Nucleophilic addition of organochromium reagents to carbonyl compounds

Citation
K. Takai et H. Nozaki, Nucleophilic addition of organochromium reagents to carbonyl compounds, P JPN AC B, 76(8), 2000, pp. 123-131
Citations number
52
Categorie Soggetti
Multidisciplinary
Journal title
PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES
ISSN journal
03862208 → ACNP
Volume
76
Issue
8
Year of publication
2000
Pages
123 - 131
Database
ISI
SICI code
0386-2208(200010)76:8<123:NAOORT>2.0.ZU;2-#
Abstract
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.