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在复杂碳水化合物合成中,糖端基中心的临时醚保护基。

Temporary ether protecting groups at the anomeric center in complex carbohydrate synthesis.

机构信息

Department of Medicinal Chemistry, School of Pharmacy, China Pharmaceutical University, Nanjing, China.

State Key Laboratory of Bio-organic and Natural Products Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, China.

出版信息

Adv Carbohydr Chem Biochem. 2020;77:1-69. doi: 10.1016/bs.accb.2019.10.001. Epub 2020 Mar 2.

Abstract

The synthesis of a carbohydrate building block usually starts with introduction of a temporary protecting group at the anomeric center and ends with its selective cleavage for further transformation. Thus, the choice of the anomeric temporary protecting group must be carefully considered because it should retain intact during the whole synthetic manipulation, and it should be chemoselectively removable without affecting other functional groups at a late stage in the synthesis. Etherate groups are the most widely used temporary protecting groups at the anomeric center, generally including allyl ethers, MP (p-methoxyphenyl) ethers, benzyl ethers, PMB (p-methoxybenzyl) eithers, and silyl ethers. This chapter provides a comprehensive review on their formation, cleavage, and applications in the synthesis of complex carbohydrates.

摘要

碳水化合物砌块的合成通常从在糖苷中心引入临时保护基团开始,最后通过选择性裂解来进行进一步的转化。因此,必须仔细考虑选择糖苷位临时保护基团,因为它在整个合成过程中应保持完整,并且应在合成后期的后期通过化学选择性去除而不影响其他官能团。醚基是在糖苷中心最广泛使用的临时保护基团,通常包括烯丙基醚、MP(对甲氧基苯基)醚、苄基醚、PMB(对甲氧基苄基)醚和硅基醚。本章全面综述了它们的形成、裂解及其在复杂碳水化合物合成中的应用。

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