Gas-Phase Infrared Spectroscopy for Determination of Double Bond Configuration of Monounsaturated Compounds

1994 ◽  
Vol 66 (10) ◽  
pp. 1696-1703 ◽  
Author(s):  
Athula B. Attygalle ◽  
Ales. Svatos ◽  
Charles. Wilcox ◽  
Simon. Voerman
Keyword(s):  
Infrared Spectroscopy ◽  
Double Bond ◽  
Gas Phase

Gas-Phase Infrared Spectroscopy for Determination of Double-Bond Configuration of Some Polyunsaturated Pheromones and Related Compounds

1995 ◽  
Vol 67 (9) ◽  
pp. 1558-1567 ◽  
Author(s):  
Athula B. Attygalle ◽  
Ales. Svatos ◽  
Charles. Wilcox ◽  
Simon. Voerman
Keyword(s):  
Infrared Spectroscopy ◽  
Double Bond ◽  
Gas Phase ◽  
Related Compounds

scholarly journals Determination of Noncovalent Docking by Infrared Spectroscopy of Cold Gas-Phase Complexes

Science ◽  
2012 ◽  
Vol 335 (6069) ◽  
pp. 694-698 ◽  
Author(s):  
E. Garand ◽  
M. Z. Kamrath ◽  
P. A. Jordan ◽  
A. B. Wolk ◽  
C. M. Leavitt ◽  
...  
Keyword(s):  
Infrared Spectroscopy ◽  
Gas Phase ◽  
Cold Gas

Structure Determination of Gas-Phase Niobium and Tantalum Carbide Nanocrystals via Infrared Spectroscopy

2002 ◽  
Vol 89 (1) ◽  
Author(s):  
Deniz van Heijnsbergen ◽  
André Fielicke ◽  
Gerard Meijer ◽  
Gert von Helden
Keyword(s):  
Infrared Spectroscopy ◽  
Gas Phase ◽  
Structure Determination ◽  
Tantalum Carbide

Infrared Spectroscopy of Gas-Phase Cr+Coordination Complexes:  Determination of Binding Sites and Electronic States

2005 ◽  
Vol 127 (19) ◽  
pp. 7243-7254 ◽  
Author(s):  
David T. Moore ◽  
Jos Oomens ◽  
John R. Eyler ◽  
Gert von Helden ◽  
Gerard Meijer ◽  
...  
Keyword(s):  
Infrared Spectroscopy ◽  
Gas Phase ◽  
Binding Sites ◽  
Electronic States ◽  
Coordination Complexes

THE THYMOLYTIC ACTIVITY OF 6- AND 9-HALOCORTICOIDS AND RELATED STEROIDS

1965 ◽  
Vol 49 (2) ◽  
pp. 262-270 ◽  
Author(s):  
Ralph I. Dorfman ◽  
P. G. Holton ◽  
Fred A. Kind
Keyword(s):  
Double Bond ◽  
Subcutaneous Injection ◽  
Fluocinolone Acetonide ◽  
Relative Potency ◽  
Subcutaneous Route ◽  
Adrenalectomized Rats

ABSTRACT Adrenalectomized rats were used for the determination of the relative potency of various 6- and 9-halo substituted corticoids administered subcutaneously or by gavage using thymus weightas the endpoint. By subcutaneous injection, fluocinolone acetonide was the most active corticoid at 700 times that of cortisol. This compound was also the most active corticoid by the gavage route and was judged to be 570 times as active as the standard cortisol. The introduction of the 16,17-acetonide and 16,17-acetone 21-acetate groups into 17α,21-dihydroxy-9α,11β-dichloropregna-1,4-diene-3,20-dione increased the activity by a factor of 42 and 100, respectively. The introduction of the δ1 double bond into 6α-fluoroprogesterone 16,17-acetonide caused an increase of 10-fold in thymolytic activity assessed by the subcutaneous route

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