Linear Positional Isomer Sorting in Nonporous Adaptive Crystals of a Pillar[5]arene

2018 ◽  
Vol 140 (9) ◽  
pp. 3190-3193 ◽  
Author(s):  
Kecheng Jie ◽  
Yujuan Zhou ◽  
Errui Li ◽  
Run Zhao ◽  
Ming Liu ◽  
...  
Keyword(s):  
1989 ◽  
Vol 42 (11) ◽  
pp. 1983 ◽  
Author(s):  
JC Coll ◽  
AD Wright

Four collections of the red algae Chondrococcus hornemannii( Lyngbye ) Schmitz afforded a range of monoterpenes. Structures of ten new metabolites were elucidated by using high- field n.m.r. spectroscopy techniques including 2.D proton-carbon correlation experiments. The new monoterpenes were: (Z)-3-bromo-8-chloro-6-chloromethyl-2-methylocta-1,6-diene (9,6-hydroxymethyl-2-methylocta-2,8-dien-6-ol (6), (Z)-6-hydroxymethyl-2-methylocta-1,6-diene- 3,8-diol (7), (2)-6-hydroxymethyl-2-methyIocta-2,6-dien-8-ol (8), (2)-8-chloro-6-chloromethyl-3- methoxyocta-1,6-diene (9), (Z)-8-chloso-6-chloromethyl-2-methylocta-l,6-dien-3-ol (10), (2E,62) 8-chloro-6-chloromethyl-1-methoxy-2-methylocta-2,6-diene (11), (2E,6Z)-8-chloro-6-chloromethyl- 2-methylocta-2,6-dien-1-ol (12), (Z)-6-chloromethyl-3,8-dimethoxy-2-methylocta-1,6-diene (13) and its positional isomer (Z)-6-chloromethyl-1,8-dimethoxy-2-methyoca-26-diene (14). Although it is possible that some of the metabolites listed may be artefacts of extraction, circumstantial evidence is offered which suggests that most isolates were present in the plant prior to extraction.


1975 ◽  
Vol 64 (6) ◽  
pp. 1047 ◽  
Author(s):  
Thomas J. Schwan ◽  
K.O. Ellis

1999 ◽  
Vol 315 (3-4) ◽  
pp. 251-261 ◽  
Author(s):  
Wei Zou ◽  
Jean-Robert Brisson ◽  
Suzon Larocque ◽  
Rebecca L. Gardner ◽  
Harold J. Jennings

Sign in / Sign up

Export Citation Format

Share Document