Convenient synthesis of a cyclic peptide disulfide: A type II β-turn structural model

Carlos García-Echeverría; Fernando Albericio; Miquel Pons; George Barany

doi:10.1016/S0040-4039(01)80422-6

Convenient synthesis of a cyclic peptide disulfide: A type II β-turn structural model

Carlos García-Echeverría
, Fernando Albericio
, Miquel Pons
, George Barany

Chemistry (Twin Cities)

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

34 Scopus citations

Abstract

Type II β-turn peptides can be stabilized by a disulfide bond. This bond is conveniently formed while the peptide remains attached to a polymeric support.

Original language	English (US)
Pages (from-to)	2441-2444
Number of pages	4
Journal	Tetrahedron Letters
Volume	30
Issue number	18
DOIs	https://doi.org/10.1016/S0040-4039(01)80422-6
State	Published - 1989

Bibliographical note

Funding Information:
Acknowledgments: This work was supported by funds from CICYT (BT 86-18), NIH CIRIT, US-Spain Joint Committee for Scientific and Technological Cooperation, (Collaborative Research Grant 0841/88).

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10.1016/S0040-4039(01)80422-6

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@article{0750dbc9ef974895ba0d9fb3f9c21b0c,

title = "Convenient synthesis of a cyclic peptide disulfide: A type II β-turn structural model",

abstract = "Type II β-turn peptides can be stabilized by a disulfide bond. This bond is conveniently formed while the peptide remains attached to a polymeric support.",

author = "Carlos Garc{\'i}a-Echeverr{\'i}a and Fernando Albericio and Miquel Pons and George Barany",

note = "Funding Information: Acknowledgments: This work was supported by funds from CICYT (BT 86-18), NIH CIRIT, US-Spain Joint Committee for Scientific and Technological Cooperation, (Collaborative Research Grant 0841/88).",

year = "1989",

doi = "10.1016/S0040-4039(01)80422-6",

language = "English (US)",

volume = "30",

pages = "2441--2444",

journal = "Tetrahedron Letters",

issn = "0040-4039",

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T1 - Convenient synthesis of a cyclic peptide disulfide

T2 - A type II β-turn structural model

AU - García-Echeverría, Carlos

AU - Albericio, Fernando

AU - Pons, Miquel

AU - Barany, George

N1 - Funding Information: Acknowledgments: This work was supported by funds from CICYT (BT 86-18), NIH CIRIT, US-Spain Joint Committee for Scientific and Technological Cooperation, (Collaborative Research Grant 0841/88).

PY - 1989

Y1 - 1989

N2 - Type II β-turn peptides can be stabilized by a disulfide bond. This bond is conveniently formed while the peptide remains attached to a polymeric support.

AB - Type II β-turn peptides can be stabilized by a disulfide bond. This bond is conveniently formed while the peptide remains attached to a polymeric support.

UR - https://www.scopus.com/pages/publications/0000836350

UR - https://www.scopus.com/pages/publications/0000836350#tab=citedBy

U2 - 10.1016/S0040-4039(01)80422-6

DO - 10.1016/S0040-4039(01)80422-6

M3 - Article

AN - SCOPUS:0000836350

SN - 0040-4039

VL - 30

SP - 2441

EP - 2444

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 18

ER -

Convenient synthesis of a cyclic peptide disulfide: A type II β-turn structural model

Abstract

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