ChemInform Abstract: Synthesis of the ABH Rings of Ecteinascidin 597 Using a Connective Pummerer-Type Cyclization

ChemInform Abstract: Synthesis of the ABH Rings of Ecteinascidin 597 Using a Connective Pummerer-Type Cyclization

A connective Pummerer-type cyclization involving a N-protected glyoxamide (I) and a cysteine derivative (II) is applied to an asymmetric synthesis of the protected ABH rings of ecteinascidin 597. [PUBLICATION ABSTRACT]

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Veröffentlicht in:ChemInform 2012-02, Vol.43 (7), p.no-no
Hauptverfasser: Smith, Laura H. S., Nguyen, Trung Thanh, Sneddon, Helen F., Procter, David J.
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Sprache:eng
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alkaloids
ring closure reactions
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container_issue 7
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container_title ChemInform
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creator Smith, Laura H. S.
Nguyen, Trung Thanh
Sneddon, Helen F.
Procter, David J.
description A connective Pummerer-type cyclization involving a N-protected glyoxamide (I) and a cysteine derivative (II) is applied to an asymmetric synthesis of the protected ABH rings of ecteinascidin 597. [PUBLICATION ABSTRACT]
doi_str_mv 10.1002/chin.201207198
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source Wiley Online Library Journals Frontfile Complete
subjects alkaloids
ring closure reactions
title ChemInform Abstract: Synthesis of the ABH Rings of Ecteinascidin 597 Using a Connective Pummerer-Type Cyclization
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