• 8.5 g (40 mmol) 1-(3-indolyl)-2-nitrobutene was added during 30 minutes to a solution of 1.9 g (50 mmol, 1,25 mol eq.) sodium borohydride in 25 ml water and 50 ml IPA. (thevespiary.org)
  • Stoichiometric reducing agents to accomplish this task include lithium aluminium hydride, sodium borohydride, alkoxy borohydrides, alkoxy aluminium hydrides, and boranes. (wikipedia.org)
  • carbonation of the vicinal hydroxyls at the 1- and 14-position with phosgene in mehtylene chloride/toluene mixture in the presence of pyridine to give the 1, 14-carbonate derivative: reduction of the carbonyl at the 13-position with sodium borohydride in methanol: removal of the protective groups at the 7- and 10-position to give 14ß-hydroxy-l,14-carbonate-deacetylbaccatin III. (allindianpatents.com)
  • 8.5 g (40 mmol) 1-(3-indolyl)-2-nitrobutene was added during 30 minutes to a solution of 1.9 g (50 mmol, 1,25 mol eq.) sodium borohydride in 25 ml water and 50 ml IPA. (thevespiary.org)
  • Stoichiometric reducing agents to accomplish this task include lithium aluminium hydride, sodium borohydride, alkoxy borohydrides, alkoxy aluminium hydrides, and boranes. (wikipedia.org)
  • A tert-butyl (R)-(1-benzylpyrrolidin-3-yl)carbamate 2aa (3.20g, 11.6mmol) solution in 58.0mL of 61 tetrahydrofuran was placed in a 100mL round-bottom flask. (ambeed.com)