Stereoselective synthesis of (25S)-25-hydroxyvitamin D3 26,23-lactone

Tetrahedron Letters

Volumn 22, Issue 27, 1981, Pages 2591-2594

  Yamada, Sachiko ^a   Nakayama, Keiko ^a   Takayama, Hiroaki ^a  

^a TEIKYO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

25 HYDROXYCOLECALCIFEROL 23,26 LACTONE; DRUG ANALYSIS; DRUG IDENTIFICATION; DRUG STRUCTURE; DRUG SYNTHESIS; IN VITRO STUDY; INFRARED SPECTROMETRY; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE; PRELIMINARY COMMUNICATION; THEORETICAL STUDY; ULTRAVIOLET SPECTROPHOTOMETRY;

EID: 0019455286     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)90528-3     Document Type: Article

References (21)

1. 25,26-Dihydroxycholecalciferol: A precursor in the renal synthesis of 25-hydroxycholecalciferol-26,23-lactone
2. Synthesis of 25-hydroxyprovitamin D3 and 25?,26-dihydroxyprovitamin D3
3. Calciferol and its relatives. Part 23. An alternative synthesis of Windaus and Grundmann's C19 ketone
4. Calciferol and its relatives. Part 23. An alternative synthesis of Windaus and Grundmann's C19 ketone
5. The influence of chain-branching on the steric outcome of some olefin-forming reactions
6. Some stereoselective and regioselective olefin additions: iodoacetoxylation and related electrophilic additions across the 22(23)-bond of 3?,5?-cycloergosta-7,22-dien-6-one
7. 655. Steroids. Part III. 11-Oxygenated steroids from 22 : 23-dibromoergosta-7 : 9(11)-dien-3?-yl acetate (ergosteryl-D acetate 22 : 23-dibromide)