Synthesis of all possible A-ring diastereomers at the 1- and 3-positions of 1α,25-dihydroxy-2β-(3-hydroxypropoxy)vitamin D3 (ED-71) using C2-symmetrical epoxide as a common starting material

Anticancer Research

Volumn 29, Issue 9, 2009, Pages 3571-3578

  Kubodera, Noboru ^a   Hatakeyama, Susumi ^b  

^a CHUGAI PHARMACEUTICAL CO LTD   (Japan)

^b NAGASAKI UNIVERSITY   (Japan)

Author keywords

1 ,25 Dihydroxyvitamin D3; 1 25 dihydroxy 2 (3 hydroxypropoxy)vitamin D3; 1,3 diepi ED 71; 1 epi ED 71; 3 epi ED 71; ED 71

Indexed keywords

2BETA (3 HYDROXYPROPOXY)CALCITRIOL; EPOXIDE;

CONFERENCE PAPER; CONTROLLED STUDY; DIASTEREOISOMER; DRUG ACTIVITY; DRUG STRUCTURE; DRUG SYNTHESIS; PRIORITY JOURNAL; STRUCTURE ACTIVITY RELATION;

CALCITRIOL; EPOXY COMPOUNDS; MAGNETIC RESONANCE SPECTROSCOPY; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION; SPECTROPHOTOMETRY, ULTRAVIOLET; STEREOISOMERISM;

EID: 68549097953     PISSN: 02507005     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

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