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Titolo:
SYNTHESIS OF SEGMENT-C OF TAUTOMYCIN
Autore:
JIANG YM; ICHIKAWA Y; ISOBE M;
Indirizzi:
NAGOYA UNIV,SCH AGR SCI,ORGAN CHEM LAB,CHIKUSA KU NAGOYA AICHI 46401 JAPAN NAGOYA UNIV,SCH AGR SCI,ORGAN CHEM LAB,CHIKUSA KU NAGOYA AICHI 46401 JAPAN
Titolo Testata:
Synlett
fascicolo: 3, , anno: 1995,
pagine: 285 - 288
SICI:
0936-5214(1995):3<285:SOSOT>2.0.ZU;2-Z
Fonte:
ISI
Lingua:
ENG
Soggetto:
MARINE TOXIC POLYETHERS; OKADAIC ACID; STEREOCONTROLLED SYNTHESIS; SILYLACETYLENES; REDUCTION; GLUCALS;
Keywords:
TAUTOMYCIN; SEGMENT C; HETEROCONJUGATE ADDITION; PSEUDOENANTIOMER; ENANTIOMER; SULFONE;
Tipo documento:
Note
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Citazioni:
29
Recensione:
Indirizzi per estratti:
Citazione:
Y.M. Jiang et al., "SYNTHESIS OF SEGMENT-C OF TAUTOMYCIN", Synlett, (3), 1995, pp. 285-288

Abstract

Synthesis of Segment C of tautomycin was accomplished from 2 D-sugar derivatives. New heteroconjugate addition strategy allowed stereocontrolled syntheses of the 2 sub-segments, C-1 and C-2, and 3 other diastereoisomers of the latter. Sub-segments were coupled between sulfone carbanion and epoxide electrophile to furnish the spiro ring moiety of the target compound.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 14/07/20 alle ore 19:20:35