Racemization-free synthesis of S-alkylated cysteines via thiol-ene reaction

G. Triola; L. Brunsveld; H. Waldmann

doi:10.1021/jo800198s

Racemization-free synthesis of S-alkylated cysteines via thiol-ene reaction

G. Triola, L. Brunsveld, H. Waldmann

Chemical Biology

Onderzoeksoutput: Bijdrage aan tijdschrift › Tijdschriftartikel › Academic › peer review

57 Citaten (Scopus)

Samenvatting

Treatment of differently protected and unprotected cysteines with a variety of alkenes in the presence of a radical initiator (AIBN) afforded the corresponding S-alkylated cysteines in high yields and without racemization.

Originele taal-2	Engels
Pagina's (van-tot)	3646-3649
Tijdschrift	Journal of Organic Chemistry
Volume	73
Nummer van het tijdschrift	9
DOI's	https://doi.org/10.1021/jo800198s
Status	Gepubliceerd - 2008

Toegang tot document

10.1021/jo800198s

Citeer dit

@article{0e5e99756be24b56b67abdbca6b26f6f,

title = "Racemization-free synthesis of S-alkylated cysteines via thiol-ene reaction",

abstract = "Treatment of differently protected and unprotected cysteines with a variety of alkenes in the presence of a radical initiator (AIBN) afforded the corresponding S-alkylated cysteines in high yields and without racemization.",

author = "G. Triola and L. Brunsveld and H. Waldmann",

year = "2008",

doi = "10.1021/jo800198s",

language = "English",

volume = "73",

pages = "3646--3649",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "9",

}

TY - JOUR

T1 - Racemization-free synthesis of S-alkylated cysteines via thiol-ene reaction

AU - Triola, G.

AU - Brunsveld, L.

AU - Waldmann, H.

PY - 2008

Y1 - 2008

N2 - Treatment of differently protected and unprotected cysteines with a variety of alkenes in the presence of a radical initiator (AIBN) afforded the corresponding S-alkylated cysteines in high yields and without racemization.

AB - Treatment of differently protected and unprotected cysteines with a variety of alkenes in the presence of a radical initiator (AIBN) afforded the corresponding S-alkylated cysteines in high yields and without racemization.

U2 - 10.1021/jo800198s

DO - 10.1021/jo800198s

M3 - Article

C2 - 18376863

SN - 0022-3263

VL - 73

SP - 3646

EP - 3649

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 9

ER -

Racemization-free synthesis of S-alkylated cysteines via thiol-ene reaction

Samenvatting

Toegang tot document

Vingerafdruk

Citeer dit