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- The sorbicillinoid family of natural products: Isolation, biosynthesis, and synthetic studies. Andrew M. Harned, Kelly A. Volp
, Nat. Prod. Rep.
, 2011
, 28
, 1790
- Structural elucidation of trichotetronines: polyketides possessing a bicyclo[2.2.2]octane skeleton with a tetronic acid moiety isolated from Trichoderma sp.. Osamu Shirota, Vibha Pathak, Chowdhury Faiz Hossain, Setsuko Sekita, Kosuke Takatori, Motoyoshi Satake
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 2961
- Tandem reactions, cascade sequences, and biomimetic strategies in total synthesis. K. C. Nicolaou, Tamsyn Montagnon, Scott A. Snyder
, Chem. Commun.
, 2003
, 551
- Synthetic approaches to oligomeric natural products. Scott A. Snyder, Adel M. ElSohly, Ferenc Kontes
, Nat. Prod. Rep.
, 2011
, 28
, 897
- Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance. K. C. Nicolaou, Christopher R. H. Hale, Christian Nilewski, Heraklidia A. Ioannidou
, Chem. Soc. Rev.
, 2012
, 41
, 5185
- “Common synthetic scaffolds” in the synthesis of structurally diverse natural products. Elissavet E. Anagnostaki, Alexandros L. Zografos
, Chem. Soc. Rev.
, 2012
, 41
, 5613
- The biosynthesis of bisvertinolone: evidence for oxosorbicillinol as a direct precursor. Naoki Abe, Tadaharu Arakawa, Akira Hirota
, Chem. Commun.
, 2002
, 204
- Dearomative logic in natural product total synthesis. Christopher J. Huck, Yaroslav D. Boyko, David Sarlah
, Nat. Prod. Rep.
, 2022
, 39
, 2231
- An enantioselective cascade for simultaneous generation of five quaternary stereocenters from fully substituted enones. Shu-Mei Yang, Ganapuram Madhusudhan Reddy, Tzu-Ping Wang, Yu-Sheng Yeh, Min Wang, Wenwei Lin
, Chem. Commun.
, 2017
, 53
, 7649
- Professor K. C. Nicolaou*
. K.C. Nicolaou
, J. Chem. Soc., Perkin Trans. 1
, 2002
, 5-vii