International audienceHerein we report regioselective deprotonations of 3- and 4-(tetrahydropyran-2-yloxy)pyridine with n-butyllithium. Trapping the lithiated species with various electrophiles afforded functionalized pyridines in good yields. A one-pot procedure also allowed the double functionalization at C4 and C2 in the case of 3-O-THP-pyridine. The ortho-metallating ability of this group was examined in comparison with other well-known oxygen-based ortho-directing groups
Dans une première partie, la protection des phénols et des pyridinols a été étudiée. Une nouvelle mé...
The stabilisation of 3,4-pyridyne (1) by an alkoxy group adjacent to the ring nitrogen is reported. ...
In this contribution, the first direct and efficient functionalization of the preformed 2-phenyltetr...
International audienceHerein we report regioselective deprotonations of 3- and 4-(tetrahydropyran-2-...
We report that the tetrahydropyranylation of pyridinols and phenols, exhibiting especially very low ...
International audienceA series of methoxy- and fluoro-pyridines have been deprotometalated in tetrah...
Regioselectivity is an important aspect in the design of organic protocols involving Directed ortho-...
Directed lithiation of substituted pyridines containing a directing metalating group (DMG) with a li...
Generally considered kinetic intermediates in addition reactions of alkyllithiums to pyridine, 1-lit...
This chapter addresses the genesis, reactivity and applications of oxygen-bearing lithium compounds ...
Regioselectivity is an important aspect in the design of organic protocols involving Directed <i>ort...
Synthesis and Functionalization via Direct Lithiation of α-Aryl-substituted Tetrahydropyran
Transition-metal mediated C–H functionalization has emerged as a powerful method in the chemistry re...
Dans une première partie, la protection des phénols et des pyridinols a été étudiée. Une nouvelle mé...
The ortho lithiation-trapping sequence of phenylaziridines is described. This methodology, which cou...
Dans une première partie, la protection des phénols et des pyridinols a été étudiée. Une nouvelle mé...
The stabilisation of 3,4-pyridyne (1) by an alkoxy group adjacent to the ring nitrogen is reported. ...
In this contribution, the first direct and efficient functionalization of the preformed 2-phenyltetr...
International audienceHerein we report regioselective deprotonations of 3- and 4-(tetrahydropyran-2-...
We report that the tetrahydropyranylation of pyridinols and phenols, exhibiting especially very low ...
International audienceA series of methoxy- and fluoro-pyridines have been deprotometalated in tetrah...
Regioselectivity is an important aspect in the design of organic protocols involving Directed ortho-...
Directed lithiation of substituted pyridines containing a directing metalating group (DMG) with a li...
Generally considered kinetic intermediates in addition reactions of alkyllithiums to pyridine, 1-lit...
This chapter addresses the genesis, reactivity and applications of oxygen-bearing lithium compounds ...
Regioselectivity is an important aspect in the design of organic protocols involving Directed <i>ort...
Synthesis and Functionalization via Direct Lithiation of α-Aryl-substituted Tetrahydropyran
Transition-metal mediated C–H functionalization has emerged as a powerful method in the chemistry re...
Dans une première partie, la protection des phénols et des pyridinols a été étudiée. Une nouvelle mé...
The ortho lithiation-trapping sequence of phenylaziridines is described. This methodology, which cou...
Dans une première partie, la protection des phénols et des pyridinols a été étudiée. Une nouvelle mé...
The stabilisation of 3,4-pyridyne (1) by an alkoxy group adjacent to the ring nitrogen is reported. ...
In this contribution, the first direct and efficient functionalization of the preformed 2-phenyltetr...