𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The nitro-aldol reaction of α-ketoaldehydes with nitroalkanes yields α-diketones

✍ Scribed by Konstantinos S. Petrakis; Günes Batu; Josef Fried

Publisher
Elsevier Science
Year
1983
Tongue
French
Weight
111 KB
Volume
24
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Phenylation Reactio
ChemInform Abstract: Phenylation Reaction of α-Acylnitromethanes to Give 1,2-Diketone Monooximes: Involvement of Carbon Electrophile at the Position α to the Nitro Group.
✍ Mikihiro Takamoto; Hiroaki Kurouchi; Yuko Otani; Tomohiko Ohwada 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Highly Enantio- and Diastereoselective O
Highly Enantio- and Diastereoselective Organocatalytic Domino Michael-Aldol Reactions of β-Diketone and β-Ketosulfone Nucleophiles with α,β-Unsaturated Ketones
✍ Juha Pulkkinen; Pompiliu S. Aburel; Nis Halland; Karl Anker Jørgensen 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 97 KB 👁 2 views

## Abstract A chiral imidazolidine catalyst was shown to catalyze the highly enantio‐ and diastereoselective domino Michael‐aldol reaction of β‐diketone and β‐ketosulfone derivatives with α,β‐unsaturated ketones to form optically active cyclohexanones having three or four contiguous chiral centers.