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N-acyldihydropyridones as synthetic intermediates. synthesis of (±)-septicine and (±)-tylophorine.

✍ Scribed by Daniel L. Comins; Lawrence A. Morgan


Publisher
Elsevier Science
Year
1991
Tongue
French
Weight
247 KB
Volume
32
Category
Article
ISSN
0040-4039

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✦ Synopsis


The mdohzrdme alkalords (+)-septlane and (k)-tylophonne were prepared from N-acyldLhydropyndone 7 tn five and SW steps, respectively

Recently we hdve been studying the synthesis and synthetic utility of N-acyl-2,3-dlhydm-4-pyndoneq These highly functlonJlzed heterocycles are conveniently prepared by the addition of Gngnard reagents to 1-acyl-4-methoxypyndlnlun~ s&s ' Previously, plpendme2, qumol~zldme'~3, and crs-decahydroqulnohne4


📜 SIMILAR VOLUMES


Enantiopure N-acyldihydropyridones as sy
✍ Daniel L. Comins; Nezha Radi Benjelloun 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 259 KB

The trans-pip&dine alkaloid, (-)-solenopsin A. was prepared in seven steps from readily available 4-~haxy-3\_(niiropropyrsilyllpyrfdin in 43% overall yield. The addition of organ~tallics to chiral 1-acylpyridinium salt 1 gives N-acyl-2-alkyl-23&hydta~4pyridones 2 with high diastereoselectivity.\*~ T