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Rosenberg, I.
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Synthesis of 9-(2-(Phosphonomethoxy)ethyl)adenine and related compounds
ÆÚ¿¯Ãû,Äê·Ý,¾í(ÆÚ),ÆðÖ¹Ò³Âë:
Coll. Czech. Chem. Commun., 1987, 52, 2801-2809
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sunshan4379: ½ð±Ò+2, ¸Ðл»ý¼«»Ø¸´£¡ 2015-09-22 16:41:57
SYNTHESIS OF 9-(2-PHOSPHINOMETHOXYETHYL)ADENINE AND RELATED-COMPOUNDS
×÷Õß:ALEXANDER, P (ALEXANDER, P); HOLY, A (HOLY, A); MASOJIDKOVA, M (MASOJIDKOVA, M)
COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS
¾í: 59  ÆÚ: 8  Ò³: 1870-1878
DOI: 10.1135/cccc19941870
³ö°æÄê: AUG 1994
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Alkyl 2-chloroethoxymethyl(diethoxymethyl)phosphinates VII and XIII were prepared by reaction of silyl esters of dialkoxymethylphosphinic acid with 2-chloroethyl chloromethyl ether. Adenine was alkylated with VII and XIII to give [2-(adenin-9-yl)ethoxyl]methyl(diethoxymethyl)phosphinates VIII and XIV, bearing the dialkoxymethyl protecting group on the phosphorus atom. Acid hydrolysis of compounds VIII and XIV afforded 9-(2-phosphinoethoxymethyl)adenine (X). Alkyl dialkoxymethylphosphinates V and XI reacted with paraformaldehyde to give hydroxymethylphosphinates XV and XIX which were converted into the synthons XVI, XVII and XVIII capable of introducing a protected hydroxymethylphosphino group on a hydroxy or amino group.
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KeyWords Plus:ACIDS
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ͨѶ×÷ÕßµØÖ·: ALEXANDER, P (ͨѶ×÷Õß)
ÏÔʾÔöÇ¿×éÖ¯ÐÅÏ¢µÄÃû³Æ        ACAD SCI CZECH REPUBL,INST ORGAN CHEM & BIOCHEM,CS-16610 PRAGUE 6,CZECH REPUBLIC.
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INST ORGANIC CHEM AND BIOCHEM, ACAD OF SCI CZECH REPUBLIC FLEMINGOVO NAM 2, PRAGUE 6, CZECH REPUBLIC 166 10
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Ñо¿·½Ïò:Chemistry
Web of Science Àà±ð:Chemistry, Multidisciplinary
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ÎÄÏ×ÀàÐÍ:Article
ÓïÖÖ:English
Èë²ØºÅ: WOS:A1994PG61400018
ISSN: 0010-0765
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IDS ºÅ: PG614
Web of Science ºËÐĺϼ¯ÖÐµÄ "ÒýÓõIJο¼ÎÄÏ×": 20
Web of Science ºËÐĺϼ¯ÖÐµÄ "±»ÒýƵ´Î": 6


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sunshan4379: LS-EPI+1, ¸ÐлӦÖú£¡ 2015-09-22 16:41:46
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