Relative reactivity of hydroxyl groups in inositol derivatives: role of metal ion chelation

Carbohydrate Research

Volumn 344, Issue 10, 2009, Pages 1159-1166

  Devaraj, Subramanian ^a   Jagdhane, Rajendra C ^a   Shashidhar, Mysore S ^a  

^a NATIONAL CHEMICAL LABORATORY   (India)

Author keywords

Carbohydrate; Chelation; Cyclitol; Inositol; Protecting group

Indexed keywords

ALKOXIDE; ALKYLATION REACTIONS; CYCLITOL; HYDROXYL GROUPS; INOSITOL; LITHIUM ALKOXIDES; METAL ALKOXIDES; METAL-ION CHELATION; MYO-INOSITOL; OXYGEN ATOM; PROTECTING GROUP; REACTION TEMPERATURE; RELATIVE REACTIVITIES; STERIC FACTOR; SYNTHETIC STRATEGIES;

ALKYLATION; CHELATION; HYDROCARBONS; LITHIUM; METAL IONS; OXYGEN; REGIOSELECTIVITY; SUGARS;

ALCOHOLS;

HYDROXYL GROUP; INOSITOL DERIVATIVE; LITHIUM DERIVATIVE; METAL ION; SODIUM DERIVATIVE;

ALKYLATION; ARTICLE; CHELATION; CHEMICAL REACTION; PRIORITY JOURNAL; SOLVENT EFFECT; TEMPERATURE;

ALKYLATION; CHELATING AGENTS; HYDROXIDES; INOSITOL; METALS, ALKALI; ORGANOMETALLIC COMPOUNDS; SODIUM COMPOUNDS; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

EID: 66649096483     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2009.04.007     Document Type: Article

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