A NEW STEREOCONTROLLED APPROACH TO A KEY INTERMEDIATE IN THE SYNTHESIS OF (2S,3R)-CAPREOMYCIDINE

Miroslava MARTINKOVA; Jozef GONDA; Martina DZOGANOVA

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A NEW STEREOCONTROLLED APPROACH TO A KEY INTERMEDIATE IN THE SYNTHESIS OF (2S,3R)-CAPREOMYCIDINE

机译：（2S，3R）-己内酰胺合成中关键中间体的新立体控制方法

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A new stereocontrolled approach to the synthesis of advanced intermediate in the synthesis of nonproteinogenic amino acid (2S,3R)-capreomycidine via the novel domino reaction has been developed.

机译：已开发了一种通过新型多米诺反应合成非中间体氨基酸（2S，3R）-环胞嘧啶核苷的先进中间体合成的立体控制新方法。

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《Collection of Czechoslovak Chemical Communications》 |2006年第8期|共12页
作者
Miroslava MARTINKOVA; Jozef GONDA; Martina DZOGANOVA;
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正文语种 eng
中图分类化学;
关键词
Capreomycidine; Capreomycins; Stereoselectivity; Nonproteinogenic amino acids; 3; 3-Sigmatropic rearrangements; Total synthesis;

机译：Capreomycidine;Capreomycins;立体选择性;非蛋白氨基酸;[3;3]-嗜适性重排;总合成;

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1. A NEW STEREOCONTROLLED APPROACH TO A KEY INTERMEDIATE IN THE SYNTHESIS OF (2S,3R)-CAPREOMYCIDINE [J] . Miroslava MARTINKOVA, Jozef GONDA, Martina DZOGANOVA Collection of Czechoslovak Chemical Communications . 2006,第8期

机译：（2S，3R）-己内酰胺合成中关键中间体的新立体控制方法
2. The asymmetric synthesis of (2S,3R)-capreomycidine [J] . Duane E.DeMong, Robret M.Williams Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry . 2001,第21期

机译：（2S，3R）-己内酰胺的不对称合成
3. Concise Synthesis of (2S,3R)-3-Hydroxy-2-phenylpiperidine: An AdvancedKey Intermediate of Human Non-Peptide NK-1 Receptor Antagonists [J] . Benoit Mal, Franck Ferreira, Candice Botuha, Synlett . 2009,第19期

机译：简明合成（2S，3R）-3-羟基-2-苯基哌啶：人类非肽NK-1受体拮抗剂的高级关键中间体。
4. Asymmetric synthesis of fully protected (2S,3R)-N-(1',1'-di-methylallyl)-3-hydroxytryptopahan,a new amino acid found in anti-inflammatory cyclic peptide cyclomarin C [C] . Zhu-Jun Yao, Shi-Jun Wen European Peptide Symposium . 2002

机译：完全保护的不对称合成（2S，3R）-N-（1'，1'-二甲基ally1）-3-羟基特普坦，在抗炎环肽环甘油蛋白C中发现的新氨基酸
5. The asymmetric synthesis of (2S,3R)-capreomycidine and the total synthesis of capreomycin IB. [D] . DeMong, Duane Eugene. 2003

机译：（2S，3R）-capreomycidine的不对称合成和capreomycin IB的总合成。
6. Enantioselective Synthesis of (2R 3S)- and (2S 3R)-444-trifluoro-N-Fmoc-O-tert-butyl-threonine and their Racemization-free Incorporation into Oligopeptides via Solid-phase Synthesis [O] . Nu Xiao, Zhong-Xing Jiang, Y. Bruce Yu -1

机译：（2R3S）-和（2S3R）-444-三氟-N-Fmoc-O-叔丁基苏氨酸的对映选择性合成及其通过固相合成将其无消旋地引入寡肽
7. Highly stereocontrolled total synthesis of the polyether antibiotic salinomycin. IV. Chemical degradation of salinomycin for the structure confirmation of synthetic key intermediates. [O] . Kiyoshi HORITA, Satoshi NAGATO, Yuji OIKAWA, 1989

机译：高度立体控制聚醚抗生素盐霉素的总合成。 IV。合成密钥中间体结构确认盐霉素的化学降解。

A NEW STEREOCONTROLLED APPROACH TO A KEY INTERMEDIATE IN THE SYNTHESIS OF (2S,3R)-CAPREOMYCIDINE

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