Synthesis of the enantiomer of 1α,25-dihydroxy vitamin D3 (calcitriol) and a diastereomer of 1α,25-dihydroxy vitamin D3 differing from natural product in configuration at all but one asymmetric carbon atoms

Polish Journal of Chemistry

Volumn 79, Issue 2, 2005, Pages 413-428

  Achmatowicz, B ^a   Przezdziecka, A ^a   Wicha, J ^a  

^a INSTITUTE OF ORGANIC CHEMISTRY   (Poland)

Author keywords

Convergent synthesis; Mitsunobu reaction; Olefination reaction; Vitamins D

Indexed keywords

CALCITRIOL; CARBON; HYDROXYL GROUP; NATURAL PRODUCT; SILANE DERIVATIVE;

ARTICLE; BENZYLATION; DEPROTECTION REACTION; DIASTEREOISOMER; DIHYDROXYLATION; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; OLEFINATION; STEREOCHEMISTRY;

EID: 14144253798     PISSN: 01375083     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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