Enantioselective total synthesis of (+)-methoxystemofoline and (+)-isomethoxystemofoline
出版年份 2015 全文链接
标题
Enantioselective total synthesis of (+)-methoxystemofoline and (+)-isomethoxystemofoline
作者
关键词
-
出版物
CHEMICAL COMMUNICATIONS
Volume 51, Issue 22, Pages 4576-4578
出版商
Royal Society of Chemistry (RSC)
发表日期
2015-01-08
DOI
10.1039/c4cc09598g
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。- Complexity generation by chemical synthesis: a five-step synthesis of (−)-chaetominine from l-tryptophan and its biosynthetic implications
- (2014) Chu-Pei Xu et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- Versatile construction of functionalized tropane ring systems based on lactam activation: enantioselective synthesis of (+)-pervilleine B
- (2013) Su-Yu Huang et al. CHEMICAL COMMUNICATIONS
- The four-step total synthesis of (−)-chaetominine
- (2013) Qi-Long Peng et al. CHEMICAL COMMUNICATIONS
- A novel and versatile method for the enantioselective syntheses of tropane alkaloids
- (2013) ZhongYi Mao et al. Science China-Chemistry
- Asymmetric formal total synthesis of the stemofoline alkaloids: the evolution, development, and application of a catalytic dipolar cycloaddition cascade
- (2013) Charles S. Shanahan et al. TETRAHEDRON
- An asymmetric synthesis of the pentacyclic core of stemofoline
- (2013) Thomas Burns et al. TETRAHEDRON LETTERS
- Enantioselective Formal Total Syntheses of Didehydrostemofoline and Isodidehydrostemofoline through a Catalytic Dipolar Cycloaddition Cascade
- (2012) Chao Fang et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Toward the Total Synthesis of Haliclonin A: Construction of a Tricyclic Substructure
- (2012) Shi-Peng Luo et al. CHEMISTRY-A EUROPEAN JOURNAL
- Total Synthesis of (±)-Parvineostemonine
- (2012) Zhi-Hua Chen et al. Chemistry-An Asian Journal
- Total Synthesis of (−)-Sessilifoliamide J
- (2012) Xue-Kui Liu et al. JOURNAL OF ORGANIC CHEMISTRY
- Enantioselective Total Syntheses of (−)-FR901483 and (+)-8-epi-FR901483
- (2012) Hao-Hua Huo et al. JOURNAL OF ORGANIC CHEMISTRY
- Flexible Approach to Stemona Alkaloids: Total Syntheses of (−)-Stemospironine and Three New Diastereoisomeric Analogs
- (2012) Nuria Bardají et al. ORGANIC LETTERS
- Synthesis of stemofoline analogues as acetylcholinesterase inhibitors
- (2012) Kwankamol Sastraruji et al. TETRAHEDRON
- Bioinspired and Concise Synthesis of (±)-Stemoamide
- (2011) Yan Wang et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Enantioselective Total Synthesis of (−)-Stenine
- (2011) Jingbo Chen et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Total Synthesis of (–)-Sessilifoliamide C and (–)-8-epi-Stemoamide
- (2011) Adam T. Hoye et al. ORGANIC LETTERS
- Development of the Intramolecular Prins Cyclization/Schmidt Reaction for the Construction of the Azaspiro[4,4]nonane: Application to the Formal Synthesis of (±)-Stemonamine
- (2011) Zhi-Hua Chen et al. ORGANIC LETTERS
- Oxidation of acyclic alkenes and allyl and benzyl ethers with DIB/t-BuOOH/Mg(OAc)2
- (2011) Thanapat Sastraruji et al. TETRAHEDRON
- Total synthesis of (±)-maistemonine and (±)-stemonamide
- (2010) Zhi-Hua Chen et al. CHEMICAL COMMUNICATIONS
- Semisynthesis and Acetylcholinesterase Inhibitory Activity of Stemofoline Alkaloids and Analogues
- (2010) Kwankamol Sastraruji et al. JOURNAL OF NATURAL PRODUCTS
- The chemistry of Stemona alkaloids: An update
- (2010) Ronaldo Aloise Pilli et al. NATURAL PRODUCT REPORTS
- Strategies for the Synthesis ofStemonaAlkaloids
- (2009) Ramon Alibés et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
- Semisynthesis and Biological Activity of Stemofoline Alkaloids
- (2009) Morwenna C. Baird et al. JOURNAL OF NATURAL PRODUCTS
- An approach to an asymmetric synthesis of stemofoline
- (2009) Eric J. Thomas et al. TETRAHEDRON-ASYMMETRY
- Application of an intramolecular dipolar cycloaddition to an asymmetric synthesis of the fully oxygenated tricyclic core of the stemofoline alkaloids
- (2008) Ryan J. Carra et al. TETRAHEDRON
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 NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started