ChemInform Abstract: A Concise Synthesis of a Very Late Antigen‐4 Antagonist trans‐4‐[1‐[ [2,5‐Dichloro‐4‐(1‐methyl‐3‐indolylcarboxyamide)phenyl]acetyl] ‐(4S)‐methoxy‐(2S)‐pyrrolidinylmethoxy]cyclohexanecarboxylic Acid (V) via Reductive Etherification.

Chiba, Jun; Muro, Fumihito; Setoguchi, Masaki; Machinaga, Nobuo

doi:10.1002/chin.201249119

ChemInform

2012

DOI: 10.1002/chin.201249119

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ChemInform Abstract: A Concise Synthesis of a Very Late Antigen‐4 Antagonist trans‐4‐[1‐[ [2,5‐Dichloro‐4‐(1‐methyl‐3‐indolylcarboxyamide)phenyl]acetyl] ‐(4S)‐methoxy‐(2S)‐pyrrolidinylmethoxy]cyclohexanecarboxylic Acid (V) via Reductive Etherification.

Jun Chiba

Fumihito Muro

Masaki Setoguchi

et al.

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ChemInform Abstract: A Concise Synthesis of a Very Late Antigen‐4 Antagonist trans‐4‐[1‐[ [2,5‐Dichloro‐4‐(1‐methyl‐3‐indolylcarboxyamide)phenyl]acetyl] ‐(4S)‐methoxy‐(2S)‐pyrrolidinylmethoxy]cyclohexanecarboxylic Acid (V) via Reductive Etherification.

Cited by 0 publications

References 1 publication

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