Progress, challenges and future directions of heterocycles as building blocks in iterative methodologies towards sequence-defined oligomers and polymers
文献信息
Stephen A. Hill, Robert Steinfort, Laura Hartmann
The synthesis of sequence-defined oligomers and polymers is an important contemporary research topic due to the potential for creating materials with function tailored directly into the primary structure. Sequence-defined materials have so far been applied to biomimicry, data storage and sensing. Heterocyclic building blocks such as thiolactones and epoxides are key building blocks for producing sequence-defined macromolecules using iterative methodologies. In this review we critically evaluate: the current literature on different heterocyclic strategies using solid- or solution-phase methods for the iterative synthesis of sequence-defined polymers; the challenges surrounding these systems; and the potential future direction of heterocycles, so far not used in this field.
相关文献
Unprecedented steric deformation of ortho-carborane
Brian W. Hutton, Fraser MacIntosh, David Ellis, Fabien Herisse, Stuart A. Macgregor, David McKay, Victoria Petrie-Armstrong, Georgina M. Rosair, Dmitry S. Perekalin, Hugo Tricas, Alan J. Welch
DOI: 10.1039/B810702E
Facile construction of functionalized 4H-chromenevia tandem benzylation and cyclization
Jinmin Fan, Zhiyong Wang
DOI: 10.1039/B812046C
Orthogonal or simultaneous use of disulfide and hydrazone exchange in dynamic covalent chemistry in aqueous solution
Zaida Rodriguez-Docampo
DOI: 10.1039/B808725C
Facile preparation of low cytotoxicity fluorescent carbon nanocrystals by electrooxidation of graphite
Qiao-Ling Zhao, Zhi-Ling Zhang, Bi-Hai Huang, Jun Peng, Min Zhang, Dai-Wen Pang
DOI: 10.1039/B812420E
Covalent double level dynamic combinatorial libraries: selectively addressable exchange processes
A. Gastón Orrillo, Andrea M. Escalante, Ricardo L. E. Furlan
DOI: 10.1039/B808565J
A total loss of innocence: double ortho-metallation of bis(triphenylphosphano)iminium cation, [N(PPh3)2]+, by tris(η-naphthalene)tantalate(1−)‡
Victor J. Sussman, John E. Ellis
DOI: 10.1039/B811320C
Greatly reduced amino acid alphabets in directed evolution: making the right choice for saturation mutagenesis at homologous enzyme positions
Manfred T. Reetz, Sheng Wu
DOI: 10.1039/B813388C
Non-hydrolytic synthesis of mesoporous silica–titania catalysts for the mild oxidation of sulfur compounds with hydrogen peroxide
P. Hubert Mutin, Emil Dumitriu, François Fajula, André Vioux, Vasile Hulea
DOI: 10.1039/B811668G
Amino-sugar modular ligands—useful cores for the formation of asymmetric copper 1,4-addition catalysts
Antonella De Roma, Francesco Ruffo, Simon Woodward
DOI: 10.1039/B813137F
Facile synthesis of aminophenylboronic acid-functionalized magnetic nanoparticles for selective separation of glycopeptides and glycoproteins
Wei Zhou, Ning Yao, Guoping Yao, Chunhui Deng, Xiangmin Zhang, Pengyuan Yang
DOI: 10.1039/B808800D
您可能还喜欢
2-氨基-2-(5-甲基噻吩-2-基)乙酸(CAS号:89776-66-9)应用于哪些行业?
2-氨基-2-(5-甲基噻吩-2-基)乙酸主要应用于医药、聚合物、传感器和半导体等行业。在医药领域,它作为中间体用于合成各种药物。在聚合物行业,它可以用作稳定剂...
什么是N-(叔丁氧羰基)-3-碘吲唑(CAS号:290368-00-2)?
N-(叔丁氧羰基)-3-碘吲唑是一种化学化合物,其英文名称为2-Methyl-2-propanyl 3-iodo-1H-indazole-1-carboxyla...
N-芴甲氧羰基-D-谷氨酸(CAS号:104091-09-0)的市场或研究趋势如何?
该化合物作为重要的保护基,广泛应用于生物有机化学合成中,尤其在肽类、蛋白质和寡核苷酸的研究领域。随着合成生物学和药物开发的进展,该化合物的需求持续增长。未来的研...
2-乙氧基-1-萘酰氯(CAS号:55150-29-3)的市场或研究趋势如何?
2-乙氧基-1-萘酰氯在研究领域中主要用于合成研究和有机化学反应,随着有机合成技术的发展,其市场应用和研究兴趣可能会有所增长。尤其是在新型药物合成和新材料开发领...
1-甲氧基菜豆素(CAS号:65428-13-9)的主要用途是什么?
1-甲氧基菜豆素主要应用于有机合成、药物化学领域,作为合成其他有机化合物的中间体或前体。此外,由于其特殊的化学性质,也可能用于某些特定的化学研究和实验中。
small>-2-氨基丁酸(CAS号:106873-99-8)的主要用途是什么?
small>-2-氨基丁酸主要应用于有机合成和化学研究中,作为中间体或试剂使用。此外,它还可能用于某些药物合成过程中。
什么是5-氨基-2-氯-n-(2-呋喃甲基)苯甲酰胺(CAS号:926216-59-3)?
5-氨基-2-氯-n-(2-呋喃甲基)苯甲酰胺是一种有机化合物,其分子式为C11H9ClN3O。它具有一定的生物活性,在合成化学和药物化学中有一定的应用价值。
4-(3-溴苯甲酰基)-哌嗪-1-羧酸叔丁酯(CAS号:890153-34-1)适用哪些法规指南?
该化合物根据其化学性质和用途,可能需要符合GHS(全球化学品统一分类和标签制度)的分类标准,包括急性毒性、皮肤腐蚀/刺激、严重眼损伤/眼刺激等类别。此外,根据其...
如何储存(9ci)-2,4-二甲基-1H-吡咯-3-甲腈(CAS号:26187-28-0)?
应将(9ci)-2,4-二甲基-1H-吡咯-3-甲腈存放在阴凉、干燥的地方,避免阳光直射。储存容器应密封良好,防止挥发和污染。建议温度保持在20-25℃之间,湿...
巨大戟醇-5,20-缩丙酮-3-当归酸酯(CAS号:87980-68-5)通常如何合成?
该化合物通常通过合成当归酸酯的方法制备,具体步骤为将当归酸酯与巨大戟醇-5,20-缩丙酮进行缩合反应,反应条件为温和的酸性环境,通常使用三氟乙酸作为催化剂。该合...
来源期刊
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.











![4-Penten-1-yl 2-[(2-furylmethyl)(1H-imidazol-1-ylcarbonyl)amino]butanoate structure 4-Penten-1-yl 2-[(2-furylmethyl)(1H-imidazol-1-ylcarbonyl)amino]butanoate structure](https://cnstatic.chemtradehub.com/structs/101/101903-30-4-ac34.webp)
![(3R)-4-(4-Chlorophenyl)-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)butanoic acid structure (3R)-4-(4-Chlorophenyl)-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)butanoic acid structure](https://cnstatic.chemtradehub.com/structs/218/218608-96-9-f871.webp)

