X-ray probing of high field ionization in the attosecond limit

Author(s):  
Stephen R. Leone
Keyword(s):  
2021 ◽  
Vol 104 (6) ◽  
Author(s):  
Sh. Yamamoto ◽  
D. I. Gorbunov ◽  
I. F. Diaz-Ortega ◽  
A. Miyata ◽  
T. Kihara ◽  
...  
Keyword(s):  
X Ray ◽  

2017 ◽  
Vol 7 (7) ◽  
pp. 671 ◽  
Author(s):  
Toshiaki Inada ◽  
Takayuki Yamazaki ◽  
Tomohiro Yamaji ◽  
Yudai Seino ◽  
Xing Fan ◽  
...  

1997 ◽  
Vol 56 (6) ◽  
pp. 5183-5186 ◽  
Author(s):  
K. Nagashima ◽  
T. Matoba ◽  
H. Takuma

2006 ◽  
Vol 75 (2) ◽  
pp. 024710 ◽  
Author(s):  
Y. H. Matsuda ◽  
T. Inami ◽  
K. Ohwada ◽  
Y. Murata ◽  
H. Nojiri ◽  
...  

Author(s):  
M.-C. Chou ◽  
T.-S. Hung ◽  
J.-Y. Lin ◽  
P.-H. Lin ◽  
S.-Y. Chen ◽  
...  
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1987 ◽  
Vol 335 (2) ◽  
pp. 213-227 ◽  
Author(s):  
Bavani Mailvaganam ◽  
Brian E. McCarry ◽  
Brian G. Sayer ◽  
Richard E. Perrier ◽  
Romolo Faggiani ◽  
...  
Keyword(s):  

2001 ◽  
Author(s):  
Katsuya Oguri ◽  
Hidetoshi Nakano ◽  
Tadashi Nishikawa ◽  
Naoshi Uesugi

1983 ◽  
Vol 36 (11) ◽  
pp. 2279 ◽  
Author(s):  
BF Bowden ◽  
JC Coll ◽  
VA Patrick ◽  
DM Tapiolas

Three new diterpenes have been isolated from soft corals of the genus Efflatounaria (Coelenterata, Octocorallia, Alcyonacea, Xeniidae). The structure of the first compound (4) was elucidated on the basis of high-field 1H n.m.r. spectroscopy while that of the second metabolite (5) was determined by single-crystal X-ray analysis. The third diterpene (6) was structurally related to (5), and its structure was confirmed by chemical transformation. All three diterpenes can be derived from xenicin-type precursors, by cleavage and recyclization.


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