Synthesis of new enantiomerically pure β-amino alcohols of the pinane series

L. L. Frolova; D. V. Sudarikov; I. N. Alekseev; O. A. Banina; P. A. Slepukhin; A. V. Kutchin

doi:10.1134/S1070428017030046

Synthesis of new enantiomerically pure β-amino alcohols of the pinane series

作者: Frolova L.L.¹, Sudarikov D.V.¹, Alekseev I.N.¹, Banina O.A.¹, Slepukhin P.A.²^,3, Kutchin A.V.¹
隶属关系:
1. Institute of Chemistry, Komi Scientific Center, Ural Branch
2. Postovskii Institute of Organic Synthesis, Ural Branch
3. Yeltsin Ural Federal University
期: 卷 53, 编号 3 (2017)
页面: 335-343
栏目: Article
URL: https://journal-vniispk.ru/1070-4280/article/view/215878
DOI: https://doi.org/10.1134/S1070428017030046
ID: 215878

如何引用文章

全文:

开放存取

##reader.subscriptionAccessGranted##
受限制的访问

订阅存取

详细
作者简介
参考
补充文件
统计

详细

A series of new β-amino alcohols with pinane structure, (+)- and (‒)-3α-amino-10β-pinan-4β-ols, 4β-amino-10β-pinan-3α-ol, and 4α-amino-10β-pinan-3α-ol have been synthesized with the goal of using them as organocatalysts in the aldol reaction of isatin with acetone.