89471-82-9Relevant academic research and scientific papers
STEREOSELECTIVE SYNTHESIS OF STEROID SIDE CHAIN AND CD-RINGS. A ROUTE TO (+/-)-DE-AB-CHOLESTA-8(14),22-DIEN-9-ONE.
Takahashi, Takashi,Ueno, Hiroaki,Miyazawa, Masahiro,Tsuji, Jiro
, p. 4463 - 4466 (2007/10/02)
The stereoselective synthesis of (+/-)-de-AB-cholesta-8(14),22-dien-9-one from (+/-)-erythro-6-benzyloxy-5-hydroxy-8-methyl-1-tetrahydropyranyloxy-3(Z)-nonene by two Claisen rearrangements as a precursor of vitamin D3 is presented.
STEREOSELECTIVE REDUCTION OF α-ALKOXY ACETYLENIC KETONES WITH ZINC BOROHYDRIDE AND K-SELECTRIDE.
Takashi, Takahashi,Masahiro, Miyazawa,Jiro, Tsuji
, p. 5139 - 5142 (2007/10/02)
Reduction of α-benzyloxy acetylenic ketones with zinc borohydride afforded the erythro-acetylenic vicinal diols in 95percent stereoselectivity, while reduction with K-selectride gave the isomeric threo-diols in 90percent stereoselectivity.
