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SPR Carbohydrate Chemistry
Carbohydrate Chemistry: Chemical and Biological Approaches, Volume 41
Edited by
Amelia Pilar Rauter;
Amelia Pilar Rauter
Universidade de Lisboa, Portugal
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Thisbe K. Lindhorst;
Thisbe K. Lindhorst
Kiel University, Germany
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Yves Queneau
Yves Queneau
INSA Lyon, France
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Volume
41
Hardback ISBN:
978-1-78262-121-8
PDF ISBN:
978-1-78262-060-0
EPUB ISBN:
978-1-78262-795-1
Special Collection:
2015 ebook collection
No. of Pages:
254
Publication date:
02 Dec 2015
Book Chapter
Pyranose glycals in the generation of skeletal diversity
By
Ana M. Gómez
;
Ana M. Gómez
Instituto de Química Orgánica General, IQOG-CSIC
Juan de la Cierva 3
28006 Madrid
Spain
ana.gomez@csic.esjc.lopez@csic.es
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Fernando Lobo
;
Fernando Lobo
Instituto de Química Orgánica General, IQOG-CSIC
Juan de la Cierva 3
28006 Madrid
Spain
ana.gomez@csic.esjc.lopez@csic.es
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J. Cristóbal López
J. Cristóbal López
Instituto de Química Orgánica General, IQOG-CSIC
Juan de la Cierva 3
28006 Madrid
Spain
ana.gomez@csic.esjc.lopez@csic.es
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Published:02 Dec 2015
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Special Collection: 2015 ebook collection
Citation
A. M. Gómez, F. Lobo, and J. C. López, in Carbohydrate Chemistry: Chemical and Biological Approaches, Volume 41, ed. A. Pilar Rauter, T. K. Lindhorst, and Y. Queneau, The Royal Society of Chemistry, 2015, vol. 41, pp. 26-58.
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The presence of an unsaturation in a pyranose derivative provides a powerful handle for the creation of new compounds displaying a variety of molecular skeletons. This contribution focuses on investigations related to the use of pyranose glycals in the creation of skeletally-diverse derivatives that have appeared in the literature during the last eight years.
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