Facile and chemoselective reduction of carboxylic acids to alcohols using BOP reagent and sodium borohydride
RP McGeary
Index: Tetrahedron Letters, , vol. 39, # 20 p. 3319 - 3322
Full Text: HTML
Citation Number: 64
Abstract
TETRAHEDRON LETTERS Pergamon Tetrahedron Letters 39 (1998) 3319-3322 Facile and chemoselective reduction of carboxylic acids to alcohols using BOP reagent and sodium borohydride Ross P. McGearyl ... R BOP, DIPEA NaBH4 R ~ R-CH 2-OH THF ~ 20 min, RT ...
Related Articles:
L-Aspartic acid in acyclic stereoselective synthesis. Synthetic studies on amphotericin B
[McGarvey; Williams; Hiner; et al. Journal of the American Chemical Society, 1986 , vol. 108, # 16 p. 4943 - 4952]
[Organic and Biomolecular Chemistry, , vol. 2, # 15 p. 2181 - 2187]
A facile synthesis of chiral N-protected β-amino alcohols.
[Rodriguez; Llinares; Doulut; Heitz; Martinez Tetrahedron Letters, 1991 , vol. 32, # 7 p. 923 - 926]
L-Aspartic acid in acyclic stereoselective synthesis. Synthetic studies on amphotericin B
[Journal of the American Chemical Society, , vol. 108, # 16 p. 4943 - 4952]
[Organic and Biomolecular Chemistry, , vol. 1, # 2 p. 247 - 250]