Improved alkylation and product stability in phosphotriester formation through quinone methide reactions with dialkyl phosphates

Journal of Organic Chemistry

Volumn 70, Issue 11, 2005, Pages 4338-4345

  Bakke, Brian A ^a   McIntosh, Matthias C ^a   Turnbull, Kenneth D ^a  

^a UNIVERSITY OF ARKANSAS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; ESTERS; HYDROLYSIS; IONIZATION; ORGANIC COMPOUNDS; PHOSPHORUS COMPOUNDS; REACTION KINETICS; STABILITY;

HYDROLYSIS PRODUCTS; LACTIONIZATION; PRODUCT STABILITY; TRIALKYL PHOSPHATE;

ALKYLATION;

3 [3 (2 TERT BUTOXYCARBONYLAMINOETHYL) 6 HYDROXY 2,5 DIMETHYLPHENYL]PROPIONIC ACID METHYL ESTER; 3 [5 (2 TERT BUTOXYCARBONYLAMINOETHYL) 2 HYDROXY 3 METHYLPHENYL]PROPIONIC ACID METHYL ESTER; CATECHOL DERIVATIVE; ESTER DERIVATIVE; LACTONE DERIVATIVE; ORGANOPHOSPHATE; PHENOL DERIVATIVE; QUINONE DERIVATIVE; QUINONE METHIDE DERIVATIVE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CONFORMATION; HYDROLYSIS; ORGANIC CHEMISTRY; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; ULTRAVIOLET SPECTROSCOPY;

ALKYLATION; DNA; LACTONES; MAGNETIC RESONANCE SPECTROSCOPY; ORGANOPHOSPHORUS COMPOUNDS; OXIDATION-REDUCTION; PHOSPHORIC ACID ESTERS; QUINONES;

EID: 19544394259     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo050050s     Document Type: Article

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