223 related articles for article (PubMed ID: 18081287)
1. Strictosidine synthase: mechanism of a Pictet-Spengler catalyzing enzyme.
Maresh JJ; Giddings LA; Friedrich A; Loris EA; Panjikar S; Trout BL; Stöckigt J; Peters B; O'Connor SE
J Am Chem Soc; 2008 Jan; 130(2):710-23. PubMed ID: 18081287
[TBL] [Abstract][Full Text] [Related]
2. Asymmetric Synthesis of (R)-1-Alkyl-Substituted Tetrahydro-ß-carbolines Catalyzed by Strictosidine Synthases.
Pressnitz D; Fischereder EM; Pletz J; Kofler C; Hammerer L; Hiebler K; Lechner H; Richter N; Eger E; Kroutil W
Angew Chem Int Ed Engl; 2018 Aug; 57(33):10683-10687. PubMed ID: 29852524
[TBL] [Abstract][Full Text] [Related]
3. Exploring the Chemistry of Spiroindolenines by Mechanistically-Driven Reaction Development: Asymmetric Pictet-Spengler-type Reactions and Beyond.
Zheng C; You SL
Acc Chem Res; 2020 Apr; 53(4):974-987. PubMed ID: 32275392
[TBL] [Abstract][Full Text] [Related]
4. Inverted Binding of Non-natural Substrates in Strictosidine Synthase Leads to a Switch of Stereochemical Outcome in Enzyme-Catalyzed Pictet-Spengler Reactions.
Eger E; Simon A; Sharma M; Yang S; Breukelaar WB; Grogan G; Houk KN; Kroutil W
J Am Chem Soc; 2020 Jan; 142(2):792-800. PubMed ID: 31909617
[TBL] [Abstract][Full Text] [Related]
5. Structural Basis for β-Carboline Alkaloid Production by the Microbial Homodimeric Enzyme McbB.
Mori T; Hoshino S; Sahashi S; Wakimoto T; Matsui T; Morita H; Abe I
Chem Biol; 2015 Jul; 22(7):898-906. PubMed ID: 26120001
[TBL] [Abstract][Full Text] [Related]
6. Strictosidine synthase, an indispensable enzyme involved in the biosynthesis of terpenoid indole and β-carboline alkaloids.
Cao N; Wang CH
Chin J Nat Med; 2021 Aug; 19(8):591-607. PubMed ID: 34419259
[TBL] [Abstract][Full Text] [Related]
7. Organocatalytic Enantioselective Pictet-Spengler Reaction of α-Ketoesters: Development and Application to the Total Synthesis of (+)-Alstratine A.
Andres R; Sun F; Wang Q; Zhu J
Angew Chem Int Ed Engl; 2023 Jan; 62(1):e202213831. PubMed ID: 36347809
[TBL] [Abstract][Full Text] [Related]
8. Substrate specificity of strictosidine synthase.
McCoy E; Galan MC; O'Connor SE
Bioorg Med Chem Lett; 2006 May; 16(9):2475-8. PubMed ID: 16481164
[TBL] [Abstract][Full Text] [Related]
9. Increasing the Diversity of Known Pictet-Spenglerases.
Tanner ME
Chem Biol; 2015 Jul; 22(7):806-7. PubMed ID: 26207293
[TBL] [Abstract][Full Text] [Related]
10. β-Methyltryptamine Provoking the Crucial Role of Strictosidine Synthase Tyr151-OH for Its Stereoselective Pictet-Spengler Reactions to Tryptoline-type Alkaloids.
Liu H; Panjikar S; Sheng X; Futamura Y; Zhang C; Shao N; Osada H; Zou H
ACS Chem Biol; 2022 Jan; 17(1):187-197. PubMed ID: 34994203
[TBL] [Abstract][Full Text] [Related]
11. Discovery of McbB, an enzyme catalyzing the β-carboline skeleton construction in the marinacarboline biosynthetic pathway.
Chen Q; Ji C; Song Y; Huang H; Ma J; Tian X; Ju J
Angew Chem Int Ed Engl; 2013 Sep; 52(38):9980-4. PubMed ID: 23913777
[TBL] [Abstract][Full Text] [Related]
12. Catalytic Enantioselective Pictet-Spengler Reaction of α-Ketoamides Catalyzed by a Single H-Bond Donor Organocatalyst.
Andres R; Wang Q; Zhu J
Angew Chem Int Ed Engl; 2022 May; 61(19):e202201788. PubMed ID: 35225416
[TBL] [Abstract][Full Text] [Related]
13. Asymmetric Biocatalytic Synthesis of 1-Aryltetrahydro-β-carbolines Enabled by "Substrate Walking".
Eger E; Schrittwieser JH; Wetzl D; Iding H; Kuhn B; Kroutil W
Chemistry; 2020 Dec; 26(69):16281-16285. PubMed ID: 33017078
[TBL] [Abstract][Full Text] [Related]
14. 3D-Structure and function of strictosidine synthase--the key enzyme of monoterpenoid indole alkaloid biosynthesis.
Stöckigt J; Barleben L; Panjikar S; Loris EA
Plant Physiol Biochem; 2008 Mar; 46(3):340-55. PubMed ID: 18280746
[TBL] [Abstract][Full Text] [Related]
15. Catalytic asymmetric Pictet-Spengler reaction.
Seayad J; Seayad AM; List B
J Am Chem Soc; 2006 Feb; 128(4):1086-7. PubMed ID: 16433519
[TBL] [Abstract][Full Text] [Related]
16. Characterization of a new microbial Pictet-Spenglerase NscbB affording the β-carboline skeletons from Nocardiopsis synnemataformans DSM 44143.
Chen Q; Zhang S; Xie Y
J Biotechnol; 2018 Sep; 281():137-143. PubMed ID: 29981450
[TBL] [Abstract][Full Text] [Related]
17. Total Syntheses of (-)-Strictosidine and Related Indole Alkaloid Glycosides.
Sakamoto J; Umeda Y; Rakumitsu K; Sumimoto M; Ishikawa H
Angew Chem Int Ed Engl; 2020 Aug; 59(32):13414-13422. PubMed ID: 32364625
[TBL] [Abstract][Full Text] [Related]
18. Mechanistic studies on the cis to trans epimerization of trisubstituted 1,2,3,4-tetrahydro-beta-carbolines.
Van Linn ML; Cook JM
J Org Chem; 2010 Jun; 75(11):3587-99. PubMed ID: 20429580
[TBL] [Abstract][Full Text] [Related]
19. Total synthesis of (+)-yohimbine via an enantioselective organocatalytic Pictet-Spengler reaction.
Herlé B; Wanner MJ; van Maarseveen JH; Hiemstra H
J Org Chem; 2011 Nov; 76(21):8907-12. PubMed ID: 21950549
[TBL] [Abstract][Full Text] [Related]
20. Development of the Pictet-Spengler reaction catalyzed by AuCl3/AgOTf.
Youn SW
J Org Chem; 2006 Mar; 71(6):2521-3. PubMed ID: 16526809
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
