POSITION AND DIENOPHILE DEPENDENT DIELS-ALDER REACTION OF VINYLCYCLOHEPTATRIENES

DOI: 10.1016/S0040-4039(00)85292-2

Source and publish data:

Tetrahedron Letters p. 5653 - 5656 (1986)

Update date:2022-08-03

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Authors:

Aga, Michihiro

Okada, Keiji

Oda, Masaji

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Article abstract of DOI:10.1016/S0040-4039(00)85292-2

While 1-vinyl- and 2-vinylcycloheptatrienes undergo Diels-Alder reactions excusively from cycloheptatriene forms at the diene part including the vinyl group, 3-vinylcycloheptatriene reacts site-selectively from either cycloheptatriene or norcaradiene form

Full text of DOI:10.1016/S0040-4039(00)85292-2

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Article Doi

POSITION AND DIENOPHILE DEPENDENT DIELS-ALDER REACTION OF VINYLCYCLOHEPTATRIENES

DOI: 10.1016/S0040-4039(00)85292-2

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)85292-2

Full text of DOI:10.1016/S0040-4039(00)85292-2

Products guided by the article

R&D Labs maybe for 108404-56-4

Relevant to this article

Heteroarotinoids. Synthesis, Characterization, and Biological Activity in Terms of an Assessment of These Systems To Inhibit the Induction of Ornithine Decarboxylase Activity and To Induce Terminal Differentiation of HL-60 Cells

Structure-Activity Studies on the C-Terminal Hexapeptide of Substance P with Modifications at the Glutaminyl and Methioninyl Residues

One-pot synthesis of diarylamines from two aromatic amines via oxidative dearomatization-imino exchange-reductive aromatization