Results 81 to 90 of about 18,239,073 (189)
Stereoselective intramolecular 1,3-dipolar cycloadditions
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
Intramolecular cycloadditions with high regio- and stereocontrol are important methods for the efficient assembly of complex molecular structures. Efficient routes to the synthesis of norbornadiene-tethered nitrile oxides have been developed, and their ...
Robert Jordan (346146) +3 more
core +2 more sources
Transition metal catalyzed 1-3-dipolar cycloaddition of carbethoxycarbene to acrylonitrile [PDF]
Paulissen, R. +3 more
openaire +2 more sources
1, 3-Dipolar Cycloaddition of Nitrones to Enamines
Otohiko TSUGE +2 more
openaire +2 more sources
1, 3-Dipolar Cycloaddition Reaction of Aziridinedicarboximide
OIDA, SADAO, OHKI, EIJI
openaire +2 more sources
Although metal-free cycloadditions of cyclooctynes and azides to give stable 1,2,3-triazoles have found wide utility in chemical biology and material sciences, there is an urgent need for faster and more versatile bioorthogonal reactions.
Brian C. Sanders (2234539) +8 more
core +1 more source
The major purpose of the research is the development of novel catalytic reactions for regio- and stereodivergent cycloadditions to construct heterocyclic moieties. Three different types of divergent catalytic reactions have been investigated.
전현지
core +1 more source
Bipyrazolidin-3-one derivatives are biologically significant compounds and their importance has increased in the past decades. In this paper, the first stereoselective [3 + 2] dipolar cycloadditions of azomethine imines with alpha,beta-unsaturated ...
Du, W +7 more
core
Catalytic [6 + 3] cycloaddition for the synthesis of medium-sized ring systems: a critical review. [PDF]
Archna +4 more
europepmc +1 more source
Highly Stereoselective (3+2) Cycloadditions of Levoglucosenone (LGO) with the In Situ-Generated Thiocarbonyl <i>S</i>-Methanides (Thiocarbonyl Ylides) Derived from Aromatic and Cycloaliphatic Thioketones. [PDF]
Mlostoń G +4 more
europepmc +1 more source

