Synthesis of tetrasubstituted 1-silyloxy-3-aminobutadienes and chemistry beyond Diels–Alder reactions-Reference-Cited by-同舟云学术

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Synthesis of tetrasubstituted 1-silyloxy-3-aminobutadienes and chemistry beyond Diels–Alder reactions

Published:2015-04-21 Issue:1 Volume:6 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Li Xijian,Peng Siyu,Li Li,Huang Yong

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/ncomms7913.pdf

Reference39 articles.

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2. Kozmin, S. A., Iwama, T., Huang, Y. & Rawal, V. H. An efficient approach to aspidosperma alkaloids via [4+2] cycloadditions of aminosiloxydienes: Stereocontrolled total synthesis of (±)-Tabersonine. Gram-scale catalytic asymmetric syntheses of (+)-Tabersonine and (+)-16-Methoxytabersonine. Asymmetric syntheses of (+)-Aspidospermidine and (−)-Quebrachamine. J. Am. Chem. Soc. 124, 4628–4641 (2002).

3. Smith, A. B. III, Basu, K. & Bosanac, T. Total synthesis of (−)-Okilactomycin. J. Am. Chem. Soc. 129, 14872–14874 (2007).

4. Hayashida, J. & Rawal, V. H. Total synthesis of (±)-Platencin. Angew. Chem. Int. Ed. 47, 4373–4376 (2008).

5. You, L.-F. et al. An enantioselective synthesis of the ABD tricycle for (−)-Phomactin A featuring Rawal’s asymmetric Diels–Alder cycloaddition. Adv. Synth. Catal. 350, 2885–2891 (2008).

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