Filling a gap in the literature, this clearly structured book presents the much. Direct stereospecific synthesis of unprotected nh and nme aziridines from olefins jawahar l. Collection of czechoslovak chemical communications 2002, 67 9, 5965. The reaction of ntosyl imines with in situ generated iodomethyllithium, with a simple and rapid experimental protocol, allows an efficient and general synthesis of aziridines. Furthermore, intramolecular reactions and addition reactions are subdivided with respect to the mechanism of these reactions. First example of coupling reactions of fluoral, an amine and a diazo compound.
Selected examples for the synthesis of aziridines from alkenes r2 r1 r2 n x r1 r2 r1 xn singlet nitrene triplet nitrene xn h r2 r1 h x n h r2 r1 h x n h r2 r1 h x n j. A 50 ml round bottom flask was loaded with 1r, 4scamphor nitrimine 991. Direct stereospecific synthesis of unprotected nh and n. Aziridines are an important type of versatile building blocks for synthesis of diverse nitrogencontaining heterocyclic compounds and natural products. Jessing 1 n r activated aziridines r co2r, so2r and cor nonactivated aziridines r h, alkyl and aryl ho nh2 o so nh 2 o o n h aziridines can be synthesized in numerous ways including sn2 displacement, 14 addition. Because of the potential for increased efficiency and selectivity, along with the advantages of environmentally benign synthetic procedures, multicomponent. The reaction of azlactones with imines yielded both the synand theanti. In this field, chiral aziridines form an attractive class of compounds, since they are available in enantiomerically pure or highly enriched form by a variety of procedures and can be used for asymmetric synthesis in a number of different ways.
Chiral aziridines are prevalently found in natural products and artificially made bioactive molecules, thus receiving significant attention in the past decades. This coupling allows access to propargyl amines with pendent aziridine functionality. The aziridine structural motif, predominantly nh and to. The simplest and oldest preparation of aziridines is the ring closure of a.
Synthesis of ferrocenyl substituted aziridines zeytinci, serhat m. Pdf aziridines are important precursors for the synthesis of various nitrogencontaining bioactive molecules, such as heterocycles, alkaloids. Small ring heterocycles, such as epoxides and aziridines, are present in several natural products and are also highly versatile building blocks, frequently involved in the synthesis of numerous bioactive products and pharmaceuticals. Aminoalcohols 1ab in the presence of chlorosulfonic acid form sulfonic esters under mild conditions in quantitative yields.
Falck1 despite the prevalence of the nh aziridine motif in bioactive natural products and the clear. Synthesis of aziridines from alkenes and aryl azides with a reusable macrocyclic tetracarbene iron catalyst. To our knowledge, this was the first reported direct synthesis of a vinyl aziridine bearing a phosphorus group on nitrogen. Synthesis of aziridines from alkenes and aryl azides with a reusable macrocyclic tetracarbene iron catalyst journal of the american chemical society. Pdf a novel approach to the synthesis of optically pure 12aminoalkyl aziridines via a nucleophilic ringopening reaction of aziridine is. Synthesis and evaluation of biological activities of. General procedures for the synthesis of ndiphenylphosphinyl vinyl aziridines. Synthesis and reactions of aziridines via batch and flow.
Studies have been made on the possible synthesis of 1 arylethynylaziridines by oxidative condensation of phenylacetylene with aziridine and by alkylation of aziridine with 1halo2arylacetylenes. Hereby, an efficient synthesis of a wide range of new chiral aziridines is presented which can be applied as starting products for the synthesis of new heterocyclic compounds. Organocatalysis in synthesis and reactions of epoxides and aziridines. Aziridines, the triangular, comparably highly strained nitrogen analogs of epoxides, are important synthetic intermediates i. Aziridines, arylalanines, asymmetric synthesis, cobalt catalyst aziridines are useful intermediates for the synthesis of the amino alcohols, amino acids, and nitrogencontaining heterocycles. A general strategy for the synthesis of enantiomerically. Synthesis of chiral organocatalysts derived from aziridines. A reaction of a chiral aldimine derived from phenylalaninal proceeded with high diastereoselectivity. A nitrogen nucleophilic cyclization on the adjacent position bearing a leaving group and. A straightforward synthesis of aziridines is reported from electronrich azides, electrondeficient olefins, and. Aziridines and epoxides are among the most widely used intermediates in organic synthesis, acting as precursors to complex molecules due to the strains incorporated in their skeletons. This thesis describes the synthesis and ring opening reactions of aziridines performed under batch as well as continuous flow conditions.
General characteristics epoxides can be converted into aziridines by nucleophilic attack of azide ion, the staudinger reaction, and aziridine ring formation with. Pdf aziridines are important precursors for the synthesis of various nitrogen containing bioactive molecules, such as heterocycles, alkaloids. Pdf synthesis of chiral 12aminoalkylaziridines via a self. Carbonylation of aziridines as a powerful tool for the. These reactions proceed through a 1,3dipolar cycloaddition of dipolarophiles azlactones with dienophiles imines mediated by tmscl. Catalytic asymmetric synthesis of trisubstituted aziridines. Among the synthetic routes available to access this interesting scaffold, the carbonylation of aziridines, in which carbon monoxide is inserted into one of the ring carbonnitrogen bonds, is praised for its efficiency and remarkable regio. Pdf synthesis of oxazolinyl aziridines vito capriati. Synthesis and reactivity of 2 carboxymethylaziridine. Several drugs feature aziridine rings, including mitomycin c, porfiromycin, and azinomycin b carzinophilin. Encouraged by this promising result, we next examined the scope of the reaction by using the same anion and ndpp imines derived from 4bromo and 4fluorobenzaldehyde, furfural and 2,2dimethylpropionaldehyde.
Wenker synthesis is a typical method for synthesis of aziridines in which 2amino alcohols from natural or synthetic amino acids are cyclized by base. Chapter 1 gives a brief introduction to the synthesis and ring opening reactions of aziridines. A mechanism to explain this novel reaction is proposed. Paudyal, hongyin gao, qinglong xu,1 muhammed yousufuddin,2 deepa devarajan,3 daniel h. The synthesis of ntosylaziridines 7 was accomplished by basemediated cyclization of bistosylates 6 of 2amino alcohols 5 in water and dichloromethane in equal amounts scheme 1. In the areas of medicinal chemistry and chemical biology, aziridines are of current interest as starting materials for the preparation of peptides 23 and the synthesis of peptide. Besides their importance as reactive intermediates, many biologically active compounds also contain these threemembered rings. Facile synthesis of aziridines from imines and diazoesters or aldehydes, amines, and diazoesters using a catalytic amount of lanthanide triflate. Asymmetric synthesis of terminal ntertbutylsulfinyl. Ethyleneimine, stabilized appears as a clear colorless liquid with an ammonia like odor. Abstract synthesis of imidazolines from aziridines by michael robert kuszpit the majority of the work in this thesis presents a new method to syntheisize imidazolines. First method is the classical gabrielcromwell reaction and the. The parent compound is aziridine or ethylene imine, with molecular formula c 2 h 4 nh. In continuation of the studies on the synthesis and application of chiral aziridines 1,8,10,29,33, we used chiral aminoalcohols 1 to convert them into nh aziridines 2 via a modi.
Aziridines are valuable strained small heterocycles of interest in preparative organic synthesis. A onepot method for the synthesis of indolinefused pyrrolidines 325 scheme 107 by a domino ringopening cyclization of activated aziridines 324 with indoles 323 having substituents at c3. Aziridines ethylene imines are important building blocks in organic synthesis, because they allow for convenient access to amines, amino alcohols, diamines, and other useful nitrogencontaining molecules. General approaches to the asymmetric synthesis of aziridines through cyclization methods can be divided into two main categories.
Wulffs group has developed a robust catalytic asymmetric aziridination reaction providing. Chapter 2 gives a brief introduction to flow chemistry, and describes the synthesis of aziridines from 1,2amino alcohols, as well as their subsequent ring. Catalytic asymmetric synthesis of alkynyl aziridines. Asymmetric synthesis of trifluoromethylated aziridines. Aziridine is an organic compound consisting of the threemembered heterocycle ch 2 2 nh. Disappointingly, the yields of aziridines 25 obtained from. Aziridines are organic compounds containing the aziridine functional group, a threemembered heterocycle with one amine nr and two methylene bridges cr 2. Stereoselective multicomponent reactions in the synthesis. With the development of the catalytic asymmetric synthesis of trisubstituted aziridines presented here, it will be of interest to investigate the mechanistic di. The synthesis and applications of nalkenyl aziridines nicholas a. Aziridines can be synthesized in numerous ways including sn2 displacement, 14 addition, addition of carbenes, electrophiles, nitrenes and reduction h. Aziridine is a saturated organic heteromonocyclic parent, a member of aziridines and an azacycloalkane. Pdf a novel approach to the synthesis of optically pure 12aminoalkylaziridines via a nucleophilic ringopening reaction of aziridine is.
Asymmetric synthesis of cf2functionalized aziridines by. Imidazolines have been previously synthesized in the tepe group by the reaction of azlactones with imines. Alkaloids synthesis from aziridines as key advanced synthetic in termediates. The journal of organic chemistry 2008, 73 23, 94119416. The observed excellent yields, regioselectivities and enantioselectivities find no rivals in other organocatalytic aziridine synthesis. In addition, we have expanded this concept to the synthesis of enantiomerically pure, terminal alkyl aziridines. Synthesis of aziridine 2phosphonates and their biological activities babiz, hakan m. The synthesis of n tosylaziridines 7 was accomplished by basemediated cyclization of bistosylates 6 of 2amino alcohols 5 in water and dichloromethane in equal amounts scheme 1. Bicyclic aziridines, derivatives of 2,2,6,6tetramethyl4piperidone triacetoneamine, are synthesized, which by acids treatment undergo the nc1 or nc2 bonds cleavage to form the corresponding pyrrolines, pyrrolidines, and piperidines. Aziridine moieties occur in many natural products and are also encountered in unnatural biologically active compounds including drugs in clinical use, especially in the field of cancer treatment. Aziridines and epoxides in organic synthesis wiley.
The synthesis and applications of nalkenyl aziridines tspace. Though a variety of methods have been developed for the synthesis of aziridines, the simplest one is. Aziridines, the nitrogenous analogues of epoxides, have until recently excited far less interest amongst synthetic organic chemists than their oxygenated counterparts, with some justification. Most contemporary methods of chiral aziridine preparation have relied on the chiral pool. Asymmetric synthesis of aziridines and arylalanine derivatives. Butler september 16, 2004 introduction aziridines 1 have been synthetic targets as well as useful building blocks in synthesis since gabriels 1888 discovery of the smallest nitrogen containing heterocycle. Synthesis of trifluoromethyl aziridines in 1,1,1,3,3,3hexafluoropropan2ol. The intramolecular nucleophilic substitution reactions methods ia and ii involve attack of a nucleophilic amino. Aziridines are important precursors for the synthesis of various nitrogencontaining bioactive molecules, such as heterocycles, alkaloids and amino acids. Both enantiomers of cis aziridines from one enantiomer of the catalyst. Aziridines, besides the synthesis of pyrroles, have been employed in the synthesis of imidazolines, thiazolines, oxazolines, and 2,3dihydrobenzofurans. Rethinking their application and manipulation in synthesis christopher r.
Remarkably, both electronrich and electronpoor olefins are converted to aziridines with high efficiency. Lewis acidcatalyzed synthesis of aziridines the journal. Among them, the introduction of fluorine or fluoroalkyl groups into threemembered nheterocycles has emerged as an attractive direction due to the unique fluorine effect in pharmaceuticals and biology. Synthesis of aziridines from alkenes and aryl azides with. Synthesis of 2 carboxymethyl aziridines is effectuated via functional group transformations of compounds derived from the chiral pool or starting from 2formylaziridines.