Results 291 to 300 of about 40,506 (345)
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Journal of Organic Chemistry, 2017
A synthetic procedure to access 2-unsubstituted pyrrolidines and piperidines is presented. In the presence of MgI2 as Lewis acid, donor-acceptor cyclopropanes or corresponding cyclobutanes were treated with 1,3,5-triazinanes, leading to the five- or six ...
L. K. B. Garve+3 more
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A synthetic procedure to access 2-unsubstituted pyrrolidines and piperidines is presented. In the presence of MgI2 as Lewis acid, donor-acceptor cyclopropanes or corresponding cyclobutanes were treated with 1,3,5-triazinanes, leading to the five- or six ...
L. K. B. Garve+3 more
semanticscholar +1 more source
2-cyano Δ3 piperidines IV: Spiroannelation in the piperidine series
Tetrahedron Letters, 1981Abstract The preparation of piperidines 7 and 11 spirosubstituted at C-2 from the 2-cyano Δ3 piperidine 5 is described. The mechanism of their formation is discussed.
H. Harris+2 more
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ChemInform Abstract: Stereoselective Synthesis of Piperidines
ChemInform, 2000AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Sabine Laschat, Tim Dickner
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Journal of the American Chemical Society, 2016
We have developed a novel approach for the synthesis of enantioenriched 3-boryl-tetrahydropyridines via the Cu(I)-catalyzed regio-, diastereo-, and enantioselective protoborylation of 1,2-dihydropyridines, which were obtained by the partial reduction of ...
K. Kubota+3 more
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We have developed a novel approach for the synthesis of enantioenriched 3-boryl-tetrahydropyridines via the Cu(I)-catalyzed regio-, diastereo-, and enantioselective protoborylation of 1,2-dihydropyridines, which were obtained by the partial reduction of ...
K. Kubota+3 more
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Organic Letters, 2016
The preparation of 2,6-substituted piperidine derivatives through diastereoselective C-H functionalization of corresponding nitrogen heterocycles represents an appealing protocol and yet remains a formidable challenge.
G. Wang, Ying Mao, Lei Liu
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The preparation of 2,6-substituted piperidine derivatives through diastereoselective C-H functionalization of corresponding nitrogen heterocycles represents an appealing protocol and yet remains a formidable challenge.
G. Wang, Ying Mao, Lei Liu
semanticscholar +1 more source
Organic and biomolecular chemistry, 2016
Utilizing molecular conformation as a controlling factor, epoxide-containing 2-aryl-piperidines can be ring-opened with the reagent combination of tetrabutylammonium fluoride (TBAF) and potassium bifluoride (KHF2) in a regioselective and divergent ...
Nannan Yan+4 more
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Utilizing molecular conformation as a controlling factor, epoxide-containing 2-aryl-piperidines can be ring-opened with the reagent combination of tetrabutylammonium fluoride (TBAF) and potassium bifluoride (KHF2) in a regioselective and divergent ...
Nannan Yan+4 more
semanticscholar +1 more source
Organic Letters, 2015
A new rhodium-catalyzed asymmetric arylative cyclization of nitrogen-tethered alkyne-enoate with arylboronic acids is described. In this process two new carbon-carbon bonds and one stereocenter are formed, providing access to pyrrolidines and piperidines
Fabien Serpier+4 more
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A new rhodium-catalyzed asymmetric arylative cyclization of nitrogen-tethered alkyne-enoate with arylboronic acids is described. In this process two new carbon-carbon bonds and one stereocenter are formed, providing access to pyrrolidines and piperidines
Fabien Serpier+4 more
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The chemistry of piperidines—I
Tetrahedron, 1973Abstract The reaction of pyrrolidine, piperidine and morpholine enamines of 1-methyl-4-piperidone with acraldehyde is found to be a convenient route to 3-aza-3-methyl-6-cycloalkylaminobicyclo[3.3.1]-nonan-9-ones. In each case two difficultly separable ketones are obtained which on reduction give mixtures of isomeric alcohols.
A.Z. Britten, J. O'Sullivan
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Immobilization of a Photoswitchable Piperidine Base
Organic Letters, 2009The synthesis of a photoswitchable piperidine base, carrying a monochlorosilane anchoring group, and its immobilization on silica gel, mimicking an oxide surface, is reported. Efficient photoswitching between the E and Z isomers of the azobenzene photochrome was demonstrated for the immobilization precursor in solution and the immobilized piperidine ...
Stefan Hecht, Ragnar S. Stoll
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Organic Letters, 2015
A new addition-carbocyclization cascade reaction initiated by arylboronic acids and catalyzed by a rhodium/chiral diene complex is described. Starting from N-bridged oxoenoate derivatives, highly functionalized piperidines bearing three contiguous ...
Fabien Serpier+3 more
semanticscholar +1 more source
A new addition-carbocyclization cascade reaction initiated by arylboronic acids and catalyzed by a rhodium/chiral diene complex is described. Starting from N-bridged oxoenoate derivatives, highly functionalized piperidines bearing three contiguous ...
Fabien Serpier+3 more
semanticscholar +1 more source