Improved Synthesis of the Biologically Active Methionine Analog, L-2-Amino-4-methoxy-cis-but-3-enoic Acid (L-cis-amb) Using an Electrophilic Glycinate Synthon

Vitauts Alks Grace Cancer Drug Center

Janice R. Sufrin Grace Cancer Drug Center; Department of Surgical Oncology, Roswell Park Memorial Institute Buffalo, New York, 14263, USA

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Patrick Meffre & Philippe Durand. (2002) NEW ROUTES TO α-AMINO ACID β,γ-THIOENOL ETHER DERIVATIVES. Synthetic Communications 32:2, pages 287-296.
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M. Daumas, L. Vo-quang & F. Le Goffic. (1990) An Improved Synthesis of Methyl 2-N-formylamino-2-(dimethoxyphosphinyl)-acetate. Synthetic Communications 20:22, pages 3395-3401.
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. 1995. Comprehensive Organic Functional Group Transformations. Comprehensive Organic Functional Group Transformations 1085 1229 .

Alex C. Campbell & David R. Jaap. 1995. Comprehensive Organic Functional Group Transformations. Comprehensive Organic Functional Group Transformations 95 157 .

M. Daumas, L. Vo-Quang & F. Le Goffic. (1992) New non-proteogenic aminoacids bearing an enol aryl-ether moiety.. Tetrahedron 48:12, pages 2373-2384.
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V. ALKS & J. R. SUFRIN. (1990) ChemInform Abstract: Improved Synthesis of the Biologically Active Methionine Analog, L-2-Amino-4-methoxy-cis-but-3-enoic Acid (L-cis-amb) Using an Electrophilic Glycinate Synthon.. ChemInform 21:10.
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Vitauts Alks & Janice R. Sufrin. (1990) Improved synthetic access to the β,γ-enol ether amino acids, L-2-amino-4-methoxy-trans-but-3-enoic acid and l-2-amino-4-methoxy--but-3-enoic acid. Tetrahedron Letters 31:37, pages 5257-5260.
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Improved Synthesis of the Biologically Active Methionine Analog, L-2-Amino-4-methoxy-cis-but-3-enoic Acid (L-cis-amb) Using an Electrophilic Glycinate Synthon

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Improved Synthesis of the Biologically Active Methionine Analog, L-2-Amino-4-methoxy-cis-but-3-enoic Acid (L-cis-amb) Using an Electrophilic Glycinate Synthon

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