ChemInform Abstract: Total Synthesis and Absolute Stereochemistry of (+)-Batzellaside B (I) and Its C8-Epimer, a New Class of Piperidine Alkaloids from the Sponge Batzella sp.

ChemInform ◽  
2011 ◽  
Vol 42 (23) ◽  
pp. no-no
Author(s):  
Jolanta Wierzejska ◽  
Manami Ohshima ◽  
Toshiyasu Inuzuka ◽  
Tetsuya Sengoku ◽  
Masaki Takahashi ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Piperidine Alkaloids ◽  
New Class ◽  
Absolute Stereochemistry

scholarly journals Total synthesis and absolute stereochemistry of (+)-batzellaside B and its C8-epimer, a new class of piperidine alkaloids from the sponge Batzella sp.

2011 ◽  
Vol 52 (11) ◽  
pp. 1173-1175 ◽  
Author(s):  
Jolanta Wierzejska ◽  
Manami Ohshima ◽  
Toshiyasu Inuzuka ◽  
Tetsuya Sengoku ◽  
Masaki Takahashi ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Piperidine Alkaloids ◽  
New Class ◽  
Absolute Stereochemistry

ChemInform Abstract: The First Total Synthesis of N1999-A2: Absolute Stereochemistry and Stereochemical Implications into DNA Cleavage.

ChemInform ◽  
2010 ◽  
Vol 33 (14) ◽  
pp. no-no
Author(s):  
Shoji Kobayashi ◽  
Shukuko Ashizawa ◽  
Yusuke Takahashi ◽  
Yukio Sugiura ◽  
Makoto Nagaoka ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Dna Cleavage ◽  
Absolute Stereochemistry

Recent Advances in the Total Synthesis of Clavaminols

Synthesis ◽  
2018 ◽  
Vol 50 (23) ◽  
pp. 4569-4576
Author(s):  
Tian Jin ◽  
Lu Zhao ◽  
Zhe-Bin Zheng ◽  
Xiao Liu ◽  
Liang Sun ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Research Groups ◽  
Total Syntheses ◽  
New Class ◽  
Recent Advances ◽  
Molecular Architectures ◽  
Synthetic Approaches ◽  
Long Chain

Clavaminols are a new class of long-chain 2-amino-3-­alkanols that mostly contain 2R,3S-configurations. Owing to their interesting molecular architectures and promising activities, they have ­become popular targets for synthetic organic chemists. In this review, we highlight 12 total syntheses of clavaminols from different research groups during the period 2009 to 2018.1 Introduction2 Synthetic Approaches toward Clavaminols2.1 Total Synthesis by Chemla and Colleagues (2009)2.2 Total Synthesis by Greck and Colleagues (2010)2.3 Total Synthesis by Sutherland and Zaed (2011)2.4 Total Synthesis by Huang and Colleagues (2011)2.5 Total Synthesis by Kotora and Colleagues (2012)2.6 Total Synthesis by Kumar and Colleagues (2013)2.7 Total Synthesis by Prabhavathi Devi and Colleagues (2013 and 2016)2.8 Total Synthesis by Sarabia and Colleagues (2014)2.9 Total Synthesis by Mohapatra and Colleagues (2016)2.10 Total Synthesis by Lu and Colleagues (2016)2.11 Total Synthesis by Jin and Colleagues (2017)2.12 Total Synthesis by Kumar Pandey and Colleagues (2018)3 Conclusion

Sign in / Sign up

Export Citation Format

Share Document