A variation of the Pictet-Spengler reaction via a sequential reduction-cyclization reaction of N-acylcarbamates: synthesis of 1-substituted tetrahydroisoquinoline derivatives
A new variation of the Pictet-Spengler reaction for the synthesis of 1-substituted tetrahydroisoquinoline derivatives has been developed. The reaction employs the reduction of N-acylcarbamates by DIBAL-H followed by simultaneous cyclization mediated by BF3·OEt2. The synthetic potential of this metho...
محفوظ في:
المؤلفون الرئيسيون: | Chutima Kuhakarn, Nattakan Panyachariwat, Somsak Ruchirawat |
---|---|
مؤلفون آخرون: | Chulabhorn Research Institute |
التنسيق: | مقال |
منشور في: |
2018
|
الموضوعات: | |
الوصول للمادة أونلاين: | https://repository.li.mahidol.ac.th/handle/123456789/24083 |
الوسوم: |
إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
|
المؤسسة: | Mahidol University |
مواد مشابهة
-
The N-acyliminium Pictet-Spengler condensation as a multicomponent combinatorial reaction on solid phase and its application to the synthesis of demethoxyfumitremorgin C analogues
بواسطة: Wang, H., وآخرون
منشور في: (2014) -
Solid-phase synthesis of structurally diverse heterocycles by an amide-ketone condensation/N-acyliminium Pictet-Spengler sequence
بواسطة: Givskov, Michael, وآخرون
منشور في: (2013) -
Triflic-acid-catalyzed tandem allylic substitution–cyclization reaction of alcohols with thiophenols—facile access to polysubstituted thiochromans
بواسطة: Abdul Sadeer, وآخرون
منشور في: (2019) -
Reductive cyclization and petasis-like reaction for the synthesis of functionalized γ-lactams
بواسطة: Wu, Peng, وآخرون
منشور في: (2015) -
Novel triazole-tetrahydroisoquinoline hybrids as human aromatase inhibitors
بواسطة: Chanamon Chamduang, وآخرون
منشور في: (2020)