Transition-metal-catalyzed domino reactions of strained bicyclic alkenes

• Austin Pounder,
• Eric Neufeld,
• Peter Myler and
• William Tam

Beilstein J. Org. Chem. 2023, 19, 487–540, doi:10.3762/bjoc.19.38

• –Cu species 60 which after electrophilic amination with the O-benzoylhydroxylamine 54 liberates the final aminoborylated product 55 and a benzoyl–Cu complex 61. To close the catalytic cycle a transmetalation of 61 with LiOt-Bu regenerates the active catalyst. In 2017, Xiao and Fu studied the Cu

Diastereo- and enantioselective preparation of cyclopropanol derivatives

• Marwan Simaan and
• Ilan Marek

Beilstein J. Org. Chem. 2019, 15, 752–760, doi:10.3762/bjoc.15.71

• enantiomeric ratios (er up to 99:1, Scheme 7). Following the same concept of copper-catalyzed diastereo- and enantioselective carbomagnesiation reaction of cyclopropenes 6 followed now by a selective electrophilic amination reaction, a powerful entry to cyclopropylamines as single diastereoisomer and in

Asymmetric α-amination of 3-substituted oxindoles using chiral bifunctional phosphine catalysts

• Qiao-Wen Jin,
• Zhuo Chai,
• You-Ming Huang,
• Gang Zou and
• Gang Zhao

Beilstein J. Org. Chem. 2016, 12, 725–731, doi:10.3762/bjoc.12.72

• tetrasubstituted carbon center have been recognized as core building blocks for the preparation of many biologically active and therapeutic compounds [2][3][4][5][6][7]. As a type of commercially available electrophilic amination reagents, azodicarboxylates have been extensively used in both asymmetric

Copper-catalyzed intermolecular oxyamination of olefins using carboxylic acids and O-benzoylhydroxylamines

• Brett N. Hemric and
• Qiu Wang

Beilstein J. Org. Chem. 2016, 12, 22–28, doi:10.3762/bjoc.12.4

• . Keywords: copper; electrophilic amination; olefin oxyamination; Introduction The 1,2-oxyamino motif is highly valuable and found in a vast range of biologically active natural products, pharmaceuticals, and agrochemicals (Figure 1) [1][2]. Representative examples include salmeterol (Advair®), a β2

• transformation, integrating an electrophilic amination with a nucleophilic oxygenation, builds upon our recent development in copper-catalyzed olefin difunctionalization, such as copper-catalyzed diamination [40] and amino lactonization [34]. This strategy overcomes common issues of chemo- and regioselectivity

Continuous formation of N-chloro-N,N-dialkylamine solutions in well-mixed meso-scale flow reactors

• A. John Blacker and
• Katherine E. Jolley

Beilstein J. Org. Chem. 2015, 11, 2408–2417, doi:10.3762/bjoc.11.262

• -Chloramines provide a versatile and reactive class of reagents for use in electrophilic amination and other reactions. N-Chloro-N,N-dialkylamines have been shown to offer a broad range of products from reactions with i) unsaturated C–C bonds to give amines [1][2][3] and heterocycles [1][4]; ii) Grignard and

Multicomponent versus domino reactions: One-pot free-radical synthesis of β-amino-ethers and β-amino-alcohols

• Bianca Rossi,
• Nadia Pastori,
• Simona Prosperini and
• Carlo Punta

Beilstein J. Org. Chem. 2015, 11, 66–73, doi:10.3762/bjoc.11.10

• a) [29]. Surprisingly, the same reaction was even more efficient when performed in the presence of the Ti(IV)/Zn/t-BuOOH system (Scheme 2, entry b). Under the latter conditions, the domino approach was also successfully extended to cyclic ethers, promoting the consecutive electrophilic amination to

Synthesis of oleophilic electron-rich phenylhydrazines

• Aleksandra Jankowiak and
• Piotr Kaszyński

Beilstein J. Org. Chem. 2012, 8, 275–282, doi:10.3762/bjoc.8.29

• arylboronic acid V to AD [18][19][20]. The latter method is especially suited for arylhydrazides substituted with sensitive functional groups. Protected electron-rich arylhydrazines, hydrazides II, containing the 2,2,2-trichloroethyl group (R = CH2CCl3) are conveniently prepared by direct electrophilic

• amination of arenes VI with bis(2,2,2-trichloroethyl) azodicarboxylate (BTCEAD) under Lewis [21][22] or Brønsted [23] acid conditions. By judicious choice of the substituent R, the removal of the protecting group in II and formation of arylhydrazines I can be accomplished under acidic (R = t-Bu) [16