Preparation of Spirocyclic β-Proline Esters: Geometrically Restricted Building Blocks for Medicinal Chemistry
Publikation: Bidrag til tidsskrift › Review › Forskning › fagfællebedømt
Standard
Preparation of Spirocyclic β-Proline Esters : Geometrically Restricted Building Blocks for Medicinal Chemistry. / Fjelbye, Kasper; Marigo, Mauro; Clausen, Rasmus Prætorius; Juhl, Karsten.
I: SYNLETT: Accounts and Rapid Communications in Chemical Synthesis, Bind 28, Nr. 2, st-2016-b0534-l, 2017, s. 231-234.Publikation: Bidrag til tidsskrift › Review › Forskning › fagfællebedømt
Harvard
APA
Vancouver
Author
Bibtex
}
RIS
TY - JOUR
T1 - Preparation of Spirocyclic β-Proline Esters
T2 - Geometrically Restricted Building Blocks for Medicinal Chemistry
AU - Fjelbye, Kasper
AU - Marigo, Mauro
AU - Clausen, Rasmus Prætorius
AU - Juhl, Karsten
PY - 2017
Y1 - 2017
N2 - A series of novel N-Bn-protected spirocyclic β-proline esters were prepared using [3+2] cycloaddition and subsequently converted into their corresponding aldehydes. In addition, two novel N-Cbz-protected spirocyclic β-proline esters were prepared using intramolecular cyclization starting from simple precursors.
AB - A series of novel N-Bn-protected spirocyclic β-proline esters were prepared using [3+2] cycloaddition and subsequently converted into their corresponding aldehydes. In addition, two novel N-Cbz-protected spirocyclic β-proline esters were prepared using intramolecular cyclization starting from simple precursors.
KW - 1,3-dipolar cycloaddition
KW - intramolecular cyclization
KW - oxetanes
KW - spirocycles
KW - β-proline esters
U2 - 10.1055/s-0036-1588902
DO - 10.1055/s-0036-1588902
M3 - Review
AN - SCOPUS:84991735346
VL - 28
SP - 231
EP - 234
JO - SYNLETT: Accounts and Rapid Communications in Chemical Synthesis
JF - SYNLETT: Accounts and Rapid Communications in Chemical Synthesis
SN - 0936-5214
IS - 2
M1 - st-2016-b0534-l
ER -
ID: 176009623