The use of J-coupling as a sole criterion to assign the total absolute stereochemistry of new pyrrolidinone class synthetic analogs, derived from S-pyroglutamic acid

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3026284 13 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
The use of J-coupling as a sole criterion to assign the total absolute stereochemistry of new pyrrolidinone class synthetic analogs, derived from S-pyroglutamic acid
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
During the synthesis of new pyrrolidinone analogs possessing biological activity it is intriguing to assign their absolute stereochemistry as it is well known that drug potency is influenced by the stereochemistry. The combination of J-coupling information with theoretical results was used in order to establish their total stereochemistry when the chiral center of the starting material has known absolute stereochemistry. The J-coupling can be used as a sole criterion for novel synthetic analogs to identify the right stereochemistry. This approach is extremely useful especially in the case of analogs whose 2D NOESY spectra cannot provide this information. Few synthetic examples are given to prove the significance of this approach. © 2016 Elsevier B.V.
Έτος δημοσίευσης:
2017
Συγγραφείς:
Kellici, T.F.
Ntountaniotis, D.
Vanioti, M.
Golic Grdadolnik, S.
Simcic, M.
Michas, G.
Moutevelis-Minakakis, P.
Mavromoustakos, T.
Περιοδικό:
Journal of Molecular Structure
Εκδότης:
Elsevier B.V.
Τόμος:
1129
Σελίδες:
195-199
Λέξεις-κλειδιά:
Bioactivity; Nuclear magnetic resonance spectroscopy; Organic compounds; Stereochemistry, Absolute stereochemistry; Chiral centers; J coupling; Pyroglutamic acids; Pyrrolidinone; Synthetic analogs, Stereoselectivity
Επίσημο URL (Εκδότης):
DOI:
10.1016/j.molstruc.2016.09.075
Το ψηφιακό υλικό του τεκμηρίου δεν είναι διαθέσιμο.