Eur. J. Inorg. Chem.
 1999
DOI: 10.1002/(sici)1099-0682(199901)1999:1<153::aid-ejic153>3.3.co;2-s
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John J. Eisch
1
,
Katrin Mackenzie
2
,
Harald Windisch
3
et al.
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Cited by 23 publications

(39 citation statements)
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“…In this case, iodoboration occurred rapidly and compound 18 was obtained ( Scheme 5a ). 17 Siebert found that iodoboration of 3-hexyne with BI 3 furnished the syn -addition product 19 rapidly, which, in line with Wrackmeyer's observations, underwent slow isomerisation to form the anti -addition product 20 at room temperature ( Scheme 5b ). 18,19 …”
Section: Haloboration Of Simple Alkynes Using Y 2 B–x (Y = X or R)supporting
confidence: 55%
Exaggerated anticipatory anxiety is common in social anxiety disorder (SAD). Neuroimaging studies have revealed altered neural activity in response to social stimuli in SAD, but fewer studies have examined neural activity during anticipation of feared social stimuli in SAD. The current study examined the time course and magnitude of activity in threat processing brain regions during speech anticipation in socially anxious individuals and healthy controls (HC). Method Participants (SAD n = 58; HC n = 16) underwent functional magnetic resonance imaging (fMRI) during which they completed a 90s control anticipation task and 90s speech anticipation task.
“…In this case, iodoboration occurred rapidly and compound 18 was obtained ( Scheme 5a ). 17 Siebert found that iodoboration of 3-hexyne with BI 3 furnished the syn -addition product 19 rapidly, which, in line with Wrackmeyer's observations, underwent slow isomerisation to form the anti -addition product 20 at room temperature ( Scheme 5b ). 18,19 …”
Section: Haloboration Of Simple Alkynes Using Y 2 B–x (Y = X or R)supporting
confidence: 55%
Exaggerated anticipatory anxiety is common in social anxiety disorder (SAD). Neuroimaging studies have revealed altered neural activity in response to social stimuli in SAD, but fewer studies have examined neural activity during anticipation of feared social stimuli in SAD. The current study examined the time course and magnitude of activity in threat processing brain regions during speech anticipation in socially anxious individuals and healthy controls (HC). Method Participants (SAD n = 58; HC n = 16) underwent functional magnetic resonance imaging (fMRI) during which they completed a 90s control anticipation task and 90s speech anticipation task.
“…Thus n BuSnCl 3 modifies silica as well as MAO. The work of Eisch and co‐workers indirectly supports this postulation (Scheme (b)). Consequently, the overall Lewis acid strength of Catalyst 2 partially decreases.…”
Section: Resultsmentioning
confidence: 72%
“…The lower polymerization activity of Catalyst 2 incidentally supports this remark. The literature reports that the MAO Lewis acid site originates from the coordinatively unsaturated Al in an –AlO 2 Me– environment (which consists of the tri‐coordinated Al atoms bridging the tri‐coordinated oxygen atoms) …”
Section: Resultsmentioning
confidence: 99%
Exaggerated anticipatory anxiety is common in social anxiety disorder (SAD). Neuroimaging studies have revealed altered neural activity in response to social stimuli in SAD, but fewer studies have examined neural activity during anticipation of feared social stimuli in SAD. The current study examined the time course and magnitude of activity in threat processing brain regions during speech anticipation in socially anxious individuals and healthy controls (HC). Method Participants (SAD n = 58; HC n = 16) underwent functional magnetic resonance imaging (fMRI) during which they completed a 90s control anticipation task and 90s speech anticipation task.
“…One is the early study of the diphenylacetylene/PhBBr 2 /K system by Lappert et al,13 in which they claimed to have obtained a perphenylated 1,4‐diboracyclohexadiene derivative or an unknown carborane species. These results, however, could not be reproduced by Eisch et al14 The other system involves the alkynes/MeBBr 2 /C 8 K reaction reported by van der Kerk et al,15 who claimed to have obtained stable peralkylated 1,4‐diboracyclohexadiene derivatives as the main products through a borylene mechanism, while Wrackmeyer et al16 (in the cases of 3‐hexyne and 5‐decyne) obtained the corresponding C 4 B 2 ‐ nido ‐carboranes. No 1,4‐diboracyclohexadiene derivatives could be detected.…”
Section: Resultsmentioning
confidence: 92%
Exaggerated anticipatory anxiety is common in social anxiety disorder (SAD). Neuroimaging studies have revealed altered neural activity in response to social stimuli in SAD, but fewer studies have examined neural activity during anticipation of feared social stimuli in SAD. The current study examined the time course and magnitude of activity in threat processing brain regions during speech anticipation in socially anxious individuals and healthy controls (HC). Method Participants (SAD n = 58; HC n = 16) underwent functional magnetic resonance imaging (fMRI) during which they completed a 90s control anticipation task and 90s speech anticipation task.
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