947590-32-1Relevant academic research and scientific papers
Iron-Catalyzed Radical Acyl-Azidation of Alkenes with Aldehydes: Synthesis of Unsymmetrical β-Azido Ketones
Ge, Liang,Li, Yajun,Bao, Hongli
supporting information, p. 256 - 260 (2019/01/10)
An iron-catalyzed acyl-azidation of alkenes under mild reaction conditions has been developed. Aromatic aldehydes or aliphatic aldehydes can be used as the acyl radical precursors; TMSN3 is used as the azido source; TBHP is the initiator. The s
(Salen)Mn(III)-catalyzed chemoselective acylazidation of olefins
Zhang, Liang,Liu, Shuya,Zhao, Zhiguo,Su, Hongmei,Hao, Jingcheng,Wang, Yao
, p. 6085 - 6090 (2018/08/01)
We describe a (salen)Mn(iii)-catalyzed three-component reaction of aldehydes, olefins, and sodium azide for the installation of two useful groups (C═O and N3) into the double bond. Traditionally, (salen)Mn(iii) in conjunction with iodosobenzene is a classical catalysis system for epoxidation of olefins. Owing to the highly competitive oxygenation approaches, it is a true challenge to establish a distinct strategy for the exploration of new olefin transformations based on this (salen)Mn(iii) catalysis system. Herein, the key to this (salen)Mn(iii)-catalyzed acylazidation of olefins was the rational application of the distinct reactivity of oxomanganese(v) species which is capable of abstracting a hydrogen atom from a substrate C-H bond. This chemoselective reaction occurred in a precisely designed reaction sequence and tolerates complex molecular structures.
Photoinduced C-N bond cleavage in 2-azido-1,3-diphenyl-propan-1-one derivatives: Photorelease of hydrazoic acid
Klima, Rodney F.,Jadhav, Abhijit V.,Singh, Pradeep N. D.,Chang, Mingxin,Vanos, Christine,Sankaranarayanan, Jagadis,Vu, Mai,Ibrahim, Nazarin,Ross, Elaine,McCloskey, Shaun,Murthy, Rajesh S.,Krause, Jeanette A.,Ault, Bruce S.,Gudmundsdottir, Anna D.
, p. 6372 - 6381 (2008/02/11)
(Chemical Equation Presented) Photolysis of 3-azido-1,3-diphenyl-propan-1- one (1a) in toluene yields 1,3-diphenyl-propen-1-one (2), whereas irradiation of 3-azido-2,2-dimethyl-1,3-diphenyl-propan-1-one (1b) results in the formation of mainly 2,2-dimethyl-1,3-diphenyl-propan-1-one. Laser flash photolysis (308 nm) of 1a,b in acetonitrile reveals a transient absorption (λmax = ～310 nm) due to the formation of radicals 4a and 4b, respectively, which have lifetimes of ～14 μs at ambient temperature. TD-DFT calculations (B3LYP/6-31+G(d)) reveal that the first and second excited states of the triplet ketone (T1K (n,π*) and T2K (π,π*)) in azide 1a are almost degenerate, at ～74 and 76 kcal/mol above the ground state (S0), respectively. Similarly, azide 1b has T1K and T2K 75 and 82 kcal/mol above S0, respectively. The calculated transition state for cleaving the C-N bond is located 71 and 74 kcal/mol above S0 in azides 1a and 1b, respectively. The calculated bond dissociation energies for breaking the C-N bond are 55 and 58 kcal/mol for azides 1a and 1b, respectively, making C-N bond breakage accessible from T 1K in azides 1 at ambient temperature. In comparison, the irradiation of azides 1 in argon matrices at 14 K lead to the formation of the corresponding triplet alkyl nitrenes (1-n), via intramolecular energy transfer from T2K- The characterization of 1-n was supported by isotope labeling, IR spectroscopy, and molecular modeling.
