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1,1-Dibromo-1-alkenes as Valuable Partners in the Copper-Catalyzed Direct Alkynylation of Azoles
1,1-Dibromo-1-alkenes as Valuable Partners in the Copper-Catalyzed Direct Alkynylation of Azoles
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1,1-Dibromo-1-alkenes as Valuable Partners in the Copper-Catalyzed Direct Alkynylation of Azoles

Pacheco Berciano, Beatriz ; Lebrequier, Sabrina ; Besselièvre, François ; Piguel, Sandrine

Organic letters, 2010-09-17, Vol.12 (18), p.4038-4041 [Peer Reviewed Journal]

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2
1,1-EMborierung von 1-Trimethylsilylalkinen/ 1.1-Diboration of 1-Trimethylsilylalkines
1,1-EMborierung von 1-Trimethylsilylalkinen/ 1.1-Diboration of 1-Trimethylsilylalkines
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1,1-EMborierung von 1-Trimethylsilylalkinen/ 1.1-Diboration of 1-Trimethylsilylalkines

Klusik, Hartmut ; Pues, Christine ; Berndt, Armin

Zeitschrift für Naturforschung. B, A journal of chemical sciences, 1984-08-01, Vol.39 (8), p.1042-1045

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3
1,1-Ethylboration of Alkyn-1-yl- (dichloro)silanes: Alkenes Bearing Dichlorosilyl and Diethylboryl Groups
1,1-Ethylboration of Alkyn-1-yl- (dichloro)silanes: Alkenes Bearing Dichlorosilyl and Diethylboryl Groups
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1,1-Ethylboration of Alkyn-1-yl- (dichloro)silanes: Alkenes Bearing Dichlorosilyl and Diethylboryl Groups

Wrackmeyer, Bernd ; Shahid, Khadija ; Ali, Saqib

Zeitschrift für Naturforschung. B, A journal of chemical sciences, 2005-05-01, Vol.60 (5), p.590-592

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4
1,1-Ethylboration of ethynyl(trimethyl)tin. (E)-1-Trimethylstannyl-2-diethylboryl-but-1-ene, isomerization and conversion into hydridoborates
1,1-Ethylboration of ethynyl(trimethyl)tin. (E)-1-Trimethylstannyl-2-diethylboryl-but-1-ene, isomerization and conversion into hydridoborates
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1,1-Ethylboration of ethynyl(trimethyl)tin. (E)-1-Trimethylstannyl-2-diethylboryl-but-1-ene, isomerization and conversion into hydridoborates

Bernd Wrackmeyer ; Oleg L. Tok ; Peter Thoma

ARKIVOC free online journal of organic chemistry, 2007-04-30, Vol.2008 (5), p.6-18 [Peer Reviewed Journal]

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5
1.10 Multiply Bonded Compounds of Group 13 Elements
1.10 Multiply Bonded Compounds of Group 13 Elements
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1.10 Multiply Bonded Compounds of Group 13 Elements

Fischer, RC

Comprehensive Inorganic Chemistry II : From Elements to Applications, 2013, Vol.1, p.269-287

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1.11 Multiply Bonded Compounds of Group 14 Elements
1.11 Multiply Bonded Compounds of Group 14 Elements
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1.11 Multiply Bonded Compounds of Group 14 Elements

Sekiguchi, A ; Lee, V

Comprehensive Inorganic Chemistry II : From Elements to Applications, 2013, Vol.1, p.289-324

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1.15 Olefination of Carbonyl Compounds by Main-Group Element Mediators
1.15 Olefination of Carbonyl Compounds by Main-Group Element Mediators
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1.15 Olefination of Carbonyl Compounds by Main-Group Element Mediators

Blakemore, P.R

Comprehensive Organic Synthesis, 2014, p.516-608

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1.18 Low-Coordinate Main Group Compounds – Group 14 (Si, Ge)
1.18 Low-Coordinate Main Group Compounds – Group 14 (Si, Ge)
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1.18 Low-Coordinate Main Group Compounds – Group 14 (Si, Ge)

Tokitoh, N ; Sasamori, T

Comprehensive Inorganic Chemistry II : From Elements to Applications, 2013, Vol.1, p.567-577

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1,2-Addition of α,α,α-Trichlorotoluene to Ketones via a Mg Barbier Reaction in DMF: New Route to Cycloalk-1-en-1-yl and Alk-1-en-1-yl Phenyl Ketones
1,2-Addition of α,α,α-Trichlorotoluene to Ketones via a Mg Barbier Reaction in DMF: New Route to Cycloalk-1-en-1-yl and Alk-1-en-1-yl Phenyl Ketones
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1,2-Addition of α,α,α-Trichlorotoluene to Ketones via a Mg Barbier Reaction in DMF: New Route to Cycloalk-1-en-1-yl and Alk-1-en-1-yl Phenyl Ketones

Aaziz, Akima ; Oudeyer, Sylvain ; Léonel, Eric ; Paugam, Jean Paul ; Nédélec, Jean-Yves

Synthetic communications, 2007-04-01, Vol.37 (7), p.1147-1154 [Peer Reviewed Journal]

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10
1,2‐(Bis)trifluoromethylation of Alkynes: A One‐Step Reaction to Install an Underutilized Functional Group
1,2‐(Bis)trifluoromethylation of Alkynes: A One‐Step Reaction to Install an Underutilized Functional Group
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1,2‐(Bis)trifluoromethylation of Alkynes: A One‐Step Reaction to Install an Underutilized Functional Group

Guo, Shuo ; AbuSalim, Deyaa I ; Cook, Silas P

Angewandte Chemie, 2019-08-19, Vol.131 (34), p.11830-11834 [Peer Reviewed Journal]

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