Abstract
Development of nucleophilic organometallic species plays an important role in organic synthesis, especially for construction of carbon skeletons. This account describes the following synthetic reactions with novel organometallic species: (1) Preparation of alkenylchromium reagents for chemoselective addition to aldehydes, (2) Generation of geminai dimetallic species of zinc and chromium for the Wittig-type olefination, (3) Preparation of tantalum-alkyne complexes and their synthetic use, (4) Activation and deactivation of zinc with a catalytic amount of lead, (5) Control of one-electron transfer and its application to sequential radical and anionic reactions, (6) Rhenium and manganese catalyzed-Barbier-type addition of aromatic compounds to aldehydes based on C-H bond activation. The account focuses on the background to the research and how the reactions were discovered.
Original language | English |
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Pages (from-to) | 3-18 |
Number of pages | 16 |
Journal | Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry |
Volume | 68 |
Issue number | 1 |
DOIs | |
Publication status | Published - Jan 2010 |
Externally published | Yes |
Keywords
- Activation of metal
- C-H bond activation
- Chemoselective addition
- Chromium
- Manganese
- One-electron transfer
- Rhenium
- Tantalum
- Titanium
- Wittig-type olefination
ASJC Scopus subject areas
- Organic Chemistry