ChemInform Abstract: BASE CATALYZED REARRANGEMENTS INVOLVING YLIDE INTERMEDIATES. PART 4. (1,3)SIGMATROPIC REARRANGEMENTS OF 4‐DIMETHYLAMINOBUTENES AND (3,3)SIGMATROPIC REARRANGEMENTS OF 3‐DIMETHYLAMINOHEXA‐1,5‐DIENES

Jemison, Robert W.; OLLIS, W. D.; Sutherland, I. O.; Tannock, J.

doi:10.1002/chin.198038125

Chemischer Informationsdienst

1980

DOI: 10.1002/chin.198038125

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ChemInform Abstract: BASE CATALYZED REARRANGEMENTS INVOLVING YLIDE INTERMEDIATES. PART 4. (1,3)SIGMATROPIC REARRANGEMENTS OF 4‐DIMETHYLAMINOBUTENES AND (3,3)SIGMATROPIC REARRANGEMENTS OF 3‐DIMETHYLAMINOHEXA‐1,5‐DIENES

Robert W. Jemison¹,

W. D. OLLIS²,

I. O. Sutherland³

et al.

Abstract: Die [lßl‐sigmatrope Umlagerung des Fluorenderivats (I) ist ein stereoselektiver Prozeß (eingehende Untersuchung): Es werden zwei racemische Diastereomere des Isomeren (II) im Verhältnis 16:3 gebildet.

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ChemInform Abstract: BASE CATALYZED REARRANGEMENTS INVOLVING YLIDE INTERMEDIATES. PART 4. (1,3)SIGMATROPIC REARRANGEMENTS OF 4‐DIMETHYLAMINOBUTENES AND (3,3)SIGMATROPIC REARRANGEMENTS OF 3‐DIMETHYLAMINOHEXA‐1,5‐DIENES

Abstract: Die [lßl‐sigmatrope Umlagerung des Fluorenderivats (I) ist ein stereoselektiver Prozeß (eingehende Untersuchung): Es werden zwei racemische Diastereomere des Isomeren (II) im Verhältnis 16:3 gebildet.

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References 1 publication

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