SYNTHESIS AND STRUCTURAL-ANALYSIS OF STEREOSPECIFIC 3,4,5-TRISUBSTITUTED GAMMA-BUTYROLACTONE PHOSPHOLIPIDS

被引:0
|
作者
LI, X [1 ]
ROTELLA, DP [1 ]
机构
[1] UNIV MISSISSIPPI,SCH PHARM,DEPT PHARMACOGNOSY,UNIVERSITY,MS 38677
关键词
D O I
10.1007/BF02536731
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The first synthesis of stereospecific 3,4,5-trisubstituted gamma-butyrolactone phospholipids has been achieved by a ten-step sequence starting from N,N-dimethylacetamide (9). Alkylation of 9 with 1-bromohexane gave N,N-dimethyloctanamide (11), which was subjected to aldol condensation with acrolein and afforded the erythro-N,N-dimethyl-3-hydroxy-2-hexyl-4-pentena (6) and its threo isomer 7, both of which were subsequently converted to the corresponding 3-oxy(hexanoyl) esters 15 and 16. Stereospecific cyclization of diastereomeric allylic amides (6,7,15 and 16) via iodolactonization gave 3,4,5-trisubstituted gamma-butyrolactones (19-25) in satisfactory yields (68-89%) and with high stereoselectivity (at least 6:1), except for the three amide 16 (2:1). Conversion of the 6-iodo-group of the major iodolactones 23 and 24 to the corresponding 6-hydroxy lactones 31 and 32 through a wet Prevost reaction also resulted in 4-hydroxy droxy lactones 30 and 33, and a mechanism for this reaction is proposed. Further phosphorylation of 4- or 6-hydroxy lactones 30, 31 and 32 with diphenyl chlorophosphate gave the corresponding diphenyl phosphoric acid lactone esters 34, 35 and 36, whereas 33 underwent an elimination reaction under formation of a C(3)-C(4) double bond. Hydrogenolysis of the diphenyl groups of esters 34, 35 and 36 over Adams' catalyst [platinum(IV) oxide] yielded the corresponding phosphoric acid lactone esters 38, 39 and 40, which were finally treated with choline tetraphenylborate to afford the desired lactone phospholipids 41, 42 and 43 in overall yields of 9, 30 and 18%, respectively. The structures of all new compounds were unambiguously assigned by analysis of their H-1 and C-13 one dimensional and two-dimensional nuclear magnetic resonance (NMR) spectra obtained on a 300 MHz NMR spectrometer, and the structures were confirmed by low or high resolution mass spectrometry as well as elemental analysis. The stereoisomeric purity of the final products (98.2, 99.0 and 98.5% for 41, 42 and 43, respectively) was determined by high-performance liquid chromatography.
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页码:211 / 224
页数:14
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