1246747-06-7Relevant academic research and scientific papers
Catalytic synthesis of enantiopure mixed diacylglycerols-synthesis of a major M. tuberculosis phospholipid and platelet activating factor
Fodran, Peter,Minnaard, Adriaan J.
, p. 6919 - 6928 (2013/10/08)
An efficient catalytic one-pot synthesis of TBDMS-protected diacylglycerols has been developed, starting from enantiopure glycidol. Subsequent migration-free deprotection leads to stereo- and regiochemically pure diacylglycerols. This novel strategy has been applied to the synthesis of a major Mycobacterium tuberculosis phospholipid, its desmethyl analogue, and platelet activating factor.
Asymmetric synthesis and structure elucidation of a glycerophospholipid from Mycobacterium tuberculosis
Ter Horst, Bjorn,Seshadri, Chetan,Sweet, Lindsay,Young, David C.,Feringa, Ben L.,Moody, D. Branch,Minnaard, Adriaan J.
scheme or table, p. 1017 - 1022 (2010/09/14)
A glycerophospholipid (1-O-tuberculostearoyl-2-O-palmitoyl-sn-glycero-3- phosphoethanolamine) from Mycobacterium tuberculosis was isolated from the reference strain H37Rv. The molecular structure of this tuberculostearoyl [(R)-10-methyloctadecyl] and palm
