Synthesis of an (R)-Garner-type aldehyde from L-serine: Useful building block for a (+)-furanomycin derivative

Synthesis

Volumn , Issue 6, 2009, Pages 951-956

  Bartoli, Giuseppe ^a   Di Antonio, Giustino ^b   Fiocchi, Roberto ^c   Giuli, Sandra ^c   Marcantoni, Enrico ^c   Marcolini, Mauro ^c  

^a UNIVERSITY OF BOLOGNA   (Italy)

^b Boehringer Ingelheim Italia SpA   (Italy)

^c UNIVERSITY OF CAMERINO   (Italy)

Author keywords

Amino acids; Diastereoselectivity; Lanthanides; Natural products; Protecting groups; Wittig reactions

Indexed keywords

DIASTEREOSELECTIVITY; LANTHANIDES; NATURAL PRODUCTS; PROTECTING GROUPS; WITTIG REACTIONS;

ALDEHYDES; AMINATION; AMINES; CARBOXYLIC ACIDS; GROUP TECHNOLOGY; NITROGEN COMPOUNDS; ORGANIC ACIDS; RARE EARTH ELEMENTS;

AMINO ACIDS;

2 AMINO 3 (TERT BUTYLDIMETHYLSILOXY)PROPAN 1 OL; ALDEHYDE DERIVATIVE; ANTIBIOTIC AGENT; CARBOXYLIC ACID; FURAN DERIVATIVE; SERINE; TERT BUTYL 3 (HYDROXYMETHYL) 1 OXA 4 AZASPIRO(4.5)DECANE 4 CARBOXYLATE; TERT BUTYL 3 [ 1 HYDROXYALLYL] 1 OXA 4 AZA SPIRO(4.5)DECANE 4 CARBOXYLATE(SYN 14); TERT BUTYL 3 [ 1 HYDROXYALLYL] 1 OXA 4 AZASPIRO(4.5)DECANE 4 CARBOXYLATE(ANTI 14); TERT BUTYL 3 FORMYL 1 OXA 4 AZASPIRO(4.5)DECANE 4 CARBOXYLATE; TERT BUTYL 3 VINYL 1 OXA 4 AZASPIRO(4.5)DECANE 4 CARBOXYLATE; TERT BUTYL N[2 (TERT BUTYLDIMETHYLSILOXY) 1 (HYDROXYMETHYL)ETHYL]CARBAMATE; TERT BUTYL N[2,2 DIMETHYL 4 VINYL 1,3 DIOXAN 5 YL]CARBAMATE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL MODIFICATION; DRUG DETERMINATION; DRUG SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE; REDUCTION; SUBSTITUTION REACTION;

EID: 67649535362     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0028-1087851     Document Type: Article

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