Nucleophile-mediated oxa-Michael addition reactions of divinyl sulfone - a thiol-free option for step-growth polymerisations

Research output: Contribution to journal › Article

Original language	English
Pages (from-to)	5091-5094
Journal	Catalysis Science & Technology
Volume	5
DOIs	https://doi.org/10.1039/c5cy01527h
Publication status	Published - 2015

Treatment code (Nähere Zuordnung)

@article{f7b52ee74bfb4cefaedd180c629cfae5,

title = "Nucleophile-mediated oxa-Michael addition reactions of divinyl sulfone - a thiol-free option for step-growth polymerisations",

author = "Simone Strasser and Christian Slugovc",

year = "2015",

doi = "10.1039/c5cy01527h",

language = "English",

volume = "5",

pages = "5091--5094",

journal = "Catalysis Science & Technology",

issn = "2044-4761 ",

publisher = "Royal Society of Chemistry",

}

TY - JOUR

T1 - Nucleophile-mediated oxa-Michael addition reactions of divinyl sulfone - a thiol-free option for step-growth polymerisations

AU - Strasser, Simone

AU - Slugovc, Christian

PY - 2015

Y1 - 2015

U2 - 10.1039/c5cy01527h

DO - 10.1039/c5cy01527h

M3 - Article

SN - 2044-4761

VL - 5

SP - 5091

EP - 5094

JO - Catalysis Science & Technology

JF - Catalysis Science & Technology

ER -