γ-Regioselective Functionalization of 3-Alkenylindoles via 1,6-Addition to Extended Alkylideneindolenine Intermediates
出版年份 2018 全文链接
标题
γ-Regioselective Functionalization of 3-Alkenylindoles via
1,6-Addition to Extended Alkylideneindolenine Intermediates
作者
关键词
-
出版物
ADVANCED SYNTHESIS & CATALYSIS
Volume 360, Issue 6, Pages 1296-1302
出版商
Wiley
发表日期
2018-02-01
DOI
10.1002/adsc.201701558
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- 2- and 3-Vinylindoles as 4π Components in Cycloaddition Reactions
- (2017) Elisabetta Rossi et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
- Indolylmethanols as Reactants in Catalytic Asymmetric Reactions
- (2017) Guang-Jian Mei et al. JOURNAL OF ORGANIC CHEMISTRY
- The Application of N-Protected 3-Vinylindoles in Chiral Phosphoric Acid-Catalyzed [3+2] Cyclization with 3-Indolylmethanols: Monoactivation of the Catalyst to Vinyliminium
- (2016) Tao Fan et al. ADVANCED SYNTHESIS & CATALYSIS
- Use of a Catalytic Chiral Leaving Group for Asymmetric Substitutions at sp3 -Hybridized Carbon Atoms: Kinetic Resolution of β-Amino Alcohols by p -Methoxybenzylation
- (2016) Yusuke Kuroda et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Sulfonyl Azoles in the Synthesis of 3-Functionalized Azole Derivatives
- (2016) Alessandro Palmieri et al. CHEMICAL RECORD
- Synthesis of α-functionalized α-indol-3-yl carbonyls through direct SN reactions of indol-3-yl α-acyloins
- (2016) Anisley Suárez et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- Fluorinated alcohol-mediated [4 + 3] cycloaddition reaction of indolyl alcohols with cyclopentadiene
- (2016) Jian Liu et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- Organocatalytic Highly Enantioselective Substitution of 3-(1-Tosylalkyl)indoles with Oxindoles Enables the First Total Synthesis of (+)-Trigolutes B
- (2015) Jian-Zhou Huang et al. CHEMISTRY-A EUROPEAN JOURNAL
- Enantioselective Synthesis of Piperidines through the Formation of Chiral Mixed Phosphoric Acid Acetals: Experimental and Theoretical Studies
- (2014) Zhankui Sun et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Alkylideneindoleninium Ions and Alkylideneindolenines: Key Intermediates for the Asymmetric Synthesis of 3-Indolyl Derivatives
- (2014) Liang Wang et al. Asian Journal of Organic Chemistry
- Palladium(II)-Catalyzed Efficient C-3 Functionalization of Indoles with Benzylic and Allylic Alcohols under Co-Catalyst, Acid, Base, Additive and External Ligand-Free Conditions
- (2013) Debjit Das et al. ADVANCED SYNTHESIS & CATALYSIS
- When asymmetric aminocatalysis meets the vinylogy principle
- (2013) Igor D. Jurberg et al. CHEMICAL COMMUNICATIONS
- Catalytic Asymmetric Aza-Diels–Alder Reactions: The Povarov Cycloaddition Reaction
- (2013) Mariafrancesca Fochi et al. SYNTHESIS-STUTTGART
- Aminocatalytic remote functionalization strategies
- (2013) Hao Jiang et al. Chemical Science
- First example of a heterobimetallic ‘Pd–Sn’ catalyst for direct activation of alcohol: efficient allylation, benzylation and propargylation of arenes, heteroarenes, active methylenes and allyl-Si nucleophiles
- (2012) Debjit Das et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- The Vinylogous Aldol and Related Addition Reactions: Ten Years of Progress†
- (2011) Giovanni Casiraghi et al. CHEMICAL REVIEWS
- The Organocatalytic Vinylogous Aldol Reaction: Recent Advances
- (2011) Sunil V. Pansare et al. CHEMISTRY-A EUROPEAN JOURNAL
- Synthesis of 3-substituted indoles via reactive alkylideneindolenine intermediates
- (2009) Alessandro Palmieri et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- Advances in Exploring Heterocyclic Dienoxysilane Nucleophiles in Asymmetric Synthesis
- (2009) Giovanni Casiraghi et al. SYNLETT
- Asymmetric Brønsted Acid Catalysis: Enantioselective Nucleophilic Substitutions and 1,4-Additions
- (2007) Magnus Rueping et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started