FN Archimer Export Format
PT J
TI Marine Natural Occurring 2,5-Diketopiperazines: Isolation, Synthesis and Optical Properties
BT 
AF LAVILLE, Remi
   MORIOU, Celine
   PETEK, Sylvain
   DEBITUS, Cecile
   AL-MOURABIT, Ali
AS 1:1;2:1;3:1;4:2;5:2;6:1;
FF 1:;2:;3:;4:;5:;6:;
C1 CNRS, Inst Chim Subst Nat, Ctr Rech Gif Sur Yvette, F-91198 Gif Sur Yvette, France.
   Ctr Polynesie Francaise, IRD, UMR241, Papeete, France.
C2 CNRS, FRANCE
   IRD, FRANCE
UM EIO
IF 1.107
TC 11
UR https://archimer.ifremer.fr/doc/00667/77944/82136.pdf
LA English
DT Article
DE ;Diketopiperazine;Sponge;Marine Metabolite;Circular Dichroism
AB Seven 2,5-diketopiperazines (DKPs) were isolated from the Fijian marine sponge Acanthella cavernosa. NMR and circular dichroism (CD) comparison with synthetic L-L DKPs allowed us to determine unambiguously the L-L absolute configuration of the natural DKPs. This work initiated the setting up of an optical properties database of natural DKPs, including specific rotation and CD. 
PY 2015
PD JAN
SO Heterocycles
SN 0385-5414
PU Pergamon-elsevier Science Ltd
VL 90
IS 2
UT 000349505900048
BP 1351
EP 1366
DI 10.3987/COM-14-S(K)87
ID 77944
ER

EF