✦ LIBER ✦

ChemInform Abstract: Addition of Carbon Nucleophiles to Substituted N-Acyliminium Ions. A Stereoselective Route to trans-Fused Decahydroquinoline Systems

✍ Scribed by Adriano O. Maldaner; Ronaldo A. Pilli

Publisher: John Wiley and Sons
Year: 2000
Weight: 28 KB
Volume: 31
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200052123

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Stereoselective Acc

ChemInform Abstract: Stereoselective Access to trans-2,5-Disubstituted Pyrrolidine Derivatives by Nucleophilic Addition to Bicyclic N-Acyliminium Ion.

✍ H. DHIMANE; C. VANUCCI; G. LHOMMET 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 1 views

ChemInform Abstract: Addition of Silylat

ChemInform Abstract: Addition of Silylated Carbon Nucleophiles to Iminium and Cyclic N-Acyliminium Ions Promoted by InCl3.

✍ Dennis Russowsky; Rogerio Zen Petersen; Marla Narciso Godoi; Ronaldo Aloise Pill 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 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

ChemInform Abstract: Highly Stereoselect

ChemInform Abstract: Highly Stereoselective trans Addition of π-Type Nucleophiles to a Bicyclic N-Acyliminium Ion — Application to the Synthesis of Indolizidine and Pyrrolizidine Alkaloids.

✍ H. DHIMANE; C. VANUCCI-BACQUE; L. HAMON; G. LHOMMET 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views

ChemInform Abstract: Nucleophilic Additi

ChemInform Abstract: Nucleophilic Addition of Potassium Organotrifluoroborates to Chiral Cyclic N-Acyliminium Ions: Stereoselective Synthesis of Functionalized N-Heterocycles.

✍ Adriano S. Vieira; Fernando P. Ferreira; Pedro F. Fiorante; Rafael C. Guadagnin; 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 34 KB

Highly Stereoselective trans Addition of

Highly Stereoselective trans Addition of π-Type Nucleophiles to a Bicyclic N-Acyliminium Ion – Application to the Synthesis of Indolizidine and Pyrrolizidine Alkaloids

✍ Hamid Dhimane; Corinne Vanucci-Bacqué; Louis Hamon; Gérard Lhommet 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 446 KB 👁 1 views

Enantiopure bicyclic 5-ethoxytetrahydropyrrolo[1,2-c]oxa-disubstituted pyrrolidines was illustrated by formal syntheses of 3,5-disubstituted indolizidine toxins, starting from 5-zol-3-one 1b was prepared in two steps from the known tosylate 4, which is readily available from (S)-pyroglutamic allylte

ChemInform Abstract: Stereocontrolled Ad

ChemInform Abstract: Stereocontrolled Addition of π-Type Nucleophiles to a Bicyclic N-Acyliminium Ion. New Access to trans-2,6-Disubstituted Piperidine Substructures.

✍ M. DAVID; H. DHIMANE; C. VANUCCI-BACQUE; G. LHOMMET 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views