Yngve Stenstrøm

Prof. Yngve Stenstrøm

orcid

Research Focus & Metrics

Academic Career Length

34Years (1993-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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24 October 2007 in The Journal of Physical Chemistry A
Verified
Journal Article
Closed access
AGAline Gratien
Aline Gratien
Elna NilssonElna Nilsson
Elna Nilsson
JDJean-Francois Doussin
Jean-Francois Doussin
Matthew Stanley JohnsonMatthew Stanley Johnson
Matthew Stanley Johnson
CNClaus J. Nielsen
Claus J. Nielsen
BPBénédicte Picquet-Varrault
Bénédicte Picquet-Varrault

21 May 2005 in The Journal of Physical Chemistry A
Verified
Journal Article
Closed access
BDBarbara D'Anna
Barbara D'Anna
AWArmin Wisthaler
Armin Wisthaler
ØAØyvind Andreasen
Øyvind Andreasen
AHArmin Hansel
Armin Hansel
JHJens Hjorth
Jens Hjorth
JVJyrki Viidanoja
Jyrki Viidanoja

1 February 2005 in Carbohydrate Research
Verified
Journal Article
Closed access
Dag EkebergDag Ekeberg
Dag Ekeberg
SMSvein Morgenlie
Svein Morgenlie
YSYngve Stenstrøm
Yngve Stenstrøm

1 January 2014 in Tetrahedron Letters
Verified
Journal Article
Closed access
LFLiudmila Filippova
Liudmila Filippova
YSYngve Stenstrøm
Yngve Stenstrøm
THTrond Vidar Hansen
Trond Vidar Hansen

1 January 1993 in Acta Chemica Scandinavica
Verified
Journal Article
Open access
LELars Eklund
Lars Eklund
AAAnna-Karin Axelsson
Anna-Karin Axelsson
ÅNÅke Nordahl
Åke Nordahl
RCRolf Carlson
Rolf Carlson
HMHarald Møllendal
Harald Møllendal
TTTadashi Tsuda
Tadashi Tsuda

9 April 2015 in Molecules
Verified
Journal Article
Open access
PDF file
LFLiudmila Filippova
Liudmila Filippova
YSYngve Stenstrøm
Yngve Stenstrøm
Trond Vidar HansenTrond Vidar Hansen
Trond Vidar Hansen
A novel C1-symmetric dinitrogen ligand was synthesized in high yield from commercially available (1R,2R,3R,5S)-(−)-isopinocampheylamine and 1-methyl-2-imidazolecarboxaldehyde. In combination with Cu(OAc)2H2O, this new ligand promote the reaction between nitromethane and aliphatic aldehydes with high yields (up to 97%) and moderate enantioselectivities (up to 67% ee). The reactions with benzaldehyde required prolonged reaction time that resulted in diminished yields, but accompanied with ee-values in the 55%–76% range.