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Methodologies in Amine Synthesis. Группа авторовЧитать онлайн книгу.

Methodologies in Amine Synthesis - Группа авторов


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involves radical ring opening of small cyclic systems, while the latter enables the effective functionalization of N‐containing alkyl chains.

Chemical reaction depicts the radical transposition processes using nitrogen-radicals.

      Mechanistically, 1,5‐HAT reactions of nitrogen radicals are strongly polarity‐ and enthalpy‐driven processes with stringent geometrical constraints. This means that three main factors need to be considered when approaching the design of these transformations.

       Geometrical factors. The 1,5‐HAT process goes through a six‐membered ring transition state, which, depending on the 3D structure of the nitrogen radical, might favor or thwart reactivity [8]. This is seen in a classical example of HLF reactivity for the assembly of a complex‐bridged azabicyclic system (Scheme 2.3a) [9]. Although the intermediate N‐chloroamine 6 contains four different sites with 1,5‐relationship to the aminium radical 7, only the geometrically proximal methyl group is functionalized (8).Scheme 2.2 1,5‐HAT process in HLF reaction.Scheme 2.3 Geometrical factors, polar and enthalpic effects in 1,5‐HAT process.Source: (a) Katohgi et al. [9] and (c) Luo [10].

       Polar effects. Nitrogen radicals are reactive intermediates with distinct and different philicities based on their substitution patterns. There are four general classes: (i) iminyl, (ii) amidyl (including carbamoyls, sulfamidyls, and phosphoramidyls), (iii) aminyl, and (iv) aminium radicals (Scheme 2.3b). The philicity and the hybridization of these species change significantly: iminyl radicals [11] are σ‐radicals with ambiphilic character, while all the others are π‐radicals with the amidyls [12] and the aminiums [13] being electrophilic and the aminyls [14] slightly nucleophilic.

       Although the 1,5‐HAT process goes via a sterically favorable six‐membered ring transition state, polar effects have a strong interplay in its stabilization [15]. This means that when the innate polarity of the H‐atom matches the one of the nitrogen radical, then a charge transfer stabilization takes place, leading to a more facile 1,5‐HAT process. As an example, the general amidyl radical 9 would undergo selective abstraction from the α‐O‐methylene group rather than the α‐ester one, as transition state 10 enables a better stabilization of polar effects than transition state 11.

       Enthalpic effects. The exothermicity, hence the feasibility, of 1,5‐HAT reactions is dictated by the relative energy difference between the sp3 C—H bond broken and the N—H bond formed [16]. In general, N—H bonds have higher bond‐dissociation energy (BDEs) than sp3 C—H bonds, which facilitate 1,5‐HAT reactivities (Scheme 2.3c) [10]. This is particularly evident for the reaction of amidyl and aminium radicals, which lead to the formation of very strong N—H bonds. Iminyl radicals have witnessed a more limited application in radical relay strategies owing to the weaker nature of their corresponding N—H bonds, which makes 1,5‐HAT possible mostly from activated or tertiary sp3 centers. Aminyl radicals are the only class of nitrogen radicals that are not used in these processes owing to their weaker N—H bonds and also to negative polar effects.

      2.3.1 Reductive Strategies

      2.3.1.1 1,5‐HAT via Iminyl Radicals

      Iminyl radicals have been identified as powerful reactive intermediates for a number of reactions such as intramolecular cyclization but also radical ring opening and 1,5‐HAT. In this case, the pioneering work of Forrester [17–20] has clearly demonstrated their ability to partake into radical transposition, but the harsh chemical methods for their generation limited applications in mainstream organic synthesis.

      The Leonori group recently reported that iminyl (and amidyl radicals) can be generated upon visible light irradiation from easy‐to‐make O‐aryl oximes [21] via oxidative quenching photoredox cycles and also via the formation of electron donor–acceptor (EDA) complex with tertiary amines [22–24]. These strategies have been adopted by others in the subsequent development of interrupted HLF‐type reactions.


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