One-pot synthesis of functionalized beta-amino sulfides/beta-amino selenides via ring opening of cyclic sulfamidates

Venkateswarlu Cheerladinne; Datta Bandita; Chandrasekaran Srinivasan

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One-pot synthesis of functionalized beta-amino sulfides/beta-amino selenides via ring opening of cyclic sulfamidates

机译：通过环氨基磺酸盐的开环一锅合成功能化的β-氨基硫化物/β-氨基硒化物

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A number of functionalized beta-amino and gamma-amino sulfides and selenides have been synthesized involving a one-pot process of ring opening of cyclic sulfamidates with 'in situ' generated thiolate and selenoate species from diaryl disulfides and diphenyl diselenide using rongalite. A mild and efficient method has been developed for the synthesis of cysteines from serine.

机译：已经合成了许多功能化的β-氨基和γ-氨基硫化物和硒化物，涉及一锅法将环状氨基磺酸盐与二芳基二硫化物和二苯基二硒化物使用白锌矿“原位”生成的硫醇盐和硒酸酯物质开环开环。已经开发了一种温和而有效的方法，用于从丝氨酸合成半胱氨酸。

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《RSC Advances》 |2014年第81期|共5页
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Venkateswarlu Cheerladinne; Datta Bandita; Chandrasekaran Srinivasan;
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正文语种 eng
中图分类化学;
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1. One-pot synthesis of functionalized beta-amino sulfides/beta-amino selenides via ring opening of cyclic sulfamidates [J] . Venkateswarlu Cheerladinne, Datta Bandita, Chandrasekaran Srinivasan RSC Advances . 2014,第81期

机译：通过环氨基磺酸盐的开环一锅合成功能化的β-氨基硫化物/β-氨基硒化物
2. One-Pot Synthesis of beta-Amino/beta-Hydroxy Selenides and Sulfides from Aziridines and Epoxides [J] . Venkataraman Ganesh, Srinivasan Chandrasekaran Synthesis: International Journal of Methods in Synthetic Organic Chemistry . 2009,第19期

机译：从氮丙啶和环氧化物一锅法合成β-氨基/β-羟基硒化物和硫化物
3. Asymmetric synthesis of cyclic beta-amino acids and cyclic amines via sequential diastereoselective conjugate addition and ring closing metathesis [J] . Chippindale AM., Davies SG., Iwamoto K., Tetrahedron . 2003,第18期

机译：通过顺序非对映选择性共轭加成和闭环复分解反应合成环状β-氨基酸和环状胺
4. Peptidominetics:control of chemical shape.The synthesis of cyclic beta-amino acids using ring-closing metathesis [C] . Andrew D.Abell, James Gardiner European Peptide Symposium . 2002

机译：拟肽：化学形状的控制。利用环闭复分解的环状β-氨基酸的合成
5. Constrained beta-prolines. (I) Methanopyrrolidine beta-amino acids: Synthesis and chracterization of novel C6-substituted analogues and peptide oligomers. (II) Synthesis of 2,2-disubstituted pyrrolidine-3-carboxylic acids. [D] . Hu, Zilun. 2015

机译：受约束的β-脯氨酸。（I）甲基吡咯烷β-氨基酸：新型C6取代的类似物和肽低聚物的合成和表征。（II）2，2-二取代的吡咯烷-3-羧酸的合成。
6. Nickel-Catalyzed Asymmetric Hydrogenation of Cyclic Sulfamidate Imines: Efficient Synthesis of Chiral Cyclic Sulfamidates [O] . Yuanhua Liu, Zhiyuan Yi, Xuefeng Tan, 2019

机译：镍催化环状氨基磺酸亚胺的不对称氢化：手性环状氨基磺酸酯的高效合成
7. Enantioselective synthesis of cyclic beta-amino alcohols via tandem hydroalumination-cyclization-reduction of ethoxycarbonyl vinyl sulfoximines and application to the synthesis of potential aggrecanase inhibitors [O] . Acikalin Serdar 2009

机译：通过串联水铝化-环化-还原乙氧基羰基乙烯基亚砜亚胺的对映选择性合成环状β-氨基醇及其在潜在的聚集蛋白聚糖酶抑制剂的合成中的应用

One-pot synthesis of functionalized beta-amino sulfides/beta-amino selenides via ring opening of cyclic sulfamidates

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