<i>N</i>-Allyl-<i>N</i>-(2-nitrobenzenesulfonyl)-<scp>L</scp>-leucine methyl ester

Laurent F. Bornaghi; Sally‐Ann Poulsen; Peter C. Healy

doi:10.1107/s1600536804003186

ScienceGate Book Chapters

JOURNAL ARTICLE

N-Allyl-N-(2-nitrobenzenesulfonyl)-L-leucine methyl ester

Laurent F. Bornaghi Sally‐Ann Poulsen Peter C. Healy

Year: 2004 Journal: Acta Crystallographica Section E Structure Reports Online Vol: 60 (3)Pages: o383-o385 Publisher: International Union of Crystallography

DOI: 10.1107/s1600536804003186

Get Full-Text PDF Get Analytical Report

Abstract

The structure of the title compound, C16H22N2O6S, has been determined as part of an ongoing investigation into the preparation of N-alkylated amino acid precursors for alkene cross-metathesis reactions for the generation of dynamic combinatorial libraries. The overall molecular conformation is stabilized by intramolecular C-HO interactions.

Keywords:

Alkene Intramolecular force Chemistry Metathesis Leucine Stereochemistry Salt metathesis reaction Alkyl Amino acid Medicinal chemistry Organic chemistry Biochemistry Catalysis Polymerization

Metrics

Cited By

0.22

FWCI (Field Weighted Citation Impact)

Refs

0.51

Citation Normalized Percentile

Is in top 1%

Is in top 10%

Topics

Synthetic Organic Chemistry Methods

Physical Sciences → Chemistry → Organic Chemistry

Chemical Synthesis and Analysis

Life Sciences → Biochemistry, Genetics and Molecular Biology → Molecular Biology

Synthesis and Catalytic Reactions

Physical Sciences → Chemistry → Organic Chemistry

N-Allyl-N-(2-nitrobenzenesulfonyl)-L-leucine methyl ester

Abstract

Metrics

Topics

Related Documents

N-Allyl-N-(2-nitrobenzenesulfonyl)-L-phenylalanine methyl ester

N-(2-Nitrobenzenesulfonyl)-L-alanine methyl ester

N-(2-Carboxybenzoyl)-L-leucine methyl ester

N-{N-[N-(1,1-Dimethylethoxycarbonyl)-L-leucyl]-N-methyl-L-leucyl}-N-methyl-L-leucine benzyl ester

N-Cinnamoyl-L-valine methyl ester