Conclusions
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1.
A new total synthesis of R-α-L-alanyl-γ-L-phosphatidylglycerin, optically active at all the asymmetric centers, was carried out.
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2.
A comparison of the synthetic preparation with the lipoamino acid fromClostridium welchii indicates that the latter is S-1-(L-phosphatidyl)-3-alanylglycerin.
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Literature cited
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 925–927, April, 1967.
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Molotkovskii, Y.G., Bergel'son, L.D. Synthesis of the R-form of α-phosphatidyl-α-alanylglycerin and investigation of the configuration of bacterial lipoamino acids. Russ Chem Bull 16, 893–894 (1967). https://doi.org/10.1007/BF00915683
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DOI: https://doi.org/10.1007/BF00915683