These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
144 related articles for article (PubMed ID: 37091733)
1. Asymmetric synthesis of a stereopentade fragment toward latrunculins. Joyeux B; Gamet A; Casaretto N; Nay B Beilstein J Org Chem; 2023; 19():428-433. PubMed ID: 37091733 [TBL] [Abstract][Full Text] [Related]
2. Total syntheses of the actin-binding macrolides latrunculin A, B, C, M, S and 16-epi-latrunculin B. Fürstner A; De Souza D; Turet L; Fenster MD; Parra-Rapado L; Wirtz C; Mynott R; Lehmann CW Chemistry; 2007; 13(1):115-34. PubMed ID: 17091520 [TBL] [Abstract][Full Text] [Related]
3. Directed hydrogenations and an Ireland-Claisen rearrangement linked to evans-tishchenko chemistry: the highly efficient total synthesis of the marine cyclodepsipeptide doliculide. Chen T; Altmann KH Chemistry; 2015 Jun; 21(23):8403-7. PubMed ID: 25917788 [TBL] [Abstract][Full Text] [Related]
4. Remote Asymmetric Induction Reactions using a E, E-Vinylketene Silyl N, O-Acetal and the Wide Range Stereocontrol Strategy for the Synthesis of Polypropionates. Hosokawa S Acc Chem Res; 2018 May; 51(5):1301-1314. PubMed ID: 29726677 [TBL] [Abstract][Full Text] [Related]
5. Stereoselective construction of quaternary carbon stereocenters via a semipinacol rearrangement strategy. Wang B; Tu YQ Acc Chem Res; 2011 Nov; 44(11):1207-22. PubMed ID: 21728380 [TBL] [Abstract][Full Text] [Related]
7. Optimized Asymmetric Synthesis of Umuravumbolide. Pérez-Palau M; Balaguer-Garcia E; Romea P; Urpí F ACS Omega; 2022 Sep; 7(35):30835-30840. PubMed ID: 36092614 [TBL] [Abstract][Full Text] [Related]
8. Samarium Ion-Promoted Cross-Aldol Reactions and Tandem Aldol/Evans-Tishchenko Reactions. Lu L; Chang HY; Fang JM J Org Chem; 1999 Feb; 64(3):843-853. PubMed ID: 11674156 [TBL] [Abstract][Full Text] [Related]
9. Stereoselective Installation of Five Contiguous Stereogenic Centers in a Double Aldol-Tishchenko Cascade and Evaluation of the Key Transition State through DFT Calculation. Mackey P; Turlik A; Ando K; Light ME; Houk KN; McGlacken GP Org Lett; 2021 Aug; 23(16):6372-6376. PubMed ID: 34374288 [TBL] [Abstract][Full Text] [Related]
11. The domino multicomponent allylation reaction for the stereoselective synthesis of homoallylic alcohols. Tietze LF; Kinzel T; Brazel CC Acc Chem Res; 2009 Feb; 42(2):367-78. PubMed ID: 19154154 [TBL] [Abstract][Full Text] [Related]
12. Asymmetric Aldol-Tishchenko Reaction of Sulfinimines. Foley VM; McSweeney CM; Eccles KS; Lawrence SE; McGlacken GP Org Lett; 2015 Nov; 17(22):5642-5. PubMed ID: 26528888 [TBL] [Abstract][Full Text] [Related]
13. Latrunculins--novel marine macrolides that disrupt microfilament organization and affect cell growth: I. Comparison with cytochalasin D. Spector I; Shochet NR; Blasberger D; Kashman Y Cell Motil Cytoskeleton; 1989; 13(3):127-44. PubMed ID: 2776221 [TBL] [Abstract][Full Text] [Related]
14. Asymmetric Total Synthesis of the Gastroprotective Microbial Agent AI-77-B. Ghosh AK; Bischoff A; Cappiello J European J Org Chem; 2003 Mar; 2003(5):821-832. PubMed ID: 30393460 [TBL] [Abstract][Full Text] [Related]
15. Synthesis of the C4-C16 Polyketide Fragment of Portimines A and B. Ding XB; Aitken HRM; Pearl ES; Furkert DP; Brimble MA J Org Chem; 2021 Sep; 86(18):12840-12850. PubMed ID: 34469687 [TBL] [Abstract][Full Text] [Related]
16. Stereoselective Synthesis of 2-Fluoro-1,3-Diols via Lithium Binaphtholate-Catalyzed Aldol-Tishchenko Reaction. Asano T; Kotani S; Nakajima M Org Lett; 2019 Jun; 21(11):4192-4196. PubMed ID: 31120256 [TBL] [Abstract][Full Text] [Related]
17. Synthesis of solandelactone F, constanolactone A and an advanced intermediate towards solandelactone E from a common synthetic intermediate. Yalla R; Raghavan S Org Biomol Chem; 2019 May; 17(18):4572-4592. PubMed ID: 30997906 [TBL] [Abstract][Full Text] [Related]
18. Catalyst-controlled asymmetric synthesis of fostriecin and 8-epi-fostriecin. Maki K; Motoki R; Fujii K; Kanai M; Kobayashi T; Tamura S; Shibasaki M J Am Chem Soc; 2005 Dec; 127(48):17111-7. PubMed ID: 16316259 [TBL] [Abstract][Full Text] [Related]
19. Studies on the synthesis of the inostamycin natural products: a reductive aldol/reductive Claisen approach to the C10-C24 ketone fragment. Fuller NO; Morken JP Org Lett; 2005 Oct; 7(22):4867-9. PubMed ID: 16235909 [TBL] [Abstract][Full Text] [Related]
20. Asymmetric synthesis of the highly potent anti-metastatic prostacyclin analogue cicaprost and its isomer isocicaprost. Lerm M; Gais HJ; Cheng K; Vermeeren C J Am Chem Soc; 2003 Aug; 125(32):9653-67. PubMed ID: 12904032 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]