Regio- and stereoselective reduction of bicyclic imides for the asymmetric synthesis of highly substituted pyrrolidines

Tetrahedron

Volumn 49, Issue 18, 1993, Pages 3781-3792

  Deprez, Pierre ^a   Royer, Jacques ^a   Husson, Henri Philippe ^a  

^a INSTITUT DE CHIMIE DES SUBSTANCES NATURELLES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

PYRROLIDINE DERIVATIVE;

ARTICLE; REACTION ANALYSIS; SYNTHESIS;

EID: 0027230345     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)90230-3     Document Type: Article

References (34)

1. α-Amidoalkylation at Carbon: Recent Advances - Part I
2. .omega.-Alkoxy lactams as dipolar synthons. Silicon-assisted synthesis of azabicycles and a .gamma.-amino acid
3. Intramolecular N-(acyloxy)iminium ion-alkyne cycloadditions. A new route to bicyclic .alpha.-amino ketones
4. Synthesis of 1,5-Dienes and 6-Azabicyclo[3.2.1]octanes via w-Carbinollactams
5. 1,2-Asymmetric induction in intramolecular Michael reaction. A novel and enantioselective route to (+)-Geissman lactone
6. Synthese von 15,16-Dimethoxy-8-oxo-cis-erythrinan-6-carbons�ure�thylester
7. Synthesis and Stereochemistry of Some 3,6-Disubstituted 2-Oxopiperidines
8. A Novel Reductive Cyclization of Imides
9. Applications of Diisobutylaluminium Hydride (DIBAH) and Triisobutylaluminium (TIBA) as Reducing Agents in Organic Synthesis