Preparation and determination of X-ray-crystal and NMR-solution structures of γ2,3,4-peptides

D. Seebach; M. Brenner; M. Rueping; B. Schweizer; B. Jaun

doi:10.1039/b008377l

Preparation and determination of X-ray-crystal and NMR-solution structures of γ^2,3,4-peptides

D. Seebach^*, M. Brenner, M. Rueping, B. Schweizer, B. Jaun

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

109 Scopus citations

Abstract

(R,R,R)-γ-Amino acids with side chains in the 2-, 3-, and 4-positions, prepared by addition of acyloxazolidinones to a nitroolefin and hydrogenation, have been coupled to γ-tetra-, and γ-hexapeptides which are shown to form (M)-2.6₁₄ helices in the crystal state and in MeOH solution.

Original language	English (US)
Pages (from-to)	207-208
Number of pages	2
Journal	CHEMICAL COMMUNICATIONS
Issue number	2
DOIs	https://doi.org/10.1039/b008377l
State	Published - Jan 21 2001
Externally published	Yes

ASJC Scopus subject areas

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
General Chemistry
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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title = "Preparation and determination of X-ray-crystal and NMR-solution structures of γ2,3,4-peptides",

abstract = "(R,R,R)-γ-Amino acids with side chains in the 2-, 3-, and 4-positions, prepared by addition of acyloxazolidinones to a nitroolefin and hydrogenation, have been coupled to γ-tetra-, and γ-hexapeptides which are shown to form (M)-2.614 helices in the crystal state and in MeOH solution.",

author = "D. Seebach and M. Brenner and M. Rueping and B. Schweizer and B. Jaun",

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T1 - Preparation and determination of X-ray-crystal and NMR-solution structures of γ2,3,4-peptides

AU - Seebach, D.

AU - Brenner, M.

AU - Rueping, M.

AU - Schweizer, B.

AU - Jaun, B.

PY - 2001/1/21

Y1 - 2001/1/21

N2 - (R,R,R)-γ-Amino acids with side chains in the 2-, 3-, and 4-positions, prepared by addition of acyloxazolidinones to a nitroolefin and hydrogenation, have been coupled to γ-tetra-, and γ-hexapeptides which are shown to form (M)-2.614 helices in the crystal state and in MeOH solution.

AB - (R,R,R)-γ-Amino acids with side chains in the 2-, 3-, and 4-positions, prepared by addition of acyloxazolidinones to a nitroolefin and hydrogenation, have been coupled to γ-tetra-, and γ-hexapeptides which are shown to form (M)-2.614 helices in the crystal state and in MeOH solution.

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U2 - 10.1039/b008377l

DO - 10.1039/b008377l

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JO - CHEMICAL COMMUNICATIONS

JF - CHEMICAL COMMUNICATIONS

IS - 2

ER -

Preparation and determination of X-ray-crystal and NMR-solution structures of γ^2,3,4-peptides

Abstract

ASJC Scopus subject areas

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