Total synthesis of celogentin C.
作者信息
Ma Bing, Litvinov Dmitry N, He Liwen, Banerjee Biplab, Castle Steven L
机构信息
Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, USA.
出版信息
Angew Chem Int Ed Engl. 2009;48(33):6104-7. doi: 10.1002/anie.200902425.
Abstract
摘要
相似文献
1
Total synthesis of celogentin C.西洛津汀C的全合成。
Angew Chem Int Ed Engl. 2009;48(33):6104-7. doi: 10.1002/anie.200902425.
2
Total synthesis of cryptophycin analogues via a scaffold approach.通过支架法全合成隐藻素类似物。
Org Lett. 2006 Jul 6;8(14):2993-6. doi: 10.1021/ol0609356.
3
Total synthesis of celogentin C by stereoselective C-H activation.通过立体选择性C-H活化全合成塞洛琴汀C
Angew Chem Int Ed Engl. 2010;49(5):958-61. doi: 10.1002/anie.200905134.
4
Synthesis and structure-activity relationships of 1-benzyl-4,5,6-trimethoxyindoles as a novel class of potent antimitotic agents.新型强效抗有丝分裂剂1-苄基-4,5,6-三甲氧基吲哚的合成及其构效关系
ChemMedChem. 2009 Apr;4(4):588-93. doi: 10.1002/cmdc.200800405.
5
Stereocontrolled and efficient total synthesis of (-)-stephanotic acid methyl ester and (-)-celogentin C.立体控制和高效全合成 (-)-stephanotic 酸甲酯和 (-)-celogentin C。
Org Lett. 2010 Mar 5;12(5):956-9. doi: 10.1021/ol902944f.
6
Synthesis and biological evaluation of 1-methyl-2-(3',4',5'-trimethoxybenzoyl)-3-aminoindoles as a new class of antimitotic agents and tubulin inhibitors.新型抗有丝分裂剂和微管蛋白抑制剂1-甲基-2-(3',4',5'-三甲氧基苯甲酰基)-3-氨基吲哚的合成及生物学评价
J Med Chem. 2008 Mar 13;51(5):1464-8. doi: 10.1021/jm7011547. Epub 2008 Feb 9.
7
Novel carbazole and acyl-indole antimitotics.新型咔唑和酰基吲哚抗有丝分裂剂。
Bioorg Med Chem Lett. 2009 Jun 1;19(11):3078-80. doi: 10.1016/j.bmcl.2009.04.010. Epub 2009 Apr 9.
8
Divergent total synthesis of the antimitotic agent leiodermatolide.抗有丝分裂剂leiodermatolide的发散式全合成。
Angew Chem Int Ed Engl. 2012 Nov 26;51(48):12041-6. doi: 10.1002/anie.201206670. Epub 2012 Oct 18.
9
Synthesis of the celogentin C right-hand ring.塞洛京汀C右手环的合成。
Org Lett. 2006 Mar 16;8(6):1165-8. doi: 10.1021/ol060016f.
10
Total synthesis of the antimitotic bicyclic peptide celogentin C.Celogentin C 类抗有丝分裂双环肽的全合成。
J Am Chem Soc. 2010 Jan 27;132(3):1159-71. doi: 10.1021/ja909870g.
引用本文的文献
1
Development of a Diastereoselective Csp-Csp Cross-Coupling Reaction Inspired by Macrocyclic RiPP Natural Products.受大环核糖体肽天然产物启发的非对映选择性Csp-Csp交叉偶联反应的开发
Org Lett. 2025 Jul 18;27(28):7627-7632. doi: 10.1021/acs.orglett.5c02198. Epub 2025 Jul 9.
2
Biocompatible strategies for peptide macrocyclisation.用于肽大环化的生物相容性策略。
Chem Sci. 2024 Jan 5;15(7):2300-2322. doi: 10.1039/d3sc05738k. eCollection 2024 Feb 14.
3
Recent Advances in the Synthesis of 3,n-Fused Tricyclic Indole Skeletons via Palladium-Catalyzed Domino Reactions.钯催化的多米诺反应在 3,n-稠合三环吲哚骨架合成中的最新进展。
Molecules. 2023 Feb 8;28(4):1647. doi: 10.3390/molecules28041647.
4
Solid-phase total synthesis and structural confirmation of antimicrobial longicatenamide A.抗菌长链酰胺A的固相全合成及结构确证
Beilstein J Org Chem. 2022 Nov 18;18:1560-1566. doi: 10.3762/bjoc.18.166. eCollection 2022.
5
Synthesis of Ribosomally Synthesized and Post-Translationally Modified Peptides Containing C-C Cross-Links.含 C-C 交叉键的核糖体合成和翻译后修饰肽的合成。
J Nat Prod. 2022 Oct 28;85(10):2519-2539. doi: 10.1021/acs.jnatprod.2c00508. Epub 2022 Sep 22.
6
Convergent Total Synthesis of Yaku'amide A.雅库酰胺 A 的会聚全合成。
Angew Chem Int Ed Engl. 2021 Mar 1;60(10):5162-5167. doi: 10.1002/anie.202014238. Epub 2021 Jan 21.
7
Base-Promoted Synthesis of β-Substituted-Tryptophans via a Simple and Convenient Three-Component Condensation of Nickel(II) Glycinate.通过甘氨酸镍（II）简单便捷的三组分缩合反应实现碱促进的β-取代色氨酸的合成。
Molecules. 2017 Apr 27;22(5):695. doi: 10.3390/molecules22050695.
8
Scalable total syntheses of N-linked tryptamine dimers by direct indole-aniline coupling: psychotrimine and kapakahines B and F.通过直接吲哚-苯胺偶联实现 N-连接色胺二聚体的可扩展全合成：psychotrimine 和 kapakahines B 和 F。
J Am Chem Soc. 2010 May 26;132(20):7119-37. doi: 10.1021/ja1009458.
9
Total synthesis of the antimitotic bicyclic peptide celogentin C.Celogentin C 类抗有丝分裂双环肽的全合成。
J Am Chem Soc. 2010 Jan 27;132(3):1159-71. doi: 10.1021/ja909870g.
本文引用的文献
1
Second-generation DBFOX ligands for the synthesis of beta-substituted alpha-amino acids via enantioselective radical conjugate additions.用于通过对映选择性自由基共轭加成反应合成β-取代α-氨基酸的第二代DBFOX配体。
J Org Chem. 2008 Nov 21;73(22):8973-8. doi: 10.1021/jo801721z. Epub 2008 Oct 24.
2
Total synthesis of stephanotic acid methyl ester.千金藤酸甲酯的全合成。
Org Lett. 2006 May 11;8(10):1975-8. doi: 10.1021/ol060153c.
3
Synthesis of the celogentin C right-hand ring.塞洛京汀C右手环的合成。
Org Lett. 2006 Mar 16;8(6):1165-8. doi: 10.1021/ol060016f.
4
Synthesis of beta-substituted alpha-amino acids via Lewis acid promoted enantioselective radical conjugate additions.通过路易斯酸促进的对映选择性自由基共轭加成反应合成β-取代的α-氨基酸
J Org Chem. 2005 Sep 30;70(20):8140-7. doi: 10.1021/jo051334f.
5
Asymmetric synthesis of the central tryptophan residue of stephanotic acid.斯氏酸中心色氨酸残基的不对称合成。
Org Biomol Chem. 2004 Dec 21;2(24):3545-7. doi: 10.1039/b414996c. Epub 2004 Nov 3.
6
Synthesis of beta-substituted alpha-amino acids via Lewis acid promoted radical conjugate additions to alpha,beta-unsaturated alpha-nitro esters and amides.通过路易斯酸促进的自由基共轭加成反应，向α,β-不饱和α-硝基酯和酰胺合成β-取代的α-氨基酸。
Org Lett. 2004 Feb 5;6(3):449-52. doi: 10.1021/ol036461h.
7
Catalytic asymmetric synthesis of the central tryptophan residue of celogentin C.塞洛根汀C中心色氨酸残基的催化不对称合成。
Org Lett. 2003 Oct 2;5(20):3611-4. doi: 10.1021/ol035236x.
8
Celogentins A-C, new antimitotic bicyclic peptides from the seeds of Celosia argentea.鸡冠花素A - C，从鸡冠花种子中提取的新型抗有丝分裂双环肽。
J Org Chem. 2001 Oct 5;66(20):6626-33. doi: 10.1021/jo0103423.
9
Computer-assisted structure determination. Structure Of the peptide moroidin from laportea moroides.计算机辅助结构测定。来自咬人荨麻的肽类物质moroidin的结构。
J Org Chem. 2000 Dec 1;65(24):8406. doi: 10.1021/jo004021n.
10
Stephanotic acid, a novel cyclic pentapeptide from the stem of Stephanotis floribunda.络石氨酸，一种从多花络石茎中提取的新型环状五肽。
J Nat Prod. 2000 Apr;63(4):540-2. doi: 10.1021/np990532x.
Zotero 插件