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

A novel chirality pairing recognition was found between D- and L-amino acid derivatives. Novel spiral alkaloids formed in the recognition reaction. Possible mechanism was proposed for the stereoselective and chemoselective reactions. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary...

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Detalles Bibliográficos
Autores principales: Bai, Bing, Li, Da-Shan, Huang, Sheng-Zhuo, Ren, Jie, Zhu, Hua-Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2012
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131586/
http://dx.doi.org/10.1007/s13659-012-0003-6
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author Bai, Bing
Li, Da-Shan
Huang, Sheng-Zhuo
Ren, Jie
Zhu, Hua-Jie
author_facet Bai, Bing
Li, Da-Shan
Huang, Sheng-Zhuo
Ren, Jie
Zhu, Hua-Jie
author_sort Bai, Bing
collection PubMed
description A novel chirality pairing recognition was found between D- and L-amino acid derivatives. Novel spiral alkaloids formed in the recognition reaction. Possible mechanism was proposed for the stereoselective and chemoselective reactions. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s13659-012-0003-6 and is accessible for authorized users.
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spelling pubmed-41315862014-08-20 Chirality pairing recognition, a unique reaction forming spiral alkaloids from amino acids stereoselectively in one-pot Bai, Bing Li, Da-Shan Huang, Sheng-Zhuo Ren, Jie Zhu, Hua-Jie Nat Prod Bioprospect Regular Article A novel chirality pairing recognition was found between D- and L-amino acid derivatives. Novel spiral alkaloids formed in the recognition reaction. Possible mechanism was proposed for the stereoselective and chemoselective reactions. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s13659-012-0003-6 and is accessible for authorized users. Springer Berlin Heidelberg 2012-03-07 /pmc/articles/PMC4131586/ http://dx.doi.org/10.1007/s13659-012-0003-6 Text en © The Author(s) 2012
spellingShingle Regular Article
Bai, Bing
Li, Da-Shan
Huang, Sheng-Zhuo
Ren, Jie
Zhu, Hua-Jie
Chirality pairing recognition, a unique reaction forming spiral alkaloids from amino acids stereoselectively in one-pot
title Chirality pairing recognition, a unique reaction forming spiral alkaloids from amino acids stereoselectively in one-pot
title_full Chirality pairing recognition, a unique reaction forming spiral alkaloids from amino acids stereoselectively in one-pot
title_fullStr Chirality pairing recognition, a unique reaction forming spiral alkaloids from amino acids stereoselectively in one-pot
title_full_unstemmed Chirality pairing recognition, a unique reaction forming spiral alkaloids from amino acids stereoselectively in one-pot
title_short Chirality pairing recognition, a unique reaction forming spiral alkaloids from amino acids stereoselectively in one-pot
title_sort chirality pairing recognition, a unique reaction forming spiral alkaloids from amino acids stereoselectively in one-pot
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131586/
http://dx.doi.org/10.1007/s13659-012-0003-6
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AT huangshengzhuo chiralitypairingrecognitionauniquereactionformingspiralalkaloidsfromaminoacidsstereoselectivelyinonepot
AT renjie chiralitypairingrecognitionauniquereactionformingspiralalkaloidsfromaminoacidsstereoselectivelyinonepot
AT zhuhuajie chiralitypairingrecognitionauniquereactionformingspiralalkaloidsfromaminoacidsstereoselectivelyinonepot

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