Results 81 to 90 of about 4,239 (193)

Stereoselective intramolecular 1,3-dipolar cycloadditions

open access: yes, 2001
An in depth account of intramolecular 1,3-dipolar cycloadditions involving dipoles such as nitrile oxides, silyl nitronates, H-nitrones, azides, and nitrilimines is presented with particular emphasis on the stereochemistry during the cyclo addition ...
HASSNER, A, NAMBOOTHIRI, INN
core  

Lewis Acid-Catalyzed Enantioselective 1,3-Dipolar Cycloadditions of Diazoalkane:  Chiral Ligand/Achiral Auxiliary Cooperative Chirality Control

open access: yes, 2016
Lewis Acid-Catalyzed Enantioselective 1,3-Dipolar Cycloadditions of Diazoalkane:  Chiral Ligand/Achiral Auxiliary Cooperative Chirality ...
Shuji Kanemasa (2513860)   +1 more
core   +1 more source

An Overlooked Pathway in 1,3-Dipolar Cycloadditions of Diazoalkanes with Enamines. [PDF]

open access: yesAngew Chem Int Ed Engl, 2022
Li L   +5 more
europepmc   +1 more source

1,3-dipolar cycloaddition reactions of C-60 with 3-phenyl-phthalazinium-1-olate. A theoretical study

open access: yes, 2002
1,3-Dipolar cycloaddition products of the reaction between C-60 and 1-phenyl-phthalazinium-1-olate were studied within the framework of AM1(RHF) level. The reactions involving the double bond between two hexagons and a hexagon and a pentagon, as well as ...
Türker, Burhan Lemi
core  

1,3-Dipolar cycloadditions: applications to the synthesis of antiviral agents

open access: yes, 2009
In the present perspective the advances and real possibilities of 1,3-dipolar cycloadditions as key steps in the total synthesis of virus inhibitors are described.
Nájera, Carmen, Sansano, Jose M.
core   +1 more source

Electrocyclic Ring‐Opening of 1,2,4‐Oxadiazole[4,5‐a]piridinium Chloride: a New Route to 1,2,4‐Oxadiazole Dienamino Compounds

open access: yesChemistryOpen, 2019
1,2,4‐Oxadiazole[4,5‐a]piridinium chloride adds nucleophiles to undergo electrocyclic ring opening affording 1,2,4‐oxadiazole dienamino derivatives. These pyridinium salts represent a special class of Zincke salts that are prone to rearrange when treated
Dr. Stefano Carella   +2 more
doaj   +1 more source

A Novel Cycloaddition Reaction of Thermally Generated Sulfenes

open access: yesCHIMIA, 1992
The highly strained ?-sultine 4, resulting from the addition of SO2 to benzobenzvalene, is shown to undergo a thermal cycloreversion which gives 1H-indene-1-thiocarbaldehyde dioxide (6) as an intermediate and subsequently 1H-indene-1 ...
Ulrich Burger   +3 more
doaj   +2 more sources

Acceleration of 1,3-Dipolar Cycloadditions by Integration of Strain and Electronic Tuning. [PDF]

open access: yesJ Am Chem Soc, 2021
Dones JM   +4 more
europepmc   +1 more source

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