Synthesis of E and Z diastereoisomers of benzyl methyl-2-[3-(N-substituted)indolyl] cyclopropane-1,1-dicarboxylates and their stereoselective reductive cleavage

Article abstract of DOI:10.1080/00397919608003756

A synthesis and separation procedure is described for the E and Z diastereoisomers of indolyl-cyclopropane dicarboxylates, IV and V, potential intermediates in the synthesis of the corresponding E and Z cyclopropyl analogs of the amino acid tryptophan and

Full text of DOI:10.1080/00397919608003756

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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Synthesis of E and Z
Diastereoisomers of
Benzyl Methyl-2-[3-(N-
Substituted)indolyl]
Cyclopropane-1,1-
dicarboxylates and Their
Stereoselective Reductive
Cleavage
Tilak T. Raj a & Maurice R. Eftink a
a Department of Chemistry , University of
Mississippi, University , MS, 38677, USA
Published online: 21 Aug 2006.
To cite this article: Tilak T. Raj & Maurice R. Eftink (1996) Synthesis of E and Z
Diastereoisomers of Benzyl Methyl-2-[3-(N-Substituted)indolyl] Cyclopropane-1,1-
dicarboxylates and Their Stereoselective Reductive Cleavage, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 26:18, 3503-3509, DOI: 10.1080/00397919608003756
To link to this article: http://dx.doi.org/10.1080/00397919608003756
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