(Q58443867)

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Allylboration-reactions, the key to a short synthesis of benzoyl-pedamide

article published in 1992

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Allylboration-reactions, the key to a short synthesis of benzoyl-pedamide (English)

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Reinhard W. Hoffmann

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1

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Achim Schlapbach

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2

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publication date

January 1992

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published in

Tetrahedron

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volume

48

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issue

11

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page(s)

1959-1968

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Total synthesis of (+)-pederin. 2. Stereocontrolled synthesis of (+)-benzoylselenopederic acid and total synthesis of (+)-pederin

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Stereoselective synthesis of alcohols, XLI. Chirality transfer to generate quaternary stereogenic centers by an allylboration reaction

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Structure of bryostatin. 4. An important antineoplastic constituent of geographically diverse Bugula neritina (Bryozoa)

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Bioactive marine metabolites. Part 16. Calyculin A. A novel antitumor metabolite from the marine sponge Discodermia calyx

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Isolation and structure elucidation of onnamide A, a new bioactive metabolite of a marine sponge, Theonella sp

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Mycalamide A, an antiviral compound from a New Zealand sponge of the genus Mycale

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10.1016/S0040-4020(01)88867-0

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(Q58443867)

Allylboration-reactions, the key to a short synthesis of benzoyl-pedamide

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