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Titolo:
Radical cyclization of beta-aminoacrylates: Synthesis of (-)-indolizidine 223AB
Autore:
Lee, E; Jeong, EJ; Min, SJ; Hong, S; Lim, J; Kim, SK; Kim, HJ; Choi, BG; Koo, KC;
Indirizzi:
Seoul Natl Univ, Sch Chem & Mol Engn, Seoul 151742, South Korea Seoul NatlUniv Seoul South Korea 151742 Engn, Seoul 151742, South Korea
Titolo Testata:
ORGANIC LETTERS
fascicolo: 14, volume: 2, anno: 2000,
pagine: 2169 - 2171
SICI:
1523-7060(20000713)2:14<2169:RCOBSO>2.0.ZU;2-6
Fonte:
ISI
Lingua:
ENG
Soggetto:
STEREOSELECTIVE SYNTHESIS; OXACYCLE SYNTHESIS; FORMAL SYNTHESIS; ALKOXYACRYLATES; ALKALOIDS; REAGENT; ETHERS; 195B;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Physical, Chemical & Earth Sciences
Citazioni:
26
Recensione:
Indirizzi per estratti:
Indirizzo: Lee, E Seoul Natl Univ, Sch Chem & Mol Engn, Seoul 151742, South Korea Seoul Natl Univ Seoul South Korea 151742 eoul 151742, South Korea
Citazione:
E. Lee et al., "Radical cyclization of beta-aminoacrylates: Synthesis of (-)-indolizidine 223AB", ORG LETT, 2(14), 2000, pp. 2169-2171

Abstract

[GRAPHICS](-)-Indolizidine 223AB was synthesized via radical cyclization of the beta-aminoacrylate derivative of a trans-2,5-disubstituted pyrrolidine. The trans-2,5-disubstituted pyrrolidine substrate was prepared by radical cyclization of a Ses protected beta-aminoacrylate.

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Documento generato il 25/11/20 alle ore 06:37:16