Chemoselective coupling reactions of 5,7-dimethoxyphthalide with the remotely functionalized alkyl iodides: Facile racemic synthesis of helicobacter pylori antibiotics

Journal of Organic Chemistry

Volumn 75, Issue 9, 2010, Pages 3121-3124

  Singh, Mandeep ^a   Argade, Narshinha P ^a  

^a NATIONAL CHEMICAL LABORATORY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ALKYL IODIDES; CHEMOSELECTIVE COUPLING; EFFICIENT SYNTHESIS; FUNCTIONALIZED; HELICOBACTER PYLORI; LONG CHAINS; METHYL ETHERS;

ALKYLATION; ETHERS; SYNTHESIS (CHEMICAL);

ANTIBIOTICS;

5,7 DIMETHOXYPHTHALIDE; ACETOACETIC ACID; ANTIBIOTIC AGENT; CARBON; ETHYL 2 ACETYL 13 (4,6 DIMETHOXY 3 OXO 1,3 DIHYDROISOBENZOFURAN 1 YL)TRIDECANOATE; IODINE DERIVATIVE; PHTHALIDE DERIVATIVE; UNCLASSIFIED DRUG;

ALKYLATION; ANTIBACTERIAL ACTIVITY; ARTICLE; CHEMICAL BOND; DRUG STRUCTURE; DRUG SYNTHESIS; HELICOBACTER PYLORI; NONHUMAN;

ANTI-BACTERIAL AGENTS; BENZOFURANS; CYCLIZATION; HELICOBACTER INFECTIONS; HELICOBACTER PYLORI; HYDROCARBONS, IODINATED; MOLECULAR STRUCTURE; SPIRO COMPOUNDS; STEREOISOMERISM;

EID: 77951772288     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo100168f     Document Type: Article

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