AN ENANTIOSELECTIVE SYNTHESIS OF 1-AZASPIRO[5.5]-UNDECANE RING SYSTEM OF HISTRIONICOTOXIN ALKALOIDS FROM D(+)-GLUCOSE

Smritilekha Bera

首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >AN ENANTIOSELECTIVE SYNTHESIS OF 1-AZASPIRO[5.5]-UNDECANE RING SYSTEM OF HISTRIONICOTOXIN ALKALOIDS FROM D(+)-GLUCOSE

【24h】

AN ENANTIOSELECTIVE SYNTHESIS OF 1-AZASPIRO[5.5]-UNDECANE RING SYSTEM OF HISTRIONICOTOXIN ALKALOIDS FROM D(+)-GLUCOSE

机译：从D（+）-葡萄糖对映体合成1-氮杂螺[5.5]-十一烷环的Hisionicotoxin碱的对映体。

获取原文

获取原文并翻译 | 示例

获取外文期刊封面封底 >>

开具论文收录证明 >>

文献代查 >>

页面导航

摘要
著录项
相似文献
相关主题

摘要

Abstract- The preparation of l-azaspiro[5.5]undecane ring system common to histrionicotoxin alkaloids has been accomplished from D-glucose diacetonide.

机译：摘要-由D-葡萄糖二丙酮化物完成了组氨酸毒素生物碱共有的L-氮杂螺[5.5]十一烷环系统的制备。

著录项

来源
《Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry》 |2005年第12期|共16页
作者
Smritilekha Bera;
展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种 eng
中图分类杂环化合物;
关键词

相似文献

外文文献
中文文献
专利

1. AN ENANTIOSELECTIVE SYNTHESIS OF 1-AZASPIRO[5.5]-UNDECANE RING SYSTEM OF HISTRIONICOTOXIN ALKALOIDS FROM D(+)-GLUCOSE [J] . Smritilekha Bera Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry . 2005,第12期

机译：从D（+）-葡萄糖对映体合成1-氮杂螺[5.5]-十一烷环的Hisionicotoxin碱的对映体。
2. Efficient Approaches toward the Solid-Phase Synthesis of New Heterocyclic Azoniaspiro Ring Systems:Synthesis of Tri- and Tetrasubstituted 10-Oxo-3,9-diaza-6-azoniaspiro[5.5]undecanes [J] . Adel Nefzi, Rodegar T.Santos The Journal of Organic Chemistry . 2005,第23期

机译：新型杂环氮杂螺环体系固相合成的有效方法：三和四取代的10-Oxo-3,9-diaza-6-氮杂螺环[5.5]十一烷的合成
3. A Stereoselective Approach to the Azaspiro[5.5]undecane Ring System Using a Conjugate Addition/Dipolar Cycloaddition Cascade: Application to the Total Synthesis of (+/-)-2,7,8-epi-Perhydrohistrionicotoxin [J] . Wilson MS, Padwa A The Journal of Organic Chemistry . 2008,第24期

机译：一种使用共轭加成/偶极环加成级联的叠氮[5.5]十一烷环系的立体选择方法：在（+/-）-2,7,8-epi-Perhydrohistrionicotoxin的总合成中的应用
4. SYNTHESIS OF THE OPTICALLY ACTIVE FORMS OF 4,10-DIHYDROXY-1,7-DIOXASPIRO 5,5 UNDECANE AND THEIR CONVERSION TO THE ENANTIOMERS OF 1,7-DIOXASPIRO5.5UNDECANE, THE OLIVE FLY PHEROMONE [C] . T. Uematsu, K.Mori International Congress of Pesticide Chemistry . 1986

机译：合成4,10-二羟基-1,7-Dioxaspiro 5,5的非甲烷的光学活性形式及其转化为1,7-二氧化硅的对映体5.5未甲烷，橄榄蝇信息素
5. Synthetic applications of the type 2 intramolecular Diels-Alder reaction: (1) Efforts toward the total synthesis of the welwitindolinone alkaloids and (2) Enantioselective synthesis of bridged bicyclic ring systems. [D] . Brailsford, John A. 2009

机译：2型分子内Diels-Alder反应的合成应用：（1）努力实现welwitindolinone生物碱的全合成，以及（2）桥联双环系统的对映选择性合成。
6. Erratum: Antonsen S.; et al. Synthesis of Racemic β-Chamigrene a Spiro5.5undecane Sequiterpene. Molecules 2014 19 20664–20670 [O] . 2018

机译：勘误表：AntonsenS .;等外消旋β-Chamigrene尖顶5.5十一碳七萜烯的合成。分子20141920664-20670
7. Formal total synthesis of histrionicotoxin alkaloids via Hg(OTf)2-catalyzed cycloisomerization and SmI2-induced ring expansion [O] . Kunihiro Matsumura, Keisuke Nishikawa, Hiroaki Yoshida, 2018

机译：通过Hg（OTF）2催化的环旋异构化和SMI2诱导环膨胀的正式合成母生素毒素生物碱

AN ENANTIOSELECTIVE SYNTHESIS OF 1-AZASPIRO[5.5]-UNDECANE RING SYSTEM OF HISTRIONICOTOXIN ALKALOIDS FROM D(+)-GLUCOSE

摘要

著录项

相似文献

相关主题

期刊订阅