INTRAMOLECULAR HETERO-DIELS-ALDER REACTION OF PROLINAL-DERIVED N-ARYLIMINES LEWIS ACID-DEPENDENT REVERSAL OF THE DIASTEREOSELECTIVITY | Health & Environmental Research Online (HERO)

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Citation
Tags

HERO ID

7648964

Reference Type

Journal Article

Title

INTRAMOLECULAR HETERO-DIELS-ALDER REACTION OF PROLINAL-DERIVED N-ARYLIMINES LEWIS ACID-DEPENDENT REVERSAL OF THE DIASTEREOSELECTIVITY

Author(s)

Linkert, F; Laschat, S; ,

Year

1994

Is Peer Reviewed?

Journal

Synlett
ISSN: 0936-5214
EISSN: 1437-2096

Publisher

GEORG THIEME VERLAG

Location

STUTTGART

Volume

1994

Issue

Page Numbers

125-126

Language

English

DOI

10.1055/s-1994-22764

Web of Science Id

WOS:A1994MW19600012

Abstract

Intramolecular Lewis acid-catalyzed hetero-Diels-Alder reaction of L-prolinal-derived N-arylimine 1 yielded diastereoselectively either the cis,cis-diazacyclopenta[a]anthracene derivative 2a or the trans,trans-isomer 2b, depending on the Lewis acid.