Synthesis of photo- and ionochromic N-acylated 2-(aminomethylene)benzo[b]thiophene-3(2Н)-ones with a terminal phenanthroline group

• Vladimir P. Rybalkin,
• Sofiya Yu. Zmeeva,
• Lidiya L. Popova,
• Irina V. Dubonosova,
• Olga Yu. Karlutova,
• Oleg P. Demidov,
• Alexander D. Dubonosov and
• Vladimir A. Bren

Beilstein J. Org. Chem. 2024, 20, 552–560, doi:10.3762/bjoc.20.47

• “overall quantum yield” is used in Table 1 [29]. The formation of the short-lived E-isomer was earlier observed only in vitrified solvents at 77 K or under flash photolysis conditions [14]. As such, the parameters of the thermal acyl migration under steady-state irradiation conditions were not determined

Iridium-catalyzed hydroacylation reactions of C1-substituted oxabenzonorbornadienes with salicylaldehyde: an experimental and computational study

• Angel Ho,
• Austin Pounder,
• Krish Valluru,
• Leanne D. Chen and
• William Tam

Beilstein J. Org. Chem. 2022, 18, 251–261, doi:10.3762/bjoc.18.30

• experiment has been carried out under iridium catalysis. As such, we set out to explore the possibility acyl migration is favored over hydride migration in iridium-catalyzed hydroacylation reactions (Figure 2). Beginning with the two exo-η2-coordinated intermediates IN1a and IN1b, two possible transition

• states for the acyl migration, which exhibit a distorted Ir–C–C’–C’’ four-membered ring geometry, can be located. Directly comparing the hydrometalation process (Figure 1) to the carbometalation process, we see that acyl migration is unfavored, exhibiting activation energies of 19.2 (1bTS2d) to 20.7

• an activation energy of 4.8 to 5.6 kcal/mol, respectively, to produce the aforementioned thermodynamically stable Ir(I) alkoxide intermediates INa3 and INb3. Based on the extremely high energy barrier required for acyl migration over hydride migration, we hypothesize iridium-catalyzed hydroacylation

Progress and challenges in the synthesis of sequence controlled polysaccharides

• Giulio Fittolani,
• Theodore Tyrikos-Ergas,
• Denisa Vargová,
• Manishkumar A. Chaube and
• Martina Delbianco

Beilstein J. Org. Chem. 2021, 17, 1981–2025, doi:10.3762/bjoc.17.129

Synthesis of monophosphorylated lipid A precursors using 2-naphthylmethyl ether as a protecting group

• Jundi Xue,
• Ziyi Han,
• Gen Li,
• Khalisha A. Emmanuel,
• Cynthia L. McManus,
• Qiang Sui,
• Dongmian Ge,
• Qi Gao and
• Li Cai

Beilstein J. Org. Chem. 2020, 16, 1955–1962, doi:10.3762/bjoc.16.162

• helps avoiding the problematic acyl migration often observed with similar molecules [28]. In addition, the 4,6-O-naphthylidene acetal (e.g., in compounds 23 and 30) can be regioselectively opened at O6 or O4 under different conditions [19][29]. This could potentially allow the incorporation of other

Synthesis of acylglycerol derivatives by mechanochemistry

• Karen J. Ardila-Fierro,
• Andrij Pich,
• Marc Spehr,
• José G. Hernández and
• Carsten Bolm

Beilstein J. Org. Chem. 2019, 15, 811–817, doi:10.3762/bjoc.15.78

• ). However, purification of 4a by column chromatography on SiO2 favored acyl migration in 4a, thereby dropping the yield of 4a by increasing the amount of the isomeric sn-2,3-protected monoacylglycerol 4a’ (Figure 2) [42]. Typically, cobalt complex (S,S)-cat has been used for kinetic resolution of racemic

• by an aqueous work-up gave DAG 6a in only 31% yield, together with concomitant acyl migration of the corresponding sn-1,2-diacylglycerol 6a into sn-1,3-diacylglycerol 6a’. Therefore, the desilylation reaction was carried out by stirring 5a and BF3·CH3CN (Scheme 5a). Next, DAG 6a was reacted with 4

• through acyl migration of 6a under the basic milling conditions. Subsequently, the reaction mixture containing 8a and 8a’ was milled with 7-hydroxycoumarin (9) and triethylamine to achieve the conjugation of the DAGs 8 in 53% yield after two steps (Scheme 5c). A mixture of 10a and 10a’ (10a/10a’ 72:28

Rearrangements of organic peroxides and related processes

• Ivan A. Yaremenko,
• Vera A. Vil’,
• Dmitry V. Demchuk and
• Alexander O. Terent’ev

Beilstein J. Org. Chem. 2016, 12, 1647–1748, doi:10.3762/bjoc.12.162

Diastereoselective synthesis of new O-alkylated and C-branched inositols and their corresponding fluoro analogues

• Charlotte Collet,
• Françoise Chrétien,
• Yves Chapleur and
• Sandrine Lamandé-Langle

Beilstein J. Org. Chem. 2016, 12, 353–361, doi:10.3762/bjoc.12.39

• and scyllo-22 derivatives, which were not acetylated on the tertiary position; in order to avoid the acyl migration. The treatment of myo-22 with KF, 18-crown-6 in acetonitrile [53] at room temperature (optimal conditions) furnished the fluorinated compound myo-25 in 70% yield. The 19F NMR spectrum

DBU-promoted carboxylative cyclization of o-hydroxy- and o-acetamidoacetophenone

• Wen-Zhen Zhang,
• Si Liu and
• Xiao-Bing Lu

Beilstein J. Org. Chem. 2015, 11, 906–912, doi:10.3762/bjoc.11.102

• -diazabicycloundec-7-ene (DBU) is reported. This reaction provides convenient access to the biologically important compounds 4-hydroxy-2H-chromen-2-one and 4-hydroxy-2(1H)-quinolinone in moderate to good yields using carbon dioxide as the carboxylation reagent. An acyl migration from nitrogen to carbon is observed

• in the reaction of o-acetamidoacetophenone. Keywords: acyl migration; carbon dioxide; carboxylation; cyclization; condensation; Introduction 4-Hydroxy-2H-chromen-2-ones and 4-hydroxy-2(1H)-quinolinones are key structural subunits found in many natural products [1], commercial drugs [2][3] and

• cyclization of o-hydroxy- and o-acetamidoacetophenones with carbon dioxide to give 4-hydroxy-2H-chromen-2-ones and 4-hydroxy-2(1H)-quinolinones, respectively, in moderate to good yields under mild reaction conditions. An acyl migration from the nitrogen to carbon is observed in the reaction of o

Isocyanide-based multicomponent reactions towards cyclic constrained peptidomimetics

• Gijs Koopmanschap,
• Eelco Ruijter and
• Romano V.A. Orru

Beilstein J. Org. Chem. 2014, 10, 544–598, doi:10.3762/bjoc.10.50

• peptidomimetic design, the incorporation of N-protected aldehydes 4 (Scheme 2) is of great importance since deprotection of the α-adduct 5 allows acyl-migration and give access to α-hydroxy-β-amino amide derivatives 7 that possess important biological properties. This Passerini–amine deprotection–acyl migration

• , yielding pyrrazol-3-ones 107. The authors assumed that the cyclization proceeds via an N–C acyl migration of the trifluoroacetyl group, based on the labile character of the latter moiety (Scheme 33). In contrast, acid-promoted cyclization cleaved the trifluoroacetyl group and revealed the initially

An efficient method for the construction of polysubstituted 4-pyridones via self-condensation of β-keto amides mediated by P₂O₅ and catalyzed by zinc bromide

• Liquan Tan,
• Peng Zhou,
• Cui Chen and
• Weibing Liu

Beilstein J. Org. Chem. 2013, 9, 2681–2687, doi:10.3762/bjoc.9.304

• , when R is aryl, a 1,3-acyl migration occurred from N to C of intermediate 6 [35][36][37][38][39], and affords imine 7 and its equilibrium compound 8, the subsequent intramolecular nucleophilic cyclization of intermediate 8 provides the final product 4-pyridones [20][38]. Alternatively, when R is

• aliphatic, the 1,3-acyl migration is not observed – maybe the migration leads to an unstable imine intermediate. Therefore, under the acidic conditions, a cationic species 10 is generated from the intermediate 6 and the subsequent intramolecular dehydration process provides 2-pyridones 11 [19]. Conclusion

• In summary, we have established an improved efficient synthetic protocol for the synthesis of 4-pyridone derivatives by a sequence of intermolecular dehydration of β-keto amides in the presence of phosphorus pentoxide (P2O5), 1,3-acyl migration and intramolecular dehydration. Comparing to the similar

Asymmetric desymmetrization of meso-diols by C₂-symmetric chiral 4-pyrrolidinopyridines

• Hartmut Schedel,
• Keizo Kan,
• Yoshihiro Ueda,
• Kenji Mishiro,
• Keisuke Yoshida,
• Takumi Furuta and
• Takeo Kawabata

Beilstein J. Org. Chem. 2012, 8, 1778–1787, doi:10.3762/bjoc.8.203

• associated with the higher mono/diacylation ratio in the asymmetric acylation of 22a promoted by 14 (Table 6, entries 6–8). (Notice: Enantioenriched 23a gradually undergoes partial racemization when it is kept as a CHCl3 solution probably via intramolecular acyl migration: e.g., from 88% ee to 71% ee after

N-Heterocyclic carbene-catalyzed direct cross-aza-benzoin reaction: Efficient synthesis of α-amino-β-keto esters

• Takuya Uno,
• Yusuke Kobayashi and
• Yoshiji Takemoto

Beilstein J. Org. Chem. 2012, 8, 1499–1504, doi:10.3762/bjoc.8.169

• the privileged structure (Figure 1), and two main distinct approaches based on the bond-forming position have been developed. One approach utilizes Cα–Cβ bond formations, such as (a) acylation of Schiff bases or α-isocyano esters with acyl halides [4][15][16][17], and (b) intramolecular N–C acyl

• migration of the N-acyl glycine derivatives [18]. The other consists of C–N bond-forming reactions, such as (c) a rhodium-catalyzed N–H insertion reaction with α-diazo-β-keto esters [19][20][21], and (d) α-oxidation of β-keto esters to the corresponding oximes and the subsequent hydrogenation [22]. However

Alkoxide-induced ring opening of bicyclic 2-vinylcyclobutanones: A convenient synthesis of 2-vinyl-substituted 3-cycloalkene-1-carboxylic acid esters

• Xiufang Ji,
• Zhiming Li,
• Quanrui Wang and
• Andreas Goeke

Beilstein J. Org. Chem. 2012, 8, 650–657, doi:10.3762/bjoc.8.72

• [1,2]- and [1,3]-acyl migration of 2-vinylcyclobutanones, leading to cyclopentenones or cyclohexenones, respectively [15]. Danheiser and co-workers reported an oxyanion-accelerated [1,3]-rearrangement of in situ reduced 2-vinylcyclobutanones, by applying mixtures of LiBu3BH-MeLi and HMPT to give

Solvent- and ligand-induced switch of selectivity in gold(I)-catalyzed tandem reactions of 3-propargylindoles

• Estela Álvarez,
• Delia Miguel,
• Patricia García-García,
• Manuel A. Fernández-Rodríguez,
• Félix Rodríguez and
• Roberto Sanz

Beilstein J. Org. Chem. 2011, 7, 786–793, doi:10.3762/bjoc.7.89

• of 3-propargylindoles. Keywords: catalysis; gold; indoles; Nazarov cyclizations; selectivity; Introduction Catalysis with gold complexes as carbophilic π-acids has become a highly developed area in the last decade [1][2][3][4][5][6][7]. In particular, 1,2-acyl migration reactions of propargylic

Synthesis of 6-PEtN-α-D-GalpNAc-(1–>6)-β-D-Galp-(1–>4)-β-D-GlcpNAc-(1–>3)-β-D-Galp-(1–>4)-β-D-Glcp, a Haemophilus influenzae lipopolysacharide structure, and biotin and protein conjugates thereof

• Andreas Sundgren,
• Martina Lahmann and
• Stefan Oscarson

Beilstein J. Org. Chem. 2010, 6, 704–708, doi:10.3762/bjoc.6.80

• thioglycoside 4 [14] yielded the 6-O-silylated compound 5 (92%), benzylation of which gave donor 6 (85%). A benzyl group in the 4-position was preferred to an ester group to avoid the risk of acyl migration during subsequent reactions; desilylation, glycosidation and phosphorylation. 3II,4II-Diols of lactose

Investigation of acetyl migrations in furanosides

• O. P. Chevallier and
• M. E. Migaud

Beilstein J. Org. Chem. 2006, 2, No. 14, doi:10.1186/1860-5397-2-14

• , arabinoside and xyloside) derivatives facilitate acyl migration. Conditions which favour intramolecular and intermolecular mechanisms have been identified with intermolecular transesterifications taking place under mild basic conditions when intramolecular orthoester formations are disfavoured. In acetyl

• ribosides, acyl migration could be prevented when desilylation was catalysed by cerium ammonium nitrate. Introduction Over the years, a number of methods aimed at achieving chemoselective acylation of carbohydrates have been developed.[1][2][3] In addition to the challenges encountered in the selective

• characterisations have been limited.[9][10][11] Whilst attempting the synthesis of 1-O-acetyl, 2,3-isopropylidene riboside 1a from the 5-O-silylated precursor 1 (Scheme 1) using mild desilylating conditions, three compounds were isolated, evidently products of acyl migration processes. In order to synthesise