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

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

Asymmetric Total Synthesis of (+)-K01-0509 B:  Determination of Absolute Configuration

2006 ◽  
Vol 8 (24) ◽  
pp. 5577-5580 ◽  
Author(s):  
Satoshi Tsuchiya ◽  
Toshiaki Sunazuka ◽  
Tomoyasu Hirose ◽  
Ryuma Mori ◽  
Toshiaki Tanaka ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Absolute Configuration ◽  
Asymmetric Total Synthesis ◽  
Determination Of Absolute Configuration

scholarly journals Asymmetric Total Synthesis of (+)-K01-0509 B: Determination of Absolute Configuration.

ChemInform ◽  
2007 ◽  
Vol 38 (14) ◽  
Author(s):  
Satoshi Tsuchiya ◽  
Toshiaki Sunazuka ◽  
Tomoyasu Hirose ◽  
Ryuma Mori ◽  
Toshiaki Tanaka ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Absolute Configuration ◽  
Asymmetric Total Synthesis ◽  
Determination Of Absolute Configuration

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

(-)-Strempeliopine, stereoselective total synthesis and the determination of absolute configuration

1986 ◽  
Vol 51 (8) ◽  
pp. 1731-1742 ◽  
Author(s):  
Josef Hájíček ◽  
Jan Trojánek
Keyword(s):  
Circular Dichroism ◽  
Total Synthesis ◽  
Absolute Configuration ◽  
Determination Of Absolute Configuration ◽  
Natural Base ◽  
The Absolute ◽  
Circular Dichroïsm

A synthesis of (±)-strempeliopine (II) is described, the key step of which is the stereoselective reductive rearrangement of 18-methylene-1,2-dehydroaspidospermidine (XI). The absolute configuration of the natural (-)-base II was determined as (2S, 7R, 20R, 21R) on the basis of its synthesis from (+)-18-methylenevincadifformine (XVII) the configuration of which was derived from a comparison of circular dichroism properties of bases with a β-anilinoacrylate chromophore. The biogenesis of the alkaloids of the schizozygane type is discussed.

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
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