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Volumn 45, Issue 43, 2004, Pages 8003-8006

Nucleophilic transformations of cyclic phosphate triesters

Author keywords

Cyclic phosphate triesters; Grignard reagents; Nucleophilic attacks; Phosphites; Phosphonates

Indexed keywords

2 ETHOXY 1,3,2 DIOXAPHOSPHOLANE 2 OXIDE; 2 ETHOXY 1,3,2 DIOXAPHOSPHORINANE 2 OXIDE; CARBON; ESTER DERIVATIVE; ETHYL 2 HYDROXYETHYLPHOSPHITE; HALIDE; MAGNESIUM DERIVATIVE; PHOSPHATE; PHOSPHITE; PHOSPHONIC ACID DERIVATIVE; PHOSPHORUS DERIVATIVE; SODIUM BOROHYDRIDE; SODIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 4644351843     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.09.011     Document Type: Article
Times cited : (16)

References (49)
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    • Ref. 9
    • Ref. 9
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    • note
    • 2O-MeOH (20:1)
  • 37
    • 84982450804 scopus 로고
    • This compound was also obtained, in similar yields, from the corresponding N-pyrazolyl phenyl phosphonoamidate and ethylene glycol, see: U. Felcht, and M. Regitz Chem. Ber. 109 1976 3675
    • (1976) Chem. Ber. , vol.109 , pp. 3675
    • Felcht, U.1    Regitz, M.2
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    • note
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  • 48
    • 4644238611 scopus 로고    scopus 로고
    • note
    • 4, filtered and the solvent was evaporated under vacuum. The crude oily product was charged on a silica gel column and was eluted with hexane:ethyl acetate (3:1) to afford 3 as a colorless oil (0.334 g, 2.2 mmol, 66% yield)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.