One important theme in organic synthesis is to accomplish highly selective
transformations under mild conditions, which yield only desirable products.
During the past two decades, we have developed several useful tools to ach
ieve this, i.e., organochromium reagents. This review focuses on the follow
ing themes: 1) The historical background of organochromium reagents. 2) The
development of the allylic chromium reagent (Nozaki-Hiyama reaction). 3) N
ickel-catalyzed addition of alkenyl-, aryl-, and alkynyl halides to aldehyd
es (Nozaki-Hiyama-Kishi (NHK) reaction). 4) Wittig-type olefination with ge
minal dichromium reagents. 5) Representative applications of organochromium
reagents to the total syntheses of biologically active compounds.