Asymmetric total synthesis of erythromycin. 3. Total synthesis of erythromycin


Autoria(s): Woodward, RB; Logusch, E; Nambiar, KP; Sakan, K; Ward, DE; Au-Yeung, BW; Balaram, Padmanabhan
Data(s)

1981

Resumo

In the preceding paper' we described the preparation of the key lactone intermediate la in optically active form. In this paper we report the synthesis of erythromycin (2) from la. In essence,this transformation involves the glycosidation of a suitable derivative of la with L-cladinose and D-desosamine and the generation of the C-9 ketone functionality.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/25681/1/62.pdf

Woodward, RB and Logusch, E and Nambiar, KP and Sakan, K and Ward, DE and Au-Yeung, BW and Balaram, Padmanabhan (1981) Asymmetric total synthesis of erythromycin. 3. Total synthesis of erythromycin. In: Journal of the American Chemical Society, 103 (11). 3215 -3217.

Publicador

American Chemical Society

Relação

http://pubs.acs.org/doi/abs/10.1021/ja00401a051?prevSearch=Asymmetric%2Btotal%2Bsynthesis%2Bof%2Berythromycin.%2B2.%2BSynthesis%2Bof%2Ban%2Berythronolide%2BA%2Blactone%2Bsystem&searchHistoryKey=

http://eprints.iisc.ernet.in/25681/

Palavras-Chave #Molecular Biophysics Unit
Tipo

Editorials/Short Communications

PeerReviewed