First general route to substituted α-arylamino-α′ chloropropan-2-ones by oxidation of N-protected aminohalohydrins: The importance of disrupting hydrogen bond networks

Synthesis

Volumn , Issue 20, 2010, Pages 3545-3555

  Pace, Vittorio ^a   Cabrera, Álvaro Cortés ^b   Fernández, María ^a   Sinisterra, José V ^a,c   Alcántara, Andrés R ^a  

^a UNIVERSIDAD COMPLUTENSE DE MADRID   (Spain)

^b UNIVERSIDAD AUTÓNOMA DE MADRID   (Spain)

^c Industrial Biotransformations Service   (Spain)

Author keywords

amino alcohols; amino ketones; hydrogen bonding; oxidation; protecting groups

Indexed keywords

AMINO ALCOHOLS; AMINO KETONES; COMPUTER MODELING; DESS-MARTIN PERIODINANE; FUNCTIONALIZED; HYDROGEN BOND NETWORKS; HYDROGEN BONDING; INTERMOLECULAR HYDROGEN BONDS; IODOTRIMETHYLSILANE; IR SPECTROSCOPY; PROTECTING GROUP; QUANTITATIVE YIELDS; REGIO-SELECTIVE;

ALCOHOLS; AMINES; HYDROGEN; KETONES; OXIDATION;

HYDROGEN BONDS;

ALPHA ARYLAMINO ALPHA' CHLOROPROPAN 2 ONE; AMINOALCOHOL; AMINOHALOHYDRIN; CARBAMIC ACID DERIVATIVE; IODOTRIMETHYLSILANE; KETONE DERIVATIVE; SILANE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; COMPUTER MODEL; DESS MARTIN OXIDATION; HYDROGEN BOND; INFRARED SPECTROSCOPY;

EID: 77957785439     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1257938     Document Type: Article

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