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Toward the enantioselective total synthesis of lyngbyatoxin A: on the stereocontrolled introduction of the quaternary stereogenic centre

✍ Scribed by Janne E Tønder; David Tanner


Book ID
104205473
Publisher
Elsevier Science
Year
2003
Tongue
French
Weight
352 KB
Volume
59
Category
Article
ISSN
0040-4020

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✦ Synopsis


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 carrying a 7-substituted indole moiety.


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