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Short And Efficient Synthesis Of Chiral Furyl Carbinols From Carbohydrates.

A. Boto, D. Hernández, R. Hernández
Published 2007 · Chemistry, Medicine

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[reaction: see text] Common sugar derivatives can be transformed in a few steps into chiral-substituted furyl carbinols. The mildness of the reaction conditions and the good yields obtained make this procedure an interesting alternative to the conventional processes.



This paper is referenced by
10.1016/J.TETASY.2010.02.004
Substituent effects on the stereochemical outcome of the baker’s yeast-mediated biotransformation of α-hydroxy- and α-acetoxymethyl-5-phenylfuran-2-yl-ethanones
L. Bencze (2010)
10.1021/ol4014574
Tandem Suzuki-Miyaura coupling/acid-catalyzed cyclization between vinyl ether boronates and vinyl halides: a concise approach to polysubstituted furans.
A. Butkevich (2013)
10.2174/1385272823666191122111351
Organo or Metal Complex Catalyzed Synthesis of Five-membered Oxygen Heterocycles
N. Kaur (2020)
10.1016/J.TETASY.2012.11.016
Lipase-catalyzed asymmetric acylation in the chemoenzymatic synthesis of furan-based alcohols
Piia Hara (2013)
10.1002/EJOC.201101274
One‐Pot Conversion of Serine Derivatives and Amino Sugars into Oxazine Derivatives of γ‐Aryl‐γ‐(hydroxy)amines
A. Boto (2012)
10.1021/acs.joc.7b00133
Synthesis of 2,5-Disubstituted Furans from Sc(OTf)3 Catalyzed Reaction of Aryl Oxiranediesters with γ-Hydroxyenones.
Keshab Mondal (2017)
10.1002/anie.201105795
An alkyne hydroacylation route to highly substituted furans.
Philip Lenden (2011)
10.1002/9783527634880.CH4
Furan and Its Derivatives
A. Boto (2011)
10.1002/EJOC.201000997
One-Pot Conversion of Proline Derivatives into Iodinated Iminosugar-Based Nucleosides, Useful Precursors of Highly Functionalized Nucleoside Analogues
A. Boto (2010)
10.1039/c4ob01372g
Metal-free, one-pot conversion of proline derivatives into 2-aryl-3-iodo pyrrolidines by a sequential scission-iodination-arylation process.
Venkateswara Rao Batchu (2014)
10.1002/EJOC.200900427
Coupling Radical and Ionic Processes: An Unusual Rearrangement Affords Sugar and C-Glycoside Derivatives
A. Boto (2009)
10.1039/c2ob25433f
Preparation of modified peptides: direct conversion of α-amino acids into β-amino aldehydes.
Carlos J Saavedra (2012)
10.1021/jo301031t
Stereoselective conversion of sugar derivatives into C-nucleosides.
J. Miguélez (2012)
10.1021/acs.joc.5b02500
Base Induced Chiral Substituted Furans and Imidazoles from Carbohydrate-Derived 2-Haloenones.
Kanchan Mal (2016)
10.1002/AJOC.201300219
Synthesis of the Aglycone of the Argelosides: Antiproliferative 14,15‐seco‐Pregnane Glycosides
M. Tamiya (2014)
10.1002/EJOC.201200162
Synthesis of Substituted Furans through Domino Aldol/Homo‐Michael Reactions of Formylcyclopropane 1,1‐Diesters with 1,3‐Dicarbonyls
Jilai Bao (2012)
10.1080/00397911.2018.1485165
Photochemical mediated reactions in five-membered O-heterocycles synthesis
N. Kaur (2018)
10.1002/9781118341155.CH3
Hypervalent Iodine Reagents in Organic Synthesis
V. V. Zhdankin (2013)
10.1016/J.TETLET.2010.06.031
Base-promoted selective β-fragmentation of homoallylamines
W. Li (2010)
10.1002/chem.201402286
Gold(III) chloride catalyzed synthesis of chiral substituted 3-formyl furans from carbohydrates: application in the synthesis of 1,5-dicarbonyl derivatives and furo[3,2-c]pyridine.
Kanchan Mal (2014)
10.1002/EJOC.201000360
One-Pot Synthesis of Azanucleosides from Proline Derivatives -Stereoselectivity in Sequential Processes
A. Boto (2010)
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