Self‐Promoted Stereoselective Glycosylations – Past, Present, Future

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Self‐Promoted Stereoselective Glycosylations – Past, Present, Future. / Videcrantz Faurschou, Natasha; Marcus Pedersen, Christian.

I: The Chemical Record, Bind 21, Nr. 11, 2021, s. 3063-3075.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Videcrantz Faurschou, N & Marcus Pedersen, C 2021, 'Self‐Promoted Stereoselective Glycosylations – Past, Present, Future', The Chemical Record, bind 21, nr. 11, s. 3063-3075. https://doi.org/10.1002/tcr.202100092

APA

Videcrantz Faurschou, N., & Marcus Pedersen, C. (2021). Self‐Promoted Stereoselective Glycosylations – Past, Present, Future. The Chemical Record, 21(11), 3063-3075. https://doi.org/10.1002/tcr.202100092

Vancouver

Videcrantz Faurschou N, Marcus Pedersen C. Self‐Promoted Stereoselective Glycosylations – Past, Present, Future. The Chemical Record. 2021;21(11):3063-3075. https://doi.org/10.1002/tcr.202100092

Author

Videcrantz Faurschou, Natasha ; Marcus Pedersen, Christian. / Self‐Promoted Stereoselective Glycosylations – Past, Present, Future. I: The Chemical Record. 2021 ; Bind 21, Nr. 11. s. 3063-3075.

Bibtex

@article{e4c2389cba1347c3b2d64bf229e14267,
title = "Self‐Promoted Stereoselective Glycosylations – Past, Present, Future",
abstract = "Self-promoted glycosylations have generally not received much attention, despite having the advantages of being easy to perform and often highly stereoselective. This account covers the work done in this field and the mechanistic aspects of self-promoted glycosylations are discussed, with a main focus on the stereoselectivity of the reactions. Most self-promoted glycosylations utilize trichloroacetimidate donors, but examples of self-promoted reactions with other donors have been described and will be discussed. Self-promoted glycosylation strategies can provide a basis for new stereoselective glycosylation methodologies.",
author = "{Videcrantz Faurschou}, Natasha and {Marcus Pedersen}, Christian",
note = "Dedicated to Professor Mikael Bols on the occasion of his 60th birthday.",
year = "2021",
doi = "10.1002/tcr.202100092",
language = "English",
volume = "21",
pages = "3063--3075",
journal = "Chemical Record",
issn = "1527-8999",
publisher = "Wiley - V C H Verlag GmbH & Co. KGaA",
number = "11",

}

RIS

TY - JOUR

T1 - Self‐Promoted Stereoselective Glycosylations – Past, Present, Future

AU - Videcrantz Faurschou, Natasha

AU - Marcus Pedersen, Christian

N1 - Dedicated to Professor Mikael Bols on the occasion of his 60th birthday.

PY - 2021

Y1 - 2021

N2 - Self-promoted glycosylations have generally not received much attention, despite having the advantages of being easy to perform and often highly stereoselective. This account covers the work done in this field and the mechanistic aspects of self-promoted glycosylations are discussed, with a main focus on the stereoselectivity of the reactions. Most self-promoted glycosylations utilize trichloroacetimidate donors, but examples of self-promoted reactions with other donors have been described and will be discussed. Self-promoted glycosylation strategies can provide a basis for new stereoselective glycosylation methodologies.

AB - Self-promoted glycosylations have generally not received much attention, despite having the advantages of being easy to perform and often highly stereoselective. This account covers the work done in this field and the mechanistic aspects of self-promoted glycosylations are discussed, with a main focus on the stereoselectivity of the reactions. Most self-promoted glycosylations utilize trichloroacetimidate donors, but examples of self-promoted reactions with other donors have been described and will be discussed. Self-promoted glycosylation strategies can provide a basis for new stereoselective glycosylation methodologies.

U2 - 10.1002/tcr.202100092

DO - 10.1002/tcr.202100092

M3 - Journal article

C2 - 34028947

VL - 21

SP - 3063

EP - 3075

JO - Chemical Record

JF - Chemical Record

SN - 1527-8999

IS - 11

ER -

ID: 269910574