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ChemInform Abstract: Reversal of the Diastereoselectivity in a Sequence of Cycloaddition Reactions: (2 + 2 + 2), Ene Type, (4 + 2). A Totally Stereoselective Access to the Basic Skeleton of the Kaurane Family.

✍ Scribed by P. CRUCIANI; C. AUBERT; M. MALACRIA

Book ID: 112031597
Publisher: John Wiley and Sons
Year: 2010
Weight: 30 KB
Volume: 27
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199619224

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📜 SIMILAR VOLUMES

A stereoselective access to the basic sk

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A strategy based upon a "cascade" of three consecutive cycloaddition reactions [3+2], [2+2+2] and [4+2] allowed a stereoselective and straightforward access to the phyllocladane basic skeleton in eight high yield steps starting from 1,5-hexadiyne.

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ChemInform Abstract: A Mild Alternative

ChemInform Abstract: A Mild Alternative to the Use of Benzyne in (4 + 2) Cycloaddition Reactions.

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ChemInform Abstract: Cyano Diels—Alder a

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ChemInform Abstract: π-Facial Diastereos

ChemInform Abstract: π-Facial Diastereoselectivity in the (4 + 2) Cycloaddition of Singlet Oxygen as a Mechanistic Probe

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ChemInform Abstract: First Example of a Total Axial to Centered Chirality Transfer in the [2 + 2 + 2] Cycloadditions of Allenediynes.

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