180 related articles for article (PubMed ID: 20392128)
1. Enantiospecific total synthesis of the important biogenetic intermediates along the ajmaline pathway, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epivellosimine and macusine A.
Yin W; Kabir MS; Wang Z; Rallapalli SK; Ma J; Cook JM
J Org Chem; 2010 May; 75(10):3339-49. PubMed ID: 20392128
[TBL] [Abstract][Full Text] [Related]
2. First enantiospecific total synthesis of the important biogenetic intermediates, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epi-vellosimine and macusine A.
Yin W; Ma J; Rivas FM; Cook JM
Org Lett; 2007 Jan; 9(2):295-8. PubMed ID: 17217288
[TBL] [Abstract][Full Text] [Related]
3. General approach for the synthesis of 12-methoxy-substituted sarpagine indole alkaloids including (-)-12-methoxy-N(b)-methylvoachalotine, (+)-12-methoxy-N(a)-methylvellosimine, (+)-12-methoxyaffinisine, and (-)-fuchsiaefoline.
Zhou H; Liao X; Yin W; Ma J; Cook JM
J Org Chem; 2006 Jan; 71(1):251-9. PubMed ID: 16388644
[TBL] [Abstract][Full Text] [Related]
4. A general strategy for the synthesis of vincamajine-related indole alkaloids: stereocontrolled total synthesis of (+)-dehydrovoachalotine, (-)-vincamajinine, and (-)-11-methoxy-17-epivincamajine as well as the related quebrachidine diol, vincamajine diol, and vincarinol.
Yu J; Wearing XZ; Cook JM
J Org Chem; 2005 May; 70(10):3963-79. PubMed ID: 15876085
[TBL] [Abstract][Full Text] [Related]
5. General approach for the synthesis of sarpagine indole alkaloids. Enantiospecific total synthesis of (+)-vellosimine, (+)-normacusine B, (-)-alkaloid Q3, (-)-panarine, (+)-Na-methylvellosimine, and (+)-Na-methyl-16-epipericyclivine.
Yu J; Wang T; Liu X; Deschamps J; Flippen-Anderson J; Liao X; Cook JM
J Org Chem; 2003 Oct; 68(20):7565-81. PubMed ID: 14510528
[TBL] [Abstract][Full Text] [Related]
6. General approach for the synthesis of sarpagine/ajmaline indole alkaloids. Stereospecific total synthesis of the sarpagine alkaloid (+)-vellosimine.
Wang T; Cook JM
Org Lett; 2000 Jul; 2(14):2057-9. PubMed ID: 10891229
[TBL] [Abstract][Full Text] [Related]
7. Characterization of polyneuridine aldehyde esterase, a key enzyme in the biosynthesis of sarpagine/ajmaline type alkaloids.
Pfitzner A; Stöckigt J
Planta Med; 1983 Aug; 48(8):221-7. PubMed ID: 17404987
[TBL] [Abstract][Full Text] [Related]
8. The enantiospecific, stereospecific total synthesis of the ring-A oxygenated sarpagine indole alkaloids (+)-majvinine, (+)-10-methoxyaffinisine, and (+)-N(a)-methylsarpagine, as well as the total synthesis of the alstonia bisindole alkaloid macralstonidine.
Zhao S; Liao X; Wang T; Flippen-Anderson J; Cook JM
J Org Chem; 2003 Aug; 68(16):6279-95. PubMed ID: 12895062
[TBL] [Abstract][Full Text] [Related]
9. Enantiospecific total synthesis of (-)-(E)16-epiaffinisine, (+)-(E)16-epinormacusine B, and (+)-dehydro-16-epiaffinisine as well as the stereocontrolled total synthesis of alkaloid G.
Yu J; Wang T; Wearing XZ; Ma J; Cook JM
J Org Chem; 2003 Jul; 68(15):5852-9. PubMed ID: 12868917
[TBL] [Abstract][Full Text] [Related]
10. Total Synthesis of Sarpagine-Related Bioactive Indole Alkaloids.
Rahman MT; Deschamps JR; Imler GH; Cook JM
Chemistry; 2018 Feb; 24(10):2354-2359. PubMed ID: 29244896
[TBL] [Abstract][Full Text] [Related]
11. Stereocontrolled total synthesis of (-)-vincamajinine and (-)-11-methoxy-17-epivincamajine.
Yu J; Wearing XZ; Cook JM
J Am Chem Soc; 2004 Feb; 126(5):1358-9. PubMed ID: 14759191
[TBL] [Abstract][Full Text] [Related]
12. General approach for the synthesis of sarpagine/macroline indole alkaloids. Enantiospecific total synthesis of the indole alkaloid trinervine.
Liu X; Cook JM
Org Lett; 2001 Dec; 3(25):4023-6. PubMed ID: 11735575
[TBL] [Abstract][Full Text] [Related]
13. Regiospecific, enantiospecific total synthesis of the 12-alkoxy-substituted indole alkaloids, (+)-12-methoxy-Na-methylvellosimine, (+)-12-methoxyaffinisine, and (-)-fuchsiaefoline.
Zhou H; Liao X; Cook JM
Org Lett; 2004 Jan; 6(2):249-52. PubMed ID: 14723540
[TBL] [Abstract][Full Text] [Related]
14. Enantiospecific total synthesis of the sarpagine related indole alkaloids talpinine and talcarpine as well as the improved total synthesis of alstonerine and anhydromacrosalhine-methine via the asymmetric Pictet-Spengler reaction.
Yu P; Wang T; Li J; Cook JM
J Org Chem; 2000 May; 65(10):3173-91. PubMed ID: 10814213
[TBL] [Abstract][Full Text] [Related]
15. Stereospecific approach to the synthesis of ring-A oxygenated sarpagine indole alkaloids. Total synthesis of the dimeric indole alkaloid P-(+)-dispegatrine and six other monomeric indole alkaloids.
Edwankar CR; Edwankar RV; Namjoshi OA; Liao X; Cook JM
J Org Chem; 2013 Jul; 78(13):6471-87. PubMed ID: 23721107
[TBL] [Abstract][Full Text] [Related]
16. Enantioselective total synthesis of desbromoarborescidines A-C and the formal synthesis of (S)-deplancheine.
Mondal P; Argade NP
J Org Chem; 2013 Jul; 78(13):6802-8. PubMed ID: 23758537
[TBL] [Abstract][Full Text] [Related]
17. Potential active-site residues in polyneuridine aldehyde esterase, a central enzyme of indole alkaloid biosynthesis, by modelling and site-directed mutagenesis.
Mattern-Dogru E; Ma X; Hartmann J; Decker H; Stöckigt J
Eur J Biochem; 2002 Jun; 269(12):2889-96. PubMed ID: 12071952
[TBL] [Abstract][Full Text] [Related]
18. An improved total synthesis of (+)-macroline and alstonerine as well as the formal total synthesis of (-)-talcarpine and (-)-anhydromacrosalhine-methine.
Liao X; Zhou H; Yu J; Cook JM
J Org Chem; 2006 Nov; 71(23):8884-90. PubMed ID: 17081019
[TBL] [Abstract][Full Text] [Related]
19. Structure units oriented approach towards collective synthesis of sarpagine-ajmaline-koumine type alkaloids.
Chen W; Ma Y; He W; Wu Y; Huang Y; Zhang Y; Tian H; Wei K; Yang X; Zhang H
Nat Commun; 2022 Feb; 13(1):908. PubMed ID: 35177620
[TBL] [Abstract][Full Text] [Related]
20. Concise total synthesis of (+/-)-pseudotabersonine via double ring-closing metathesis strategy.
Cheng B; Sunderhaus JD; Martin SF
Org Lett; 2010 Aug; 12(16):3622-5. PubMed ID: 20704405
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]