Asymmetric Total Synthesis and Absolute Configuration Reassignment of Indole Alkaloid (+)-Alsmaphorazine D

2016 ◽  
Vol 74 (5) ◽  
pp. 410 ◽  
Author(s):  
Kuan Yu ◽  
Beiling Gao ◽  
Hanfeng Ding
Keyword(s):  
Total Synthesis ◽  
Absolute Configuration ◽  
Indole Alkaloid ◽  
Asymmetric Total Synthesis

Determination of absolute configuration of trimeric indole alkaloid, psychotrimine, by first asymmetric total synthesis

2010 ◽  
Vol 46 (14) ◽  
pp. 2501 ◽  
Author(s):  
Nobuaki Takahashi ◽  
Takeshi Ito ◽  
Yohei Matsuda ◽  
Noriyuki Kogure ◽  
Mariko Kitajima ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Absolute Configuration ◽  
Indole Alkaloid ◽  
Asymmetric Total Synthesis ◽  
Determination Of Absolute Configuration

ChemInform Abstract: Determination of Absolute Configuration of Trimeric Indole Alkaloid, Psychotrimine, by First Asymmetric Total Synthesis.

ChemInform ◽  
2010 ◽  
Vol 41 (32) ◽  
pp. no-no
Author(s):  
Nobuaki Takahashi ◽  
Takeshi Ito ◽  
Yohei Matsuda ◽  
Noriyuki Kogure ◽  
Mariko Kitajima ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Absolute Configuration ◽  
Indole Alkaloid ◽  
Asymmetric Total Synthesis ◽  
Determination Of Absolute Configuration

Asymmetric Total Synthesis of Pentacyclic Indole Alkaloid Andranginine and Absolute Configuration of Natural Product Isolated from Kopsia arborea

2017 ◽  
Vol 19 (10) ◽  
pp. 2722-2725 ◽  
Author(s):  
Shino Tooriyama ◽  
Yuji Mimori ◽  
Yuqiu Wu ◽  
Noriyuki Kogure ◽  
Mariko Kitajima ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Natural Product ◽  
Absolute Configuration ◽  
Indole Alkaloid ◽  
Asymmetric Total Synthesis

Asymmetric Total Synthesis and Determination of the Absolute Configuration of (+)-Srilankenyne via Sequence-Sensitive Halogenations Guided by Conformational Analysis

2021 ◽  
Vol 23 (4) ◽  
pp. 1321-1326
Author(s):  
Hongjun Jang ◽  
Soo Yeon Kwak ◽  
Dongjoo Lee ◽  
Juan V. Alegre-Requena ◽  
Hyoungsu Kim ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Conformational Analysis ◽  
Absolute Configuration ◽  
Asymmetric Total Synthesis ◽  
The Absolute

Asymmetric Total Synthesis of 16-Methyleicos-(4E )-en-1-yn-3-ol from the Marine Sponge Cribrochalina vasculum : Establishment of Absolute Configuration of Chiral Centers

2019 ◽  
Vol 4 (1) ◽  
pp. 399-402 ◽  
Author(s):  
Narayana Rao Gundoju ◽  
Ramesh Bokam ◽  
Nageswara Rao Yalavarthi ◽  
Karimulla Shaik ◽  
Mangala Gowri Ponnapalli
Keyword(s):  
Total Synthesis ◽  
Absolute Configuration ◽  
Marine Sponge ◽  
Asymmetric Total Synthesis ◽  
Chiral Centers

Asymmetric Total Synthesis and Absolute Configuration Determination of (−)-Verrupyrroloindoline

2018 ◽  
Vol 20 (14) ◽  
pp. 4200-4203 ◽  
Author(s):  
Zhi-Ping Yang ◽  
Qian He ◽  
Jian-Liang Ye ◽  
Pei-Qiang Huang
Keyword(s):  
Total Synthesis ◽  
Absolute Configuration ◽  
Asymmetric Total Synthesis

Total Synthesis of (–)-Alstofolinine A: Selected Furan Oxidation/ Cyclization Cascade

Synlett ◽  
2019 ◽  
Vol 31 (01) ◽  
pp. 7-12 ◽  
Author(s):  
Ye Zhang ◽  
Lei Zhang ◽  
Xiangbing Qi
Keyword(s):  
Total Synthesis ◽  
Common Core ◽  
Nucleophilic Addition ◽  
Addition Reaction ◽  
Indole Alkaloids ◽  
Indole Alkaloid ◽  
Asymmetric Total Synthesis ◽  
Ring Systems ◽  
Synthetic Strategy ◽  
Nucleophilic Addition Reaction

Indole-fused tetracyclic ring systems containing nitrogen atoms are common core skeletons of many indole alkaloids such as sarpagine, macroline, and ajmaline. Efficient and stereoselective construction of these ring systems can promote the development of the corresponding alkaloid syntheses. In this article, we briefly summarize our current progress toward the application of the aza-Achmatowicz reaction and indole nucleophilic addition reaction cascade for the first asymmetric total synthesis of the macroline-type indole alkaloid (–)-Alstofolinine A. Our synthetic strategy is based on furan oxidation/rearrangement and proceeds from easily accessible materials such as indole and furan derivatives.

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