A tandem reaction of organozinc reagent prepared from palladium-catalyzed umpolung method: diastereoselective formation of cyclohexene derivatives bearing three adjacent stereocenters
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2011/OB/C0OB00806K
Reference40 articles.
1. Recent advances in the use of tandem reactions for organic synthesis
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4. Tandem Diels−Alder Cycloadditions in Organic Synthesis
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1. Advances in tandem reactions with organozinc reagents;Chemical Society Reviews;2015
2. Design of Molecular Transformations Based on the Concerted Function of Two Zinc Atoms in Bis(iodozincio)methane;Synlett;2014-11-12
3. Diastereoselective synthesis of a highly functionalized cyclohexene embedded with a quaternary stereogenic centre by self Diels–Alder dimerization of a [3]dendralene attached to a (−)-menthol auxiliary;Tetrahedron: Asymmetry;2014-01
4. ChemInform Abstract: A Tandem Reaction of Organozinc Reagent Prepared from Palladium-Catalyzed Umpolung Method: Diastereoselective Formation of Cyclohexene Derivatives Bearing Three Adjacent Stereocenters.;ChemInform;2011-06-09
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