアルコールの合成

Abstract

Chiral β-diols, diamines and amino alcohols are significantly important compounds in asymmetric reaction. These compounds were prepared by samarium diiodide-mediated reductive coupling of planar chiral transition metal complexes. Planar chiral ortho-substituted benzaldehyde tricarbonyl chromium complexes were treated with samarium diiodide to give optically pure β-diols. Similarly, planar chiral benzaldimine chromium complexes afforded β-diamines in enantiopure form. Furthermore, reductive cross-coupling of planar chiral aldehydes with N-tosyl aldimines gave optically pure β-amino alcohols without formation of homo-coupling products. Thus, samarium diiodide-mediated reductive cross-coupling of N-tosylferrocenylideneamines with planar chiral ferocenecarboxaldehydes or benzaldehyde chromium complexes gave optically pure anti-β-amino alcohols. On the other hand, the reductive cross coupling of N-tosyl benzylideneamines with planar chiral aldehydes afforded optically pure syn-β-amino alcohols.