Synthetic studies towards NG-121: Diastereoselective synthesis of NG-121 methyl ether

Synthesis (Germany)

Volumn 44, Issue 24, 2012, Pages 3797-3804

  Singh, Mandeep ^a   Argade, Narshinha P ^a  

^a NATIONAL CHEMICAL LABORATORY   (India)

Author keywords

4 bromo 3,5 dihydroxybenzoate; formylation; intramolecular cyclization; lactonization; NG 121 methyl ether; Stille coupling

Indexed keywords

4-BROMO-3,5-DIHYDROXYBENZOATE; FORMYLATION; INTRAMOLECULAR CYCLIZATIONS; LACTONIZATION; METHYL ETHERS; STILLE COUPLING;

CYCLIZATION; ORGANIC COMPOUNDS; PHENOLS; STEREOSELECTIVITY;

ETHERS;

2 [4,8 DIMETHYLNONA 3,7 DIEN 1 YL] 3 HYDROXY 5 METHOXY 2 METHYL 3,4 DIHYDRO 2H FURO [3,4 H]CHROMEN 7 (9H) ONE METHYL ETHER; 2 [4,8 DIMETHYLNONA 3,7 DIEN 1 YL] 5 METHOXY 3 (METHOXYMETHOXY) 2 METHYL 3,4 DIHYDRO 2H FURO [3,4 H]CHROMEN 7 (9H)ONE; 2 [4,8 DIMETHYLNONA 3,7 DIEN 1 YL] N,N DIETHYL 3 HYDROXY 5 METHOXY 2 METHYL 3,4 DIHYDRO 2H CHROMENE 7 CARBOXAMIDE; 2 [4,8 DIMETHYLNONA 3,7 DIEN 1 YL] N,N DIETHYL 5 METHOXY 3 (METHOXYMETHOXY) 2 METHYL 3,4 DIHYDRO 2H CHROMENE 7 CARBOXAMIDE; 2 [4,8 DIMETHYLNONA 3,7 DIEN 1 YL] N,N DIETHYL 8 FORMYL 5 METHOXY 3 (METHOXYMETHOXY) 2 METHYL 3,4 DIHYDRO 2H CHROMENE 7 CARBOXAMIDE; 3,5 BIS(METHOXYMETHOXY) 4 [3,7,11 TRIMETHYLDODECA 2,6,10 TRIEN 1 YL]BENZALDEHYDE; 4 BROMO 3 METHOXY 5 (METHOXYMETHOXY)BENZOIC ACID; 4 BROMO N,N DIETHYL 3 METHOXY 5 (METHOXYMETHOXY)BENZAMIDE; 4,6 BIS(METHOXYMETHOXY) 5 [3,7,11 TRIMETHYLDODECA 2,6,10 TRIEN 1 YL]ISOBENZOFURAN; 4,6 DIHYDROXY 5 [3,7,11 TRIMETHYLDODECA 2,6,10 TRIEN 1 YL]ISOBENZOFURAN 1 (3H) ONE; [3,5 BIS(METHOXYMETHOXY) 4 [3,7,11 TRIMETHYLDODECA 2,6,10 TRIEN 1 YL]PHENYL]METHANOL; N,N DIETHYL 2 FORMYL 3,5 BIS(METHOXYMETHOXY) 4 [3,7,11 TRIMETHYLDODECA 2,6,10 TRIEN 1 YL]BENZAMIDE; N,N DIETHYL 3 HYDROXY 5 METHOXY 4 [3,7,11 TRIMETHYLDODECA 2,6,10 TRIEN 1 YL]BENZAMIDE; N,N DIETHYL 3 METHOXY 5 (METHOXYMETHOXY) 4 [3,7,11 TRIMETHYLDODECA 2,6,10 TRIEN 1 YL]BENZAMIDE; N,N DIETHYL 3,5 BIS(METHOXYMETHOXY) 4 [3,7,11 TRIMETHYLDODECA 2,6,10 TRIEN 1 YL]BENZAMIDE; NG 121; NOOTROPIC AGENT; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ANTIFUNGAL ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CYCLIZATION; DRUG STRUCTURE; EPOXIDATION; HIGH RESOLUTION MELTING ANALYSIS; HYDROFORMYLATION; NUCLEAR OVERHAUSER EFFECT; POLYMERIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; STACHYBOTRYS; STACHYBOTRYS PARVISPORA; STEREOCHEMISTRY; STILLE REACTION; SYNTHESIS;

EID: 84870883167     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0032-1317544     Document Type: Article

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