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title:(Stereocontrolled AND Introduction AND of AND the AND Quaternary AND Stereogenic AND Centre AND in AND Lyngbyatoxin AND A)

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1 Conference paper

Stereocontrolled Introduction of the Quaternary Stereogenic Centre in Lyngbyatoxin A

In our study of the enantioselective total synthesis of Lyngbyatoxin A, we have focused first on the stereocontrolled introduction of the quaternary stereogenic centre. The key step in the synthesis involves an enantiospecific Lewis-acid mediated rearrangement of chiral vinyl epoxides

Year: 2003

Language: English

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2 Journal article

Toward the Enantioselective Total Synthesis of Lyngbyatoxin A: On the Stereocontrolled Introduction of the Quaternary Stereogenic Centre

This paper deals with an approach to the enantioselective total synthesis of Lyngbyatoxin A, with focus on the stereocontrolled introduction of the quaternary stereogenic centre. The key step in the synthesis involves an enantiospecific Lewis-acid mediated rearrangement of chiral vinyl epoxides

Year: 2003

Language: English

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