157 related articles for article (PubMed ID: 29345260)
1. One-pot chemoenzymatic synthesis of trolline and tetrahydroisoquinoline analogues.
Zhao J; Lichman BR; Ward JM; Hailes HC
Chem Commun (Camb); 2018 Feb; 54(11):1323-1326. PubMed ID: 29345260
[TBL] [Abstract][Full Text] [Related]
2. Engineering a norcoclaurine synthase for one-step synthesis of (S)-1-aryl-tetrahydroisoquinolines.
Zhang M; Huang ZY; Su Y; Chen FF; Chen Q; Xu JH; Zheng GW
Bioresour Bioprocess; 2023 Mar; 10(1):15. PubMed ID: 38647611
[TBL] [Abstract][Full Text] [Related]
3. Occurrence of Enantioselectivity in Nature: The Case of (S)-Norcoclaurine.
Ghirga F; Quaglio D; Ghirga P; Berardozzi S; Zappia G; Botta B; Mori M; D'Acquarica I
Chirality; 2016 Mar; 28(3):169-80. PubMed ID: 26729048
[TBL] [Abstract][Full Text] [Related]
4. A Catalytic Asymmetric Pictet-Spengler Platform as a Biomimetic Diversification Strategy toward Naturally Occurring Alkaloids.
Scharf MJ; List B
J Am Chem Soc; 2022 Aug; 144(34):15451-15456. PubMed ID: 35976162
[TBL] [Abstract][Full Text] [Related]
5. Chemoenzymatic Cascades toward Methylated Tetrahydroprotoberberine and Protoberberine Alkaloids.
Roddan R; Subrizi F; Broomfield J; Ward JM; Keep NH; Hailes HC
Org Lett; 2021 Aug; 23(16):6342-6347. PubMed ID: 34355910
[TBL] [Abstract][Full Text] [Related]
6. [Research progress of Pictet-Spenglerases].
Xie Y; Chen Q; Zhang S; Shen C
Sheng Wu Gong Cheng Xue Bao; 2020 Oct; 36(10):2001-2016. PubMed ID: 33169566
[TBL] [Abstract][Full Text] [Related]
7. Single step syntheses of (1S)-aryl-tetrahydroisoquinolines by norcoclaurine synthases.
Roddan R; Sula A; Méndez-Sánchez D; Subrizi F; Lichman BR; Broomfield J; Richter M; Andexer JN; Ward JM; Keep NH; Hailes HC
Commun Chem; 2020 Nov; 3(1):170. PubMed ID: 36703392
[TBL] [Abstract][Full Text] [Related]
8. One-pot Ugi-azide and Heck reactions for the synthesis of heterocyclic systems containing tetrazole and 1,2,3,4-tetrahydroisoquinoline.
Niu J; Wang Y; Yan S; Zhang Y; Ma X; Zhang Q; Zhang W
Beilstein J Org Chem; 2024; 20():912-920. PubMed ID: 38711586
[TBL] [Abstract][Full Text] [Related]
9. Asymmetric synthesis of tetrahydroisoquinolines by enzymatic Pictet-Spengler reaction.
Nishihachijo M; Hirai Y; Kawano S; Nishiyama A; Minami H; Katayama T; Yasohara Y; Sato F; Kumagai H
Biosci Biotechnol Biochem; 2014; 78(4):701-7. PubMed ID: 25036970
[TBL] [Abstract][Full Text] [Related]
10. Enzymatic and Chemoenzymatic Three-Step Cascades for the Synthesis of Stereochemically Complementary Trisubstituted Tetrahydroisoquinolines.
Erdmann V; Lichman BR; Zhao J; Simon RC; Kroutil W; Ward JM; Hailes HC; Rother D
Angew Chem Int Ed Engl; 2017 Oct; 56(41):12503-12507. PubMed ID: 28727894
[TBL] [Abstract][Full Text] [Related]
11. Biomimetic Phosphate-Catalyzed Pictet-Spengler Reaction for the Synthesis of 1,1'-Disubstituted and Spiro-Tetrahydroisoquinoline Alkaloids.
Zhao J; Méndez-Sánchez D; Ward JM; Hailes HC
J Org Chem; 2019 Jun; 84(12):7702-7710. PubMed ID: 31095375
[TBL] [Abstract][Full Text] [Related]
12. Stereoselective Three-Step One-Pot Cascade Combining Amino- and Biocatalysis to Access Chiral γ-Nitro Alcohols.
Ascaso-Alegre C; Herrera RP; Mangas-Sánchez J
Angew Chem Int Ed Engl; 2022 Oct; 61(40):e202209159. PubMed ID: 35983936
[TBL] [Abstract][Full Text] [Related]
13. Manganese dioxide mediated one-pot synthesis of methyl 9H-pyrido[3,4-b]indole-1-carboxylate: Concise synthesis of alangiobussinine.
Baiget J; Llona-Minguez S; Lang S; Mackay SP; Suckling CJ; Sutcliffe OB
Beilstein J Org Chem; 2011; 7():1407-11. PubMed ID: 22043251
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Scaffold tailoring by a newly detected Pictet-Spenglerase activity of strictosidine synthase: from the common tryptoline skeleton to the rare piperazino-indole framework.
Wu F; Zhu H; Sun L; Rajendran C; Wang M; Ren X; Panjikar S; Cherkasov A; Zou H; Stöckigt J
J Am Chem Soc; 2012 Jan; 134(3):1498-500. PubMed ID: 22229634
[TBL] [Abstract][Full Text] [Related]
16. Multienzyme One-Pot Cascades Incorporating Methyltransferases for the Strategic Diversification of Tetrahydroisoquinoline Alkaloids.
Subrizi F; Wang Y; Thair B; Méndez-Sánchez D; Roddan R; Cárdenas-Fernández M; Siegrist J; Richter M; Andexer JN; Ward JM; Hailes HC
Angew Chem Int Ed Engl; 2021 Aug; 60(34):18673-18679. PubMed ID: 34101966
[TBL] [Abstract][Full Text] [Related]
17. Multienzyme One-Pot Cascades Incorporating Methyltransferases for the Strategic Diversification of Tetrahydroisoquinoline Alkaloids.
Subrizi F; Wang Y; Thair B; Méndez-Sánchez D; Roddan R; Cárdenas-Fernández M; Siegrist J; Richter M; Andexer JN; Ward JM; Hailes HC
Angew Chem Weinheim Bergstr Ger; 2021 Aug; 133(34):18821-18827. PubMed ID: 38505091
[TBL] [Abstract][Full Text] [Related]
18. Organocatalytic enantioselective Pictet-Spengler approach to biologically relevant 1-benzyl-1,2,3,4-tetrahydroisoquinoline alkaloids.
Ruiz-Olalla A; Würdemann MA; Wanner MJ; Ingemann S; van Maarseveen JH; Hiemstra H
J Org Chem; 2015 May; 80(10):5125-32. PubMed ID: 25909585
[TBL] [Abstract][Full Text] [Related]
19. Phylogenetic analysis and functional characterization of norcoclaurine synthase involved in benzylisoquinoline alkaloids biosynthesis in Stephania tetrandra.
Li X; Li Q; Jiao X; Tang H; Cheng Y; Ma Y; Cui G; Tang J; Chen Y; Guo J; Huang L
J Cell Physiol; 2023 Jun; ():. PubMed ID: 37357496
[TBL] [Abstract][Full Text] [Related]
20. 'Dopamine-first' mechanism enables the rational engineering of the norcoclaurine synthase aldehyde activity profile.
Lichman BR; Gershater MC; Lamming ED; Pesnot T; Sula A; Keep NH; Hailes HC; Ward JM
FEBS J; 2015 Mar; 282(6):1137-51. PubMed ID: 25620686
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]