A Palladium-Catalyzed Oxa-(4+4)-Cycloaddition Strategy Towards Oxazocine Scaffolds

Anaïs Scuiller; Xueyang Liu; Marie Cordier; Julian Garrec; Alexis Archambeau

doi:10.1055/s-0040-1706038

Synlett, Inhaltsverzeichnis

Synlett 2021; 32(10): 981-986
DOI: 10.1055/s-0040-1706038

letter

A Palladium-Catalyzed Oxa-(4+4)-Cycloaddition Strategy Towards Oxazocine Scaffolds

Authors

Anaïs Scuiller

^aLaboratoire de Synthèse Organique, UMR 7652, Ecole Polytechnique, ENSTA Paris, CNRS, IP Paris, 91128 Palaiseau, France
Xueyang Liu

^aLaboratoire de Synthèse Organique, UMR 7652, Ecole Polytechnique, ENSTA Paris, CNRS, IP Paris, 91128 Palaiseau, France
Marie Cordier

^bLaboratoire de Chimie Moléculaire, UMR 9168, Ecole Polytechnique, CNRS, IP Paris, 91128 Palaiseau, France
Julian Garrec∗

^cUnité Chimie et Procédés, ENSTA Paris, IP Paris, 91120 Palaiseau, France
Alexis Archambeau ∗

^aLaboratoire de Synthèse Organique, UMR 7652, Ecole Polytechnique, ENSTA Paris, CNRS, IP Paris, 91128 Palaiseau, France

Abstract

Alle Artikel dieser Rubrik

Abstract

A Pd-catalyzed oxa-(4+4)-cycloaddition between 1-azadienes and (2-hydroxymethyl)allyl carbonates is described. Aurone-derived azadienes furnished polycyclic 1,5-oxazocines in good yields. Interestingly, linear azadienes have also been involved and yielded monocyclic heterocycles with complete regioselectivity. DFT calculations were carried out to gain insight on this observation.

Key words

cycloaddition - catalysis - heterocycles - medium-sized rings - oxazocines - azadienes

Volltext

Referenzen

References and Notes
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21 CCDC 2040269 contains the supplementary crystallographic data for this paper. The data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/structures
22 CCDC 2040268 contains the supplementary crystallographic data for this paper. The data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/structures
23 See the Supporting Information.
24 Typical Procedure for the Pd-Catalyzed (4+4) Cycloadditions of 2a with 1a (Benzene, rt) In a screw-cap SVL tube filled with argon, Pd₂(dba)₃ (13.7 mg, 0.015 mmol, 0.05 equiv) and dppe (12.0 mg, 0.03 mmol, 0.1 equiv) were added in benzene (3 mL, 0.1 M) and stirred for 15 min at rt. Carbonate 2a (84.7 mg, 0.45 mmol, 1.5 equiv) and azadiene 1a (113 mg, 0.30 mmol) were then added, the reaction mixture was stirred at rt for 16 h, filtered over silica, and concentrated under reduced pressure to afford the crude product. The residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc = 85:15) to afford 3a (109 mg, 81%) as a yellow solid; mp 46 °C. IR (neat): 2922, 1597, 1494, 1452, 1384, 1346, 1180, 1157, 1095, 1069, 747 cm^–1. ¹H NMR (400 MHz, CDCl₃, –20 °C): δ = 7.86 (d, J = 8.2 Hz, 2 H), 7.61–7.58 (m, 1 H), 7.41–7.12 (m, 10 H), 5.45 (s, 1 H), 5.24 (s, 1 H), 5.02 (s, 1 H), 4.91 (d, J = 13.5 Hz, 1 H), 4.58 (d, J = 12.6 Hz, 1 H), 4.24 (d, J = 12.6 Hz, 1 H), 4.10 (d, J = 13.5 Hz, 1 H), 2.44 (s, 3 H). ¹³C NMR (101 MHz, CDCl₃, –20 °C): δ = 154.4, 153.0, 143.5, 139.3, 138.1, 136.4, 129.3 (2 C), 128.5, 128.4 (2 C), 127.8 (2 C), 127.6 (2 C), 126.6, 124.6, 123.1, 122.7, 120.0, 116.0, 111.3, 79.0, 75.9, 54.7, 21.6. HRMS (ESI⁺): m/z [M + H]⁺ calcd for C₂₆H₂₄NO₄S⁺: 446.1421; found: 446.1410.

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