69471-73-4Relevant academic research and scientific papers
SYNTHESIS OF 4'-HYROXYMETHYLATED PYRIMIDINE RIBO-C-NUCLEOSIDES
Sato, T.,Noyori, R.
, p. 2535 - 2538 (2007/10/02)
A stereocontrolled synthesis of 4'-hydroxymethylated ribo-C-nucleosides and a new psico-C-nucleoside has been accomplished on the basis of the reductive cyclocoupling reaction of α,α,α',α'-tetrabromoacetone and furfuryl acetate.
REMOTE SUBSTITUENT EFFECTS IN THE BAEYER-VILLIGER OXIDATION. I. THROUGH-BOND γ SUBSTITUENT EFFECT ON THE REGIOSELECTIVITY
Noyori, R.,Sato, T.,Kobayashi, H.
, p. 2569 - 2572 (2007/10/02)
Regioselectivity of the Baeyer-Villiger oxidation of 8-oxabicyclooctan-3-one derivatives is markedly affected by the electronic nature of substituents at position γ to the carbonyl function.
