π Complexes with Annellated Cyclobutene Rings: Bicyclo[3.2.0]heptadienyl Anion and Benzocyclobutene as Ligands for Transition Metals

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OriginalspracheEnglisch
Seiten (von - bis)680-691
Seitenumfang12
FachzeitschriftSYNLETT
Ausgabenummer6
PublikationsstatusVeröffentlicht - 1999

Abstract

As was first found on the basis of DSC measurements, bicyclo[3.2.0]heptadienyl cobalt complex 17 undergoes a ring opening - cycloaddition sequence at high temperature with formation of ring expansion products. Benzocyclobutene complexes react in a similar way only in one case. However, deprotonation of benzocyclobutenol complex endo-31 results in a dramatic decrease of the ring opening temperature and allows corresponding [4+2] cycloaddition reactions at low temperature. Benzocyclobutenedione complex 74 shows interesting structural features, its fragmentation in the mass spectrometer leads to η6 coordinated benzyne chromium cation. Addition of vinylmetal reagents induces a dianionic oxy-Cope rearrangement at -78°C, the first case of such a reaction at such mild reaction conditions. Products are benzannellated cyclooctenediones and their intramolecular aldol adducts, which are obtained with very high diastereoselectivity.

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π Complexes with Annellated Cyclobutene Rings: Bicyclo[3.2.0]heptadienyl Anion and Benzocyclobutene as Ligands for Transition Metals. / Butenschön, Holger.
in: SYNLETT, Nr. 6, 1999, S. 680-691.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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title = "π Complexes with Annellated Cyclobutene Rings: Bicyclo[3.2.0]heptadienyl Anion and Benzocyclobutene as Ligands for Transition Metals",
abstract = "As was first found on the basis of DSC measurements, bicyclo[3.2.0]heptadienyl cobalt complex 17 undergoes a ring opening - cycloaddition sequence at high temperature with formation of ring expansion products. Benzocyclobutene complexes react in a similar way only in one case. However, deprotonation of benzocyclobutenol complex endo-31 results in a dramatic decrease of the ring opening temperature and allows corresponding [4+2] cycloaddition reactions at low temperature. Benzocyclobutenedione complex 74 shows interesting structural features, its fragmentation in the mass spectrometer leads to η6 coordinated benzyne chromium cation. Addition of vinylmetal reagents induces a dianionic oxy-Cope rearrangement at -78°C, the first case of such a reaction at such mild reaction conditions. Products are benzannellated cyclooctenediones and their intramolecular aldol adducts, which are obtained with very high diastereoselectivity.",
keywords = "Benzocyclobutene complexes, Bicyclo[3.2.0]heptadienyl complexes, Chromium, Cobalt, Dianionic oxy-Cope rearrangement",
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doi = "10.1055/s-1999-2700",
language = "English",
pages = "680--691",
journal = "SYNLETT",
issn = "0936-5214",
publisher = "Georg Thieme Verlag",
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TY - JOUR

T1 - π Complexes with Annellated Cyclobutene Rings

T2 - Bicyclo[3.2.0]heptadienyl Anion and Benzocyclobutene as Ligands for Transition Metals

AU - Butenschön, Holger

PY - 1999

Y1 - 1999

N2 - As was first found on the basis of DSC measurements, bicyclo[3.2.0]heptadienyl cobalt complex 17 undergoes a ring opening - cycloaddition sequence at high temperature with formation of ring expansion products. Benzocyclobutene complexes react in a similar way only in one case. However, deprotonation of benzocyclobutenol complex endo-31 results in a dramatic decrease of the ring opening temperature and allows corresponding [4+2] cycloaddition reactions at low temperature. Benzocyclobutenedione complex 74 shows interesting structural features, its fragmentation in the mass spectrometer leads to η6 coordinated benzyne chromium cation. Addition of vinylmetal reagents induces a dianionic oxy-Cope rearrangement at -78°C, the first case of such a reaction at such mild reaction conditions. Products are benzannellated cyclooctenediones and their intramolecular aldol adducts, which are obtained with very high diastereoselectivity.

AB - As was first found on the basis of DSC measurements, bicyclo[3.2.0]heptadienyl cobalt complex 17 undergoes a ring opening - cycloaddition sequence at high temperature with formation of ring expansion products. Benzocyclobutene complexes react in a similar way only in one case. However, deprotonation of benzocyclobutenol complex endo-31 results in a dramatic decrease of the ring opening temperature and allows corresponding [4+2] cycloaddition reactions at low temperature. Benzocyclobutenedione complex 74 shows interesting structural features, its fragmentation in the mass spectrometer leads to η6 coordinated benzyne chromium cation. Addition of vinylmetal reagents induces a dianionic oxy-Cope rearrangement at -78°C, the first case of such a reaction at such mild reaction conditions. Products are benzannellated cyclooctenediones and their intramolecular aldol adducts, which are obtained with very high diastereoselectivity.

KW - Benzocyclobutene complexes

KW - Bicyclo[3.2.0]heptadienyl complexes

KW - Chromium

KW - Cobalt

KW - Dianionic oxy-Cope rearrangement

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U2 - 10.1055/s-1999-2700

DO - 10.1055/s-1999-2700

M3 - Article

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SP - 680

EP - 691

JO - SYNLETT

JF - SYNLETT

SN - 0936-5214

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ER -

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