| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-83 |
Sentence |
denotes |
Cyclic platelet-activating factor analogues derived from 2-deoxy-D-erythro-pentose. |
| TextSentencer_T2 |
84-186 |
Sentence |
denotes |
A method for the synthesis of chiral cyclic analogues of platelet-activating factor (PAF) is reported. |
| TextSentencer_T3 |
187-375 |
Sentence |
denotes |
Treatment of suitably substituted derivatives of 2-deoxy-D-erythro-pentose with phosphorus oxychloride, followed by choline p-toluenesulfonate generates cyclic phospholipids in good yield. |
| TextSentencer_T4 |
376-633 |
Sentence |
denotes |
Further chemical modification produces other compounds including optically active gamma-butyrolactones such as 2-deoxy-5-O-hexadecyl-3-O-phosphocholyl-D-erythro-pentono-1, 4-lactone and 2-deoxy-3-O-hexadecyl-5-O-phosphocholyl-D-erythro-pentono-1, 4-lactone. |
| TextSentencer_T5 |
634-756 |
Sentence |
denotes |
All phospholipids were poor antagonists of PAF-induced aggregation of human platelets, and two analogs were poor agonists. |
| TextSentencer_T6 |
757-870 |
Sentence |
denotes |
The chemistry presented should be useful for the syntheses of other conformationally restricted analogues of PAF. |
| T1 |
0-83 |
Sentence |
denotes |
Cyclic platelet-activating factor analogues derived from 2-deoxy-D-erythro-pentose. |
| T2 |
84-186 |
Sentence |
denotes |
A method for the synthesis of chiral cyclic analogues of platelet-activating factor (PAF) is reported. |
| T3 |
187-375 |
Sentence |
denotes |
Treatment of suitably substituted derivatives of 2-deoxy-D-erythro-pentose with phosphorus oxychloride, followed by choline p-toluenesulfonate generates cyclic phospholipids in good yield. |
| T4 |
376-633 |
Sentence |
denotes |
Further chemical modification produces other compounds including optically active gamma-butyrolactones such as 2-deoxy-5-O-hexadecyl-3-O-phosphocholyl-D-erythro-pentono-1, 4-lactone and 2-deoxy-3-O-hexadecyl-5-O-phosphocholyl-D-erythro-pentono-1, 4-lactone. |
| T5 |
634-756 |
Sentence |
denotes |
All phospholipids were poor antagonists of PAF-induced aggregation of human platelets, and two analogs were poor agonists. |
| T6 |
757-870 |
Sentence |
denotes |
The chemistry presented should be useful for the syntheses of other conformationally restricted analogues of PAF. |