(R)-(+)-Trityl glycidyl ether
Code | Size | Price |
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TAR-T38040-1g | 1g | £128.00 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Overview
Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃
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Further Information
Bioactivity:
(R)-(+)-Trityl glycidyl ether is a precursor that has been used in the synthesis of glycerophospholipids, as well as compounds with antiviral and antimalarial activities.1,2,3
CAS:
65291-30-7
Formula:
C22H20O2
Molecular Weight:
316.4
Purity:
0.98
SMILES:
C(OC(c1ccccc1)(c1ccccc1)c1ccccc1)[C@H]1CO1
References
Hendrickson, H.S., and Hendrickson, E.K.A facile asymmetric synthesis of glycerol phospholipids via tritylglycidol prepared by the asymmetric epoxidation of allyl alcohol. Thiolester and thioether analogs of phosphatidylcholineChem. Phys. Lipids53(1)115-120(1990)
Baszczyski, O., Jansa, P., Dra??nskY, M., et al.Synthesis and antiviral activity of N9-[3-fluoro-2-(phosphonomethoxy)propyl] analogues derived from N6-substituted adenines and 2,6-diaminopurinesBioorg. Med. Chem.19(7)2114-2124(2011)
Sato, E., Morita, M., Ogawa, H., et al.Design, synthesis and anti-malarial activities of synthetic analogs of biselyngbyolide B, a Ca2+ pump inhibitor from marine cyanobacteriaBioorg. Med. Chem. Lett.28(3)298-301(2018)