Full Paper View Go Back
Resolution of 2-Hydroxypropanoic Acid by using Chiral Auxiliary
Yogesh Jayntibhai Sanghani1 , Krushna Kumar Jethalal Jilariya2
- School of science, Research Scholar, R.K. University, Rajkot, India.
- Department of chemistry, Research Scholar, Saurashtra University, Rajkot, India.
Correspondence should be addressed to: yogeshsanghani4027@yahoo.com.
Section:Research Paper, Product Type: Isroset-Journal
Vol.4 ,
Issue.6 , pp.9-12, Dec-2017
CrossRef-DOI: https://doi.org/10.26438/ijsrcs/v4i6.912
Online published on Dec 31, 2017
Copyright © Yogesh Jayntibhai Sanghani, Krushna Kumar Jethalal Jilariya . This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
View this paper at Google Scholar | DPI Digital Library
How to Cite this Paper
- IEEE Citation
- MLA Citation
- APA Citation
- BibTex Citation
- RIS Citation
IEEE Style Citation: Yogesh Jayntibhai Sanghani, Krushna Kumar Jethalal Jilariya, “Resolution of 2-Hydroxypropanoic Acid by using Chiral Auxiliary,” International Journal of Scientific Research in Chemical Sciences, Vol.4, Issue.6, pp.9-12, 2017.
MLA Style Citation: Yogesh Jayntibhai Sanghani, Krushna Kumar Jethalal Jilariya "Resolution of 2-Hydroxypropanoic Acid by using Chiral Auxiliary." International Journal of Scientific Research in Chemical Sciences 4.6 (2017): 9-12.
APA Style Citation: Yogesh Jayntibhai Sanghani, Krushna Kumar Jethalal Jilariya, (2017). Resolution of 2-Hydroxypropanoic Acid by using Chiral Auxiliary. International Journal of Scientific Research in Chemical Sciences, 4(6), 9-12.
BibTex Style Citation:
@article{Sanghani_2017,
author = {Yogesh Jayntibhai Sanghani, Krushna Kumar Jethalal Jilariya},
title = {Resolution of 2-Hydroxypropanoic Acid by using Chiral Auxiliary},
journal = {International Journal of Scientific Research in Chemical Sciences},
issue_date = {12 2017},
volume = {4},
Issue = {6},
month = {12},
year = {2017},
issn = {2347-2693},
pages = {9-12},
url = {https://www.isroset.org/journal/IJSRCS/full_paper_view.php?paper_id=498},
doi = {https://doi.org/10.26438/ijcse/v4i6.912}
publisher = {IJCSE, Indore, INDIA},
}
RIS Style Citation:
TY - JOUR
DO = {https://doi.org/10.26438/ijcse/v4i6.912}
UR - https://www.isroset.org/journal/IJSRCS/full_paper_view.php?paper_id=498
TI - Resolution of 2-Hydroxypropanoic Acid by using Chiral Auxiliary
T2 - International Journal of Scientific Research in Chemical Sciences
AU - Yogesh Jayntibhai Sanghani, Krushna Kumar Jethalal Jilariya
PY - 2017
DA - 2017/12/31
PB - IJCSE, Indore, INDIA
SP - 9-12
IS - 6
VL - 4
SN - 2347-2693
ER -
Abstract :
Chiral auxiliary molecule is used as consideration interacting with intermolecular interactions and different enantiomer intermediates. Partition of racemic mixture exploitation chiral auxiliary the primary reaction of enantiomers with chiral auxiliary to formation of diastereomers Diastereomers has completely dissimilar properties therefore it`s merely separated by posture or crystallization. Partition of Enantiomers useful an essential industrial and sustainable issue. Synthesis of desymmetrization and lots of partition may be a crucial methodology for the desymmetrization of the racemic mixture.
Key-Words / Index Term :
Enantiomer,Chiralauxiliary,Distereomers,Recemicmixtures
References :
[1] Dorgan, J. R., Lehermeier, H., Mang, M., “Thermal and physics properties of commercial-grade poly (lactic acid) s”, J.Polym. Eviron., 8, 1-9, 2000.
[2] Sauer, M., Porro, D., Mattanovich, D., Branduardi, P., “Microbial production of organic acids: increasing the markets”, TrendsBiotechnol., 26, 100-108, 2008.
[3] Nagasawa, N., Ayako, A., Kanazawa, S., Yagi, T., Mitomo, H.,
Yoshii, F., Tamada, M., “Application of poly(lactic acid) changed by radiation crosslinking”, Nucl. Instr. Meth. Phys. Res. B, 236, 611-616, 2005.
[4] Okamoto, K., Toshima K., Matsumura, S., “Degradation of poly(lactic acid) into polymerizable oligomer exploitation montmorillonite K10 for chemical recycling”, Macromol. Biosci., 5, 813-820, 2005.
[5] Tsukegi, T., Motoyama, T., Shirai, Y., Nishida, H., Endo, T.,
“Racemization behaviour of L,L-lactide throughout heating”, Polym.Degrad. Stab., 92, 552-559, 2007.
[6] Motoyama, T., Tsukegi, T., Shitai, Y., Nishida, H., Endo, T.,
“Effects of MgO catalyst on depolymerization of poly-L-2-hydroxypropanoic acid to L,L-lactide”, Polym. Degrad. Stab., 92, 1350-1358, 2007.
[7] Tsuji, H., Ikada, Y., “Stereocomplex formation between enantiomeric poly (lactic acid)s. XI. Mechanical properties and morphology of solution-cast films”, Polymer, 40, 6699-6708, 1999.
[8] Lunt, J., “Large-scale production, properties and business applications of poly2-hydroxypropanoic acid polymers”, Polym. Degrad. Stab., 59, 145-152, 1998.
[9]Yang, F., Murugan, R., Wang, S., Ramakrishna, S.,
“Electrospinning of nano/micro scale poly(L-lactic acid) aligned fibers and their potential in neural tissue engineering”,Biomaterials, 26, 2603-2610, 2005.
You do not have rights to view the full text article.
Please contact administration for subscription to Journal or individual article.
Mail us at support@isroset.org or view contact page for more details.