Expeditious synthesis of enantiopure symmetrical macroheterocycles by ring-closing metathesis of ether and tether-linked 1,2-O- isopropylidenefuranosides

Carbohydrate Research

Volumn 340, Issue 4, 2005, Pages 567-578

  Biswas, Goutam ^a   Sengupta, Jhimli ^a   Nath, Madhumita ^a   Bhattacharjya, Anup ^a  

^a INDIAN INSTITUTE OF CHEMICAL BIOLOGY   (India)

Author keywords

Enantiopure; Macroheterocycles; Ring closing metathesis; Synthesis; Tether linked 1,2 O isopropylidenefuranosides

Indexed keywords

CATALYSTS; OLEFINS; SUBSTRATES; SUGARS; SYNTHESIS (CHEMICAL);

ETHER LINKAGE; EXPENDITIOUS SYNTHESIS; MACROHETEROCYCLES; RING-CLOSING METATHESIS (RCM);

ETHERS;

(2,3:21,22 DIISOPROPYLIDENEDIOXY 2,3,5,3A,20A,21,22,23A OCTAHYDRODIBENZO[C,J]DIFURO[2,3 C:3,2 R][1,5,9,13,17,21]HEXAOXACYCLOPENTACOSA 7A,14A,20A,27,31A PENTAENE; (3,4:12,13 DIISOPROPYLIDENEDIOXY) 1,10 BIS(1,2 ISOPROPYLIDENEDIOXYETHYL) 2,6,8,11 TETRAOXADISPIRO[4.3.4.4]HEPTADEC 15 ENE; (6,7:20,21 DIISOPROPYLIDENEDIOXY) 2,4,8,11,16,19 HEXAOXATRICYCLO[16.3.0.0 5,9 ]HENEICOS 13 ENE; (6,7:20,21 DIISOPROPYLIDENEDIOXY) 2,4,8,11,16,19 HEXAOXATRICYCLO[16.3.0.0 5,9 ]HENEICOSANE; (7,8:17,18 DIISOPROPYLIDENEDIOXY) 3,6,10,15,19 PENTAOXATRICYCLO[14.3.0.0 5,9 ]NONADEC 12 ENE; (9,10:19,20 DIISOPROPYLIDENEDIOXY) 3,5,8,12,17,21 HEXAOXATRICYCLO[16.3.0.0 7,11 ]HENEICOS 14 ENE; 2,3:21,22 DIISOPROPYLIDENEDIOXY 2,3,3A,20A,21,22,23A,25A OCTAHYDRODIBENZO[C,J]DIFURO[2,3 N:3,2 R][1,5,9,13]TETRAOXACYCLONONADECA 5A,14A,20A,24,25A PENTAENE; 8,9:22,23 DIISOPROPYLIDENEDIOXY 2,6 BIS(4 TOLUENESULFONYL) 10,13,18,21 TETRAOXA 2,6 DIAZATRICYCLO[18.3.0.0 7,11 ]TRICOS 15 ENE; CARBOHYDRATE DERIVATIVE; ETHER; FURAN DERIVATIVE; HETEROCYCLIC COMPOUND; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYST; CHEMICAL COMPOSITION; DRUG SYNTHESIS; MASS SPECTROMETRY; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; RING CLOSING METATHESIS; STRUCTURE ANALYSIS;

CYCLIZATION; ETHERS; HETEROCYCLIC COMPOUNDS; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION; PENTOSES; STEREOISOMERISM;

EID: 13844310307     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2004.12.024     Document Type: Article

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