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A simple route for renewable nano-sized arjunolic and asiatic acids and self-assembly of arjuna-bromolactone

While separating two natural nano-sized triterpenic acids via bromolactonization, we serendipitously discovered that arjuna-bromolactone is an excellent gelator of various organic solvents. A simple and efficient method for the separation of two triterpenic acids and the gelation ability and solid s...

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Autores principales: Bag, Braja G, Dey, Partha P, Dinda, Shaishab K, Sheldrick, William S, Oppel, Iris M
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2511022/
https://www.ncbi.nlm.nih.gov/pubmed/18941493
http://dx.doi.org/10.3762/bjoc.4.24
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author Bag, Braja G
Dey, Partha P
Dinda, Shaishab K
Sheldrick, William S
Oppel, Iris M
author_facet Bag, Braja G
Dey, Partha P
Dinda, Shaishab K
Sheldrick, William S
Oppel, Iris M
author_sort Bag, Braja G
collection PubMed
description While separating two natural nano-sized triterpenic acids via bromolactonization, we serendipitously discovered that arjuna-bromolactone is an excellent gelator of various organic solvents. A simple and efficient method for the separation of two triterpenic acids and the gelation ability and solid state 1D-helical self-assembly of nano-sized arjuna-bromolactone are reported.
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spelling pubmed-25110222008-10-20 A simple route for renewable nano-sized arjunolic and asiatic acids and self-assembly of arjuna-bromolactone Bag, Braja G Dey, Partha P Dinda, Shaishab K Sheldrick, William S Oppel, Iris M Beilstein J Org Chem Preliminary Communication While separating two natural nano-sized triterpenic acids via bromolactonization, we serendipitously discovered that arjuna-bromolactone is an excellent gelator of various organic solvents. A simple and efficient method for the separation of two triterpenic acids and the gelation ability and solid state 1D-helical self-assembly of nano-sized arjuna-bromolactone are reported. Beilstein-Institut 2008-07-09 /pmc/articles/PMC2511022/ /pubmed/18941493 http://dx.doi.org/10.3762/bjoc.4.24 Text en Copyright © 2008, Bag et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Preliminary Communication
Bag, Braja G
Dey, Partha P
Dinda, Shaishab K
Sheldrick, William S
Oppel, Iris M
A simple route for renewable nano-sized arjunolic and asiatic acids and self-assembly of arjuna-bromolactone
title A simple route for renewable nano-sized arjunolic and asiatic acids and self-assembly of arjuna-bromolactone
title_full A simple route for renewable nano-sized arjunolic and asiatic acids and self-assembly of arjuna-bromolactone
title_fullStr A simple route for renewable nano-sized arjunolic and asiatic acids and self-assembly of arjuna-bromolactone
title_full_unstemmed A simple route for renewable nano-sized arjunolic and asiatic acids and self-assembly of arjuna-bromolactone
title_short A simple route for renewable nano-sized arjunolic and asiatic acids and self-assembly of arjuna-bromolactone
title_sort simple route for renewable nano-sized arjunolic and asiatic acids and self-assembly of arjuna-bromolactone
topic Preliminary Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2511022/
https://www.ncbi.nlm.nih.gov/pubmed/18941493
http://dx.doi.org/10.3762/bjoc.4.24
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