Volume 27, Issue 18
Natural Products
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ChemInform Abstract: Photocyclization of Enaminoesters: Access to 2,3-Dihydroindoles Spiroimides.

M. IBRAHIM-OUALI

M. IBRAHIM-OUALI

Lab. Chim. Subst. Nat, CNRS, Univ. Blaise Pascal, F-63177 Aubiere, Fr.

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M.-E. SINIBALDI

M.-E. SINIBALDI

Lab. Chim. Subst. Nat, CNRS, Univ. Blaise Pascal, F-63177 Aubiere, Fr.

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Y. TROIN

Y. TROIN

Lab. Chim. Subst. Nat, CNRS, Univ. Blaise Pascal, F-63177 Aubiere, Fr.

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J.-C. GRAMAIN

J.-C. GRAMAIN

Lab. Chim. Subst. Nat, CNRS, Univ. Blaise Pascal, F-63177 Aubiere, Fr.

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First published: April 30, 1996

Abstract

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ChemInform Abstract

The key step in this approach to the interesting title imides, e.g. (X) , is the photochemical reaction of the intermediate (V). The transformation of these synthons to the known precursors of Aspidosperma alkaloids such as (IX) and (XII) is also performed.

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