60031-91-6Relevant articles and documents
Total Syntheses of Naucleamides A-C and E, Geissoschizine, Geissoschizol, (E)-Isositsirikine, and 16-epi-(E)-Isositsirikine
Li, Lei,Aibibula, Paruke,Jia, Qianlan,Jia, Yanxing
, p. 2642 - 2645 (2017/05/24)
A divergent approach for the enantioselective total synthesis of eight monoterpenoid indole alkaloids was developed. The approach allows the first total syntheses of naucleamides A-C and E in only 6-8 steps and also enables the efficient synthesis of geissoschizine, geissoschizol, (E)-isositsirikine, and 16-epi-(E)-isositsirikine in 10-11 steps from commercially available crotonic aldehyde. The synthesis features a one-pot organocatalyzed asymmetric Michael addition/Pictet-Spengler reaction. Notably, biomimetic synthesis of naucleamide E was achieved by oxidative cyclization of naucleamide A.
ALKALOIDS FROM RHAZYA STRICTA
Atta-Ur-Rahman,Zaman, Khurshid,Perveen, Shahnaz,Habib-Ur-Rehman,Muzaffar, Anjum,et al.
, p. 1285 - 1294 (2007/10/02)
Chemical investigations of roots and leaves of Rhazya stricta have resulted in the isolation of the new indole alkaloids, 16R-19,20-E-isositsirikine acetate, leepacine and dihydroeburnamenine, along with six known alkaloids.Among these, (-)-16R,21R-O-methyleburnamine, 2-ethyl-3-indole, (20S)-19,20-dihydrocondylocarpine and N-acetylaspidospermidine have been isolated for the first time from R. stricta.Spectral studies on (+)-21S-eburnamenine and the glycoalkaloid strictosamide have also been undertaken. --- Key Word Index: Rhazya stricta; Apocynaceae; indole alkaloide; glycoalkaloids; 13C NMR.
Preparation and H(3) Isomerization of C(15)-Substituted Deplancheine Derivatives. Synthesis of Geissoschizol and Geissoschizine
Wenkert, Ernest,Guo, Ming,Pestchanker, Mauricio J.,Shi, Yao-Jun,Vankar, Yashwant D.
, p. 1166 - 1174 (2007/10/02)
A series of indoloquinolizidines have been prepared by the two-step scheme of nucleophile addition to 1-tryptophyl-3-acylpyridinium salts or their vinylogues and subsequent, acid-catalyzed cyclization.Acid-induced hydrolysis, decarboxylation, and reduction of the resultant vinylogous urethanes has opened an approach to antirhine and yielded C(15)-substituted deplancheine derivatives.Functional group manipulation of the latter has permitted the syntheses of geissoschizol and geissoschizine.