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[011] waveguide stripe direction n-i-p-n heterostructure InP optical modulator
[011] waveguide stripe direction n-i-p-n heterostructure InP optical modulator
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[011] waveguide stripe direction n-i-p-n heterostructure InP optical modulator

Ogiso, Y ; Ohiso, Y ; Shibata, Y ; Kohtoku, M

Electronics letters, 2014-04, Vol.50 (9), p.688-690 [Periódico revisado por pares]

Stevenage: The Institution of Engineering and Technology

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2
0.5-V bulk-driven CMOS operational amplifier
0.5-V bulk-driven CMOS operational amplifier
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0.5-V bulk-driven CMOS operational amplifier

Kulej, Tomasz

IET circuits, devices & systems, 2013-11, Vol.7 (6), p.352-360 [Periódico revisado por pares]

Stevenage: The Institution of Engineering and Technology

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3
0.5 V inverter-based ultra-low-power, low-noise VGA for medical ultrasound probes
0.5 V inverter-based ultra-low-power, low-noise VGA for medical ultrasound probes
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0.5 V inverter-based ultra-low-power, low-noise VGA for medical ultrasound probes

Wang, P ; Halvorsrød, T.M ; Ytterdal, T

Electronics letters, 2014-01, Vol.50 (2), p.69-71 [Periódico revisado por pares]

Stevenage: The Institution of Engineering and Technology

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4
0.9–10.6 GHz UWB mixer using current bleeding for multi-band application
0.9–10.6 GHz UWB mixer using current bleeding for multi-band application
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0.9–10.6 GHz UWB mixer using current bleeding for multi-band application

Yeh, Chin-I ; Feng, Wu-Shiung ; Hsu, Chen-Yu

Electronics letters, 2014-01, Vol.50 (3), p.186-187 [Periódico revisado por pares]

Stevenage: The Institution of Engineering and Technology

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5
1 : 1 Adduct Ion Formation of Simple Carbohydrate Derivatives with Cations Using FAB Mass Spectrometry. Comparison of O-Acetyl, N-Butyl, and O-Methyl Modifications
1 : 1 Adduct Ion Formation of Simple Carbohydrate Derivatives with Cations Using FAB Mass Spectrometry. Comparison of O-Acetyl, N-Butyl, and O-Methyl Modifications
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1 : 1 Adduct Ion Formation of Simple Carbohydrate Derivatives with Cations Using FAB Mass Spectrometry. Comparison of O-Acetyl, N-Butyl, and O-Methyl Modifications

Sawada, Masami ; Shizuma, Motohiro ; Takai, Yoshio ; Yamada, Hitoshi ; Tanaka, Takanori ; Okumura, Yasuo ; Hidaka, Yukio ; Hanafusa, Terukiyo ; Takahashi, Shigetoshi

Bulletin of the Chemical Society of Japan, 1992-05, Vol.65 (5), p.1275-1279 [Periódico revisado por pares]

TOKYO: The Chemical Society of Japan

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6
1, 3-Dipolar Cycloaddition Reaction of 2-[(Trimethylsilylmethylamino)(methylthio)]methylene-1, 3-indandione and 2-[(Trimethylsilylmethylthio)(methylthio)]methylene-1, 3-indandione : Synthetic Equivalents of Cyclic Dicarbonyl Alkylideneazomethine and Alkylidenethiocarbonyl Ylides as Novel 1, 3-Dipolar Reagents
1, 3-Dipolar Cycloaddition Reaction of 2-[(Trimethylsilylmethylamino)(methylthio)]methylene-1, 3-indandione and 2-[(Trimethylsilylmethylthio)(methylthio)]methylene-1, 3-indandione : Synthetic Equivalents of Cyclic Dicarbonyl Alkylideneazomethine and Alkylidenethiocarbonyl Ylides as Novel 1, 3-Dipolar Reagents
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1, 3-Dipolar Cycloaddition Reaction of 2-[(Trimethylsilylmethylamino)(methylthio)]methylene-1, 3-indandione and 2-[(Trimethylsilylmethylthio)(methylthio)]methylene-1, 3-indandione : Synthetic Equivalents of Cyclic Dicarbonyl Alkylideneazomethine and Alkylidenethiocarbonyl Ylides as Novel 1, 3-Dipolar Reagents

TOMINAGA, Yoshinori ; TAKADA, Satoshi ; KOHRA, Shinya

Chemical and Pharmaceutical Bulletin, 1996/04/15, Vol.44(4), pp.653-660 [Periódico revisado por pares]

Tokyo: The Pharmaceutical Society of Japan

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7
1, 3-Dipolar Cycloaddition Reaction of Substituted Trimethylstannylacetylenes with Nitrile Oxides
1, 3-Dipolar Cycloaddition Reaction of Substituted Trimethylstannylacetylenes with Nitrile Oxides
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1, 3-Dipolar Cycloaddition Reaction of Substituted Trimethylstannylacetylenes with Nitrile Oxides

SAKAMOTO, Takao ; UCHIYAMA, Daishi ; KONDO, Yoshinori ; YAMANAKA, Hiroshi

Chemical and Pharmaceutical Bulletin, 1993/03/15, Vol.41(3), pp.478-480 [Periódico revisado por pares]

Tokyo: The Pharmaceutical Society of Japan

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8
1,1-Ethylboration of alkyn-1-yl-chloro(methyl)silanes: alkenes with chloro(methyl)silyl and diethylboryl groups in cis positions
1,1-Ethylboration of alkyn-1-yl-chloro(methyl)silanes: alkenes with chloro(methyl)silyl and diethylboryl groups in cis positions
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1,1-Ethylboration of alkyn-1-yl-chloro(methyl)silanes: alkenes with chloro(methyl)silyl and diethylboryl groups in cis positions

Wrackmeyer, Bernd ; Shahid, Khadija ; Ali, Saqib

Applied organometallic chemistry, 2005-03, Vol.19 (3), p.377-382 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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9
1,1-Organoboration of bis(trimethylstannyl)ethyne with trimethylsilyl- and dimethylsilyl-dialkylboryl-substituted alkenes: organometallic-substituted allenes
1,1-Organoboration of bis(trimethylstannyl)ethyne with trimethylsilyl- and dimethylsilyl-dialkylboryl-substituted alkenes: organometallic-substituted allenes
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1,1-Organoboration of bis(trimethylstannyl)ethyne with trimethylsilyl- and dimethylsilyl-dialkylboryl-substituted alkenes: organometallic-substituted allenes

Wrackmeyer, Bernd ; Tok, Oleg L. ; Bhatti, Moazzam H. ; Ali, Saqib

Applied organometallic chemistry, 2003-11, Vol.17 (11), p.843-850 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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10
1,2-Asymmetric induction in intramolecular Michael reaction. A novel and enantioselective route to (+)-Geissman lactone
1,2-Asymmetric induction in intramolecular Michael reaction. A novel and enantioselective route to (+)-Geissman lactone
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1,2-Asymmetric induction in intramolecular Michael reaction. A novel and enantioselective route to (+)-Geissman lactone

SHISHIDO, K ; SUKEGAWA, Y ; FUKUMOTO, K ; KAMETANI, T

Journal of the Chemical Society, Perkin Transactions 1, 1987 (5), p.993-1004 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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