Biosynthesis of the Pipecolate Moiety of Marcfortine A-Reference-Cited by-同舟云学术

Biosynthesis of the Pipecolate Moiety of Marcfortine A

Published:1999-02-23 Issue:9 Volume:121 Page:1763-1767
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Kuo M. S.¹,Yurek D. A.¹,Mizsak S. A.¹,Cialdella J. I.¹,Baczynskyj L.¹,Marshall V. P.¹

Affiliation:

1. Contribution from Discovery Technologies, Structural, Analytical and Medicinal Chemistry and Protein Biochemistry. Pharmacia and Upjohn Company, Kalamazoo, Michigan 49001

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja983128d

Reference19 articles.

1. See: Evans, J. N.Biomolecular NMR Spectroscopy; Oxford Press: New York, 1995; pp 256−265. Breitmaier, E.; Voeiter, W.Carbon-13 NMRSpectrosopy, High-Resolution Methods and Applications in OrganicChemistry and Biochemistry, 3rd ed.; VCH: New York, 1987; pp 451−459.

2. See: Levy, G.; Lichter, R. L.Nitrogen-15 Nuclear MagneticResonance Spectroscopy; John Wiley & Sons: New York, 1979; pp 2−28. Witanowski, M.; Stefaniak, M.; Webb, G. A.Ann. Rep. NMR Spectrosc.1993,25, 15−16.

3. Synthesis of alternating hydroxy- and methyl-substituted hydrocarbons by oxymercuration of cyclopropylcarbinols

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