ChemInform Abstract: A New Method for Peptide Synthesis in the N→C Direction: Amide Assembly Through Silver-Promoted Reaction of Thioamides.

Aysa Pourvali; James R. Cochrane; Craig A. Hutton

doi:10.1002/chin.201517259

ChemInform Abstract: A New Method for Peptide Synthesis in the N→C Direction: Amide Assembly Through Silver-Promoted Reaction of Thioamides.

ChemInform ◽

10.1002/chin.201517259 ◽

2015 ◽

Vol 46 (17) ◽

pp. no-no

Author(s):

Aysa Pourvali ◽

James R. Cochrane ◽

Craig A. Hutton

Keyword(s):

Peptide Synthesis ◽

New Method

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A NEW METHOD FOR PEPTIDE SYNTHESIS USINGo-NITROPHENYLSULFENYLN-CARBOXY α-AMINO ACID ANHYDRIDES

Chemistry Letters ◽

10.1246/cl.1974.1529 ◽

1974 ◽

Vol 3 (12) ◽

pp. 1529-1530 ◽

Cited By ~ 4

Author(s):

Ryoichi Katakai ◽

Masanao Oya

Keyword(s):

Amino Acid ◽

Peptide Synthesis ◽

New Method ◽

Acid Anhydrides

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New approach to the use of 2-bromoethyl esters in peptide synthesis

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19882787 ◽

1988 ◽

Vol 53 (11) ◽

pp. 2787-2790 ◽

Cited By ~ 1

Author(s):

M. Joaquina S. A. Amaral Trigo ◽

M. Isabel A. Oliveira Santos

Keyword(s):

Peptide Synthesis ◽

Room Temperature ◽

New Method ◽

New Approach

The synthesis of six new fully protected dipeptides 2-bromoethyl esters and a new method for the removal of the C-protection by the action of the sulphide anion, at room temperature, are described.

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A New Method for the Detection of Racemization during Peptide Synthesis: Stereoselective hydrolysis of diastereomeric peptides by leucine aminopeptidase

Helvetica Chimica Acta ◽

10.1002/hlca.19730560216 ◽

1973 ◽

Vol 56 (2) ◽

pp. 717-723 ◽

Cited By ~ 23

Author(s):

Hans Rudolf Bonsshard ◽

Israel Schechter ◽

Arieh Berger

Keyword(s):

Peptide Synthesis ◽

Leucine Aminopeptidase ◽

New Method ◽

Stereoselective Hydrolysis ◽

Hydrolysis Of

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ChemInform Abstract: A NEW METHOD FOR PEPTIDE SYNTHESIS USING O-NITRO-PHENYLSULFENYL N-CARBOXY ALPHA-AMINO ACID ANHYDRIDES

Chemischer Informationsdienst ◽

10.1002/chin.197545430 ◽

1975 ◽

Vol 6 (45) ◽

pp. no-no

Author(s):

R. KATAKAI ◽

M. OYA

Keyword(s):

Amino Acid ◽

Peptide Synthesis ◽

New Method ◽

Acid Anhydrides ◽

Alpha Amino Acid

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A new method for peptide synthesis by oxidation-reduction condensation

Journal of the American Chemical Society ◽

10.1021/ja01018a072 ◽

1968 ◽

Vol 90 (16) ◽

pp. 4490-4491 ◽

Cited By ~ 33

Author(s):

Teruaki. Mukaiyama ◽

Masaaki. Ueki ◽

Hiroshi. Maruyama ◽

Rei. Matsueda

Keyword(s):

Peptide Synthesis ◽

New Method ◽

Oxidation Reduction

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A new method for peptide synthesis in the N→C direction: amide assembly through silver-promoted reaction of thioamides

Chemical Communications ◽

10.1039/c4cc07601j ◽

2014 ◽

Vol 50 (100) ◽

pp. 15963-15966 ◽

Cited By ~ 18

Author(s):

Aysa Pourvali ◽

James R. Cochrane ◽

Craig A. Hutton

Keyword(s):

Peptide Synthesis ◽

New Method ◽

Peptide Acids

The Ag(i)-promoted coupling of peptide-acids with thioamides generates peptide-imides, which was exploited in the synthesis of peptides in the N→C direction.

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