✦ LIBER ✦

Highly Enantioselective Intramolecular Cyclopropanation Reactions of N -Allylic- N -methyldiazoacetamides Catalyzed by Chiral Dirhodium(II) Carboxamidates

✍ Scribed by Doyle, Michael P.; Kalinin, Alexey V.

Book ID: 120422783
Publisher: American Chemical Society
Year: 1996
Tongue: English
Weight: 248 KB
Volume: 61
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo9519219

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Highly Enantioselec

ChemInform Abstract: Highly Enantioselective Intramolecular Cyclopropanation Reactions of N- Allylic-N-methyldiazoacetamides Catalyzed by Chiral Dirhodium(II) Carboxamidates.

✍ M. P. DOYLE; A. V. KALININ 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB

Enantioselective intramolecular cyclopro

Enantioselective intramolecular cyclopropanation of N-allylic- and N-homoallylic diazoacetamides catalyzed by chiral dirhodium(II) catalysts

✍ Michael P. Doyle; Michail Y. Eismont; Marina N. Protopopova; Michelle M.Y. Kwan 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 648 KB

ChemInform Abstract: Highly Enantioselec

ChemInform Abstract: Highly Enantioselective Route to β-Lactams via Intramolecular C-H Insertion Reactions of Diazoacetylazacycloalkanes Catalyzed by Chiral Dirhodium(II) Carboxamidates.

✍ M. P. DOYLE; A. V. KALININ 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB

ChemInform Abstract: Highly Enantioselec

ChemInform Abstract: Highly Enantioselective Hetero-Diels—Alder Reactions Between Rawal′s Diene and Aldehydes Catalyzed by Chiral Dirhodium(II) Carboxamidates.

✍ Yudai Watanabe; Takuya Washio; Naoyuki Shimada; Masahiro Ananda; Shunichi Hashim 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB 👁 1 views

## 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

A highly regio-, diastereo- and enantios

A highly regio-, diastereo- and enantioselective intramolecular cyclopropanation reaction of a racemic α-diazo ketone catalyzed by chiral ortho-metalated dirhodium(II) compounds

✍ Julia Pérez-Prieto; Salah-Eddine Stiriba; Eduardo Moreno; Pascual Lahuerta 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 110 KB

A series of racemic dirhodium(II) compounds with two ortho-metalated aryl phosphine ligands in a head-to-tail arrangement Rh 2 (O 2 CR) 2 (pc) 2 (pc=ortho-metalated aryl phosphine) (1a-k) were tested in the regio-and stereoselective cyclopropanation of racemic 1-diazo-6-methyl-3-(2-propenyl)-5-hepte

A Highly Regio-, Diastereo- and Enantios

A Highly Regio-, Diastereo- and Enantioselective Intramolecular Cyclopropanation Reaction of a Racemic α-Diazo Ketone Catalyzed by Chiral ortho-Metalated Dirhodium(II) Compounds.

✍ Julia Perez-Prieto; Salah-Eddine Stiriba; Eduardo Moreno; Pascual Lahuerta 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 96 KB 👁 2 views