Chirality pairing recognition, a unique reaction forming spiral alkaloids from amino acids stereoselectively in one-pot-Reference-Cited by-同舟云学术

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Chirality pairing recognition, a unique reaction forming spiral alkaloids from amino acids stereoselectively in one-pot

Published:2012-03-07 Issue:2 Volume:2 Page:53-58
ISSN:2192-2195
Container-title:Natural Products and Bioprospecting
language:en
Short-container-title:Nat. Prod. Bioprospect.

Author:

Bai Bing,Li Da-Shan,Huang Sheng-Zhuo,Ren Jie,Zhu Hua-Jie

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Plant Science,Pharmacology,Toxicology,Biochemistry,Food Science,Analytical Chemistry

Link

http://link.springer.com/article/10.1007/s13659-012-0003-6/fulltext.html

Reference8 articles.

1. Rich, A. J. Biol. Chem.2006, 281, 7693–7696.

2. Forsdyke, D. R. J. Theo. Biology.2007, 249, 325–330.

3. Ikai, T.; Okamoto, Y. Chem. Rev.2009, 109, 6077–6101.

4. Bai, B.; Shen, L.; Ren, J.; Zhu, H. J. Adv. Syn. & Cat.2011, accepted. Doi:10.1002/adsc.201100592.

5. Bou-Hamdan, F. R.; Leighton, J. L. Angew. Chem. Int. Ed.2009, 48, 2403–2406.

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1. Synthesis of Constrained Peptidomimetics via the Pictet-Spengler Reaction;Topics in Heterocyclic Chemistry;2016

2. Chirality;Organic Stereochemistry;2015-06-26

3. Remote Amide-Controlled Gold-Catalyzed Stereoselective Hydro-heteroarylation of Acrylamides: Access to Pyrido[3,4-b]indoles;European Journal of Organic Chemistry;2015-02-25

4. Post-Ugi gold-catalyzed diastereoselective domino cyclization for the synthesis of diversely substituted spiroindolines;Beilstein Journal of Organic Chemistry;2013-10-14

5. A Diversity-Oriented Approach to Spiroindolines: Post-Ugi Gold-Catalyzed Diastereoselective Domino Cyclization;Angewandte Chemie International Edition;2012-08-21

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