Divergent synthesis of N-hydroxy-L-indospicine, the carbon isostere ofN-hydroxy-L-arginine, and N-hydroxy-L-homoarginine from L-glutamate

Hiroyo Kabasawa; Makoto Yoshida; Tsutomu Ishikawa

Journal ArticleOPEN ACCESS

Divergent synthesis of N-hydroxy-L-indospicine, the carbon isostere ofN-hydroxy-L-arginine, and N-hydroxy-L-homoarginine from L-glutamate

Arkivoc (2003) 2003(8) 180-187

DOI: 10.3998/ark.5550190.0004.818

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Abstract

The carbon isostere of N-hydroxy-L-arginine, N-hydroxy-L-indospicine, and N-hydroxy-L-homoarginine, were prepared by divergent synthesis as possible NOS substrates, from L-glutamate.

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Kabasawa, H., Yoshida, M., & Ishikawa, T. (2003). Divergent synthesis of N-hydroxy-L-indospicine, the carbon isostere ofN-hydroxy-L-arginine, and N-hydroxy-L-homoarginine from L-glutamate. Arkivoc, 2003(8), 180–187. https://doi.org/10.3998/ark.5550190.0004.818

Divergent synthesis of N-hydroxy-L-indospicine, the carbon isostere ofN-hydroxy-L-arginine, and N-hydroxy-L-homoarginine from L-glutamate

Abstract

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