✦ LIBER ✦

ChemInform Abstract: Diastereoselective Reduction of Cyclic Imines and β-Enamino Esters.

✍ Scribed by THANH GIANG VO THANH GIANG VO; J.-P. CELERIER; A. FLEURANT; C. GRANDJEAN; S. ROSSET; G. LHOMMET

Book ID: 112040117
Publisher: John Wiley and Sons
Year: 2010
Weight: 30 KB
Volume: 27
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199646129

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Diastereoselective Reduction of Cyclic I

Diastereoselective Reduction of Cyclic Imines and b-Enamino Esters

✍ Lhommet, Gérard; Vo Thanh, Giang; Célérier, Jean-Pierre; Fleurant, Anne; Grandje 📂 Article 📅 1996 🏛 Japan Institute of Heterocyclic Chemistry 🌐 English ⚖ 94 KB

ChemInform Abstract: Chiral Cyclic β-Ami

ChemInform Abstract: Chiral Cyclic β-Amino Esters. Part 2. Synthesis by Diastereoselective Reduction of Enamino Esters.

✍ J. BLOT; A. BARDOU; C. BELLEC; M.-C. FARGEAU-BELLASOUED; J. P. CELERIER; G. LHOM 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

Chiral cyclic β-amino esters. Part II: S

Chiral cyclic β-amino esters. Part II: Synthesis by diastereoselective reduction of enamino esters

✍ J. Blot; A. Bardou; C. Bellec; M.-C. Fargeau-Bellassoued; J.P. Célérier; G. Lhom 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 182 KB

Catalytic and chemical reductions of chiral pyrrolidine 13-enamino esters provides corresponding [3-amino esters with good to moderate diastereomer excesses. The unexpected major diastereomer 5 comes from a reduction process which amounts to an anti hydrogen addition.

ChemInform Abstract: Highly Diastereosel

ChemInform Abstract: Highly Diastereoselective Addition of Cyclic β-Enamino Esters to N-Acryloyl-(S)-proline Derivatives.

✍ K. HERVOUET; A. GUINGANT 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB

Cyclic β-enamino esters dialkylation: A

Cyclic β-enamino esters dialkylation: A new route to cyclic imines

✍ Marina Eugene; Jean-Pierre Celerier; Nello Ronzani; Gérard Lhommet 📂 Article 📅 1993 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 214 KB

Chiral heterocyclic β-enamino esters: co

Chiral heterocyclic β-enamino esters: convenient synthesis and diastereoselective reduction

✍ Sandrine Calvet; Olivier David; Corinne Vanucci-Bacqué; Marie-Claude Fargeau-Bel 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 205 KB

The preparation of chiral pyrrolidine and piperidine b-enamino esters starting from v-halogeno b-keto esters, their diastereoselective reduction and the subsequent cleavage of the chiral auxiliary are described.