Enantiospecific synthesis of some bioactive amino alcohols and related compounds from cyclohexylideneglyceraldehyde
A Sharma, S Chattopadhyay
Index: Sharma, Anubha; Chattopadhyay, Subrata Tetrahedron Asymmetry, 1999 , vol. 10, # 5 p. 883 - 890
Full Text: HTML
Citation Number: 14
Abstract
Two bioactive amino alcohols or related derivatives, 2-aminohexadecanol I and erythro-9-(2- hydroxy-3-nonyl) adenine hydrochloride (EHNA hydrochloride) IIa, have been synthesized from some enantiomerically pure 3-alkylglycerols. The required C-3 epimeric 3- alkylglycerols were, in turn, prepared by simple Grignard addition to cyclohexylideneglyceraldehyde 1 followed by column chromatography.
Related Articles:
[Baker, David C.; Hawkins, L. D. Journal of Organic Chemistry, 1982 , vol. 47, # 11 p. 2179 - 2184]
[Baker, David C.; Hawkins, L. D. Journal of Organic Chemistry, 1982 , vol. 47, # 11 p. 2179 - 2184]
[Baker, David C.; Hawkins, L. D. Journal of Organic Chemistry, 1982 , vol. 47, # 11 p. 2179 - 2184]
[Baker, David C.; Hawkins, L. D. Journal of Organic Chemistry, 1982 , vol. 47, # 11 p. 2179 - 2184]