Synthesis of an azide-bearing N-mustard analogue of S-adenosyl-L-methionine

Journal of Organic Chemistry

Volumn 76, Issue 24, 2011, Pages 10319-10324

  Mai, Van ^a   Comstock, Lindsay R ^a  

^a WAKE FOREST UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO GROUP; ARYL AZIDES; AZIDATION; BIOCHEMICAL TOOLS; DEOXYADENOSINE; ISOPROPYLIDENE; LATE STAGE; S ADENOSYL L METHIONINES;

ALKYLATION; SUGARS;

AMINO ACIDS;

5' PHTHALIMIDE 5' DEOXY 2',3' BIS (O TRIETHYLSILYL) ADENOSINE; 8 AZIDO 5' (DIAMINOBUTYRIC ACID) N IODOETHYL 5' DEOXYADENOSINE; 8 AZIDO 5' (DIAMINOBUTYRIC ACID) N IODOETHYL 5' DEOXYADENOSINE AMMONIUM; 8 AZIDO 5' (N TERT BUTYLOXYCARBONYL DIAMINOBUTYRIC ACID O TERT BUTYL ESTER) N ETHANOLAMINE 5' DEOXY 2',3' BIS (O TERT BUTYLDIMETHYLSILYL) ADENOSINE; 8 AZIDO 5' (N TERT BUTYLOXYCARBONYL DIAMINOBUTYRIC ACID O TERT BUTYL ESTER) N ETHANOLAMINE 5' DEOXY 2',3' BIS (O TRIETHYLSILYL) ADENOSINE; 8 AZIDO 5' AMINE 5' DEOXY 2',3' BIS (O TRIETHYLSILYL) ADENOSINE; 8 AZIDO 5' N TERT BUTYLOXYCARBONYL DIAMINOBUTYRIC ACID O TERT BUTYL ESTER 5' DEOXY 2',3' BIS (O TRIETHYLSILYL) ADENOSINE; 8 AZIDO 5' PHTHALIMIDE 5' DEOXY 2',3' BIS (O ISOPROPYLIDENE) ADENOSINE; 8 AZIDO 5' PHTHALIMIDE 5' DEOXY 2',3' BIS (O TRIETHYLSILYL) ADENOSINE; 8 BROMO 5' (N TERT BUTYLOXYCARBONYL DIAMINOBUTYRIC ACID O TERT BUTYL ESTER) N ETHANOLAMINE 5' DEOXY 2',3' BIS (O TERT BUTYLDIMETHYLSILYL) ADENOSINE; 8 BROMO 5' ETHANOLAMINE 5' DEOXY 2',3' BIS (O TERT BUTYLDIMETHYLSILYL) ADENOSINE; 8 BROMO 5' PHTHALIMIDE 5' DEOXY 2',3' BIS (O ISOPROPYLIDENE) ADENOSINE; AZIDE; RIBOSE; S ADENOSYLMETHIONINE; UNCLASSIFIED DRUG;

ALKYLATION; AMINATION; ARTICLE; AZIDATION; BROMINATION; CHEMICAL MODIFICATION; DEPROTECTION REACTION; DRUG SYNTHESIS; IODINATION; METHYLATION; REACTION TIME;

ALKYLATION; AZIDES; CHEMISTRY TECHNIQUES, SYNTHETIC; DEOXYADENOSINES; DNA; DNA (CYTOSINE-5-)-METHYLTRANSFERASE; HUMANS; METHYLATION; MOLECULAR PROBES; MUSTARD COMPOUNDS; RIBOSE; S-ADENOSYLMETHIONINE;

EID: 84055190948     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo2019637     Document Type: Article

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