Design of modular approach based Ku-band telemetry transmitter for geostationary satellites

2017 ◽  
Author(s):  
B S Himani ◽  
Khan Afzaal ◽  
K Sai Malleswar ◽  
Sirshendu Das ◽  
Rajeev Ranjan ◽  
...  
Keyword(s):  
Modular Approach ◽  
Geostationary Satellites ◽  
Telemetry Transmitter ◽  
Ku Band

Regular Observations of Geostationary Satellites by Combined CCD-Method

2004 ◽  
Vol 36 (9) ◽  
pp. 29-34
Author(s):  
Evgeniy S. Kozyrev ◽  
Evgeniya S. Sibiryakova ◽  
Alexander V. Shulga
Keyword(s):  
Geostationary Satellites

A Ku-band multibeam active phased array for satellite communications

1992 ◽  
Author(s):  
R. SORBELLO ◽  
A. ZAGHLOUL ◽  
R. GUPTA ◽  
B. GELLER ◽  
F.T. ASSAL
Keyword(s):  
Phased Array ◽  
Satellite Communications ◽  
Ku Band

A Revised Modular Approach to D8-THC and Derivatives Through Late-Stage Suzuki-Miyaura Cross-Coupling Reactions

2019 ◽  
Author(s):  
Victor Bloemendal ◽  
Floris P. J. T. Rutjes ◽  
Thomas J. Boltje ◽  
Daan Sondag ◽  
Hidde Elferink ◽  
...  
Keyword(s):  
Biological Activity ◽  
Late Stage ◽  
Medicinal Chemistry ◽  
Cross Coupling ◽  
Modular Approach ◽  
Coupling Reactions ◽  
One Pot ◽  
Biologically Relevant ◽  
Cross Coupling Reactions ◽  
Chemistry Research

<p>In this manuscript we describe a modular pathway to synthesize biologically relevant (–)-<i>trans</i>-Δ<sup>8</sup>-THC derivatives, which can be used to modulate the pharmacologically important CB<sub>1</sub> and CB<sub>2</sub> receptors. This pathway involves a one-pot Friedel-Crafts alkylation/cyclization protocol, followed by Suzuki-Miyaura cross-coupling reactions and gives rise to a series of new Δ<sup>8</sup>-THC derivatives. In addition, we demonstrate using extensive NMR evidence that similar halide-substituted Friedel-Crafts alkylation/cyclization products in previous articles were wrongly assigned as the para-isomers, which also has consequence for the assignment of the subsequent cross-coupled products and interpretation of their biological activity. </p> <p>Considering the importance of the availability of THC derivatives in medicinal chemistry research and the fact that previously synthesized compounds were wrongly assigned, we feel this research is describing a straightforward pathway into new cannabinoids.</p>

The Total Synthesis of Rhabdastrellic Acid A

2018 ◽  
Author(s):  
Yaroslav Boyko ◽  
Christopher Huck ◽  
David Sarlah
Keyword(s):  
Total Synthesis ◽  
Late Stage ◽  
Cross Coupling ◽  
Side Chains ◽  
General Strategy ◽  
Modular Approach ◽  
Linear Sequence ◽  
Generating Sequence ◽  
First Time

<div>The first total synthesis of rhabdastrellic acid A, a highly cytotoxic isomalabaricane triterpenoid, has been accomplished in a linear sequence of 14 steps from commercial geranylacetone. The prominently strained <i>trans-syn-trans</i>-perhydrobenz[<i>e</i>]indene core characteristic of the isomalabaricanes is efficiently accessed in a selective manner for the first time through a rapid, complexity-generating sequence incorporating a reductive radical polyene cyclization, an unprecedented oxidative Rautenstrauch cycloisomerization, and umpolung 𝛼-substitution of a <i>p</i>-toluenesulfonylhydrazone with in situ reductive transposition. A late-stage cross-coupling in concert with a modular approach to polyunsaturated side chains renders this a general strategy for the synthesis of numerous family members of these synthetically challenging and hitherto inaccessible marine triterpenoids.</div>

Split ring resonator inspired microstrip filtenna for Ku-band application

2017 ◽  
Vol 50 (4-6) ◽  
pp. 391-403 ◽  
Author(s):  
Soumya RANJAN MISHRA ◽  
K. L. SHEEJA ◽  
Nagendra P. PATHAK
Keyword(s):  
Ring Resonator ◽  
Split Ring Resonator ◽  
Split Ring ◽  
Ku Band
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