Synthesis of O-tert-Butyl-N,N-disubstituted Hydroxylamines by N–O Bond Formation

ChemInform Abstract: Facile Amide Bond Formation from Esters of Amino Acids and Peptides, e. g. (S)-(I), Catalyzed by Alkaline Protease in Anhydrous tert-Butyl Alcohol Using Ammonium Chloride/Triethylamine as a Source of Nucleophilic Ammonia.

ChemInform ◽

10.1002/chin.199406221 ◽

2010 ◽

Vol 25 (6) ◽

pp. no-no

Author(s):

S.-T. CHEN ◽

M.-K. JANG ◽

K.-T. WANG

Keyword(s):

Amino Acids ◽

Ammonium Chloride ◽

Alkaline Protease ◽

Bond Formation ◽

Butyl Alcohol ◽

Amide Bond ◽

Tert Butyl ◽

Amide Bond Formation ◽

Tert Butyl Alcohol

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ChemInform Abstract: Novel CâS Bond Formation Through Î±â²,Î²-Elimination of tert-Butyl Sulfoxonium Ylides: A Facile Approach to Chiral Sulfoxides.

ChemInform ◽

10.1002/chin.200952099 ◽

2009 ◽

Vol 40 (52) ◽

Author(s):

Xiao-Yu Guan ◽

Zhang-Qin Liu ◽

Hao-Xi Huang ◽

Li-Ping Yang ◽

Liao Jian ◽

...

Keyword(s):

Bond Formation ◽

Tert Butyl ◽

Chiral Sulfoxides

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Selective C O bond formation: highly efficient radical dioxygenation of alkenes initiated by catalytic amount of tert-butyl hydroperoxide

Tetrahedron ◽

10.1016/j.tet.2016.10.029 ◽

2016 ◽

Vol 72 (49) ◽

pp. 8000-8003 ◽

Cited By ~ 9

Author(s):

Xiao-Feng Xia ◽

Su-Li Zhu ◽

Qing-Tao Hu ◽

Chao Chen

Keyword(s):

Bond Formation ◽

Catalytic Amount ◽

Butyl Hydroperoxide ◽

Tert Butyl ◽

Highly Efficient ◽

Tert Butyl Hydroperoxide

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Difference in Photochemical Behavior in 3,6- and 2,5-Di-tert-butyl-3H-azepine: The First Photochemical Bond Formation Between 2- and 6-Position of 3H-Azepine Ring.

ChemInform ◽

10.1002/chin.200317046 ◽

2003 ◽

Vol 34 (17) ◽

Author(s):

Kyosuke Satake ◽

Shizuka Takami ◽

Yuko Tawada ◽

Masaru Kimura

Keyword(s):

Bond Formation ◽

Photochemical Behavior ◽

Tert Butyl

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Difference in photochemical behavior in 3,6- and 2,5-di-tert-butyl-3H-azepine: The first photochemical bond formation between 2- and 6-position of 3H-azepine ring

Journal of Heterocyclic Chemistry ◽

10.1002/jhet.5570390637 ◽

2002 ◽

Vol 39 (6) ◽

pp. 1337-1338 ◽

Cited By ~ 2

Author(s):

Kyosuke Satake ◽

Yuko Tawada ◽

Shizuka Takami ◽

Masaru Kimura

Keyword(s):

Bond Formation ◽

Photochemical Behavior ◽

Tert Butyl

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REACTION OF SEVEN- AND EIGHT-MEMBERED CYCLIC PHOSPHOROCHLORIDITES WITH 3,5-DI-tert-BUTYL-4-HYDROXYBENZYL ALCOHOL: FACILE P[sbnd]C BOND FORMATION

Phosphorous and Sulfur and the Related Elements ◽

10.1080/03086648408077637 ◽

1984 ◽

Vol 20 (3) ◽

pp. 273-277 ◽

Cited By ~ 9

Author(s):

Paul A. Odorisio ◽

Stephen D. Pastor ◽

John D. Spivack

Keyword(s):

Bond Formation ◽

Tert Butyl ◽

Hydroxybenzyl Alcohol

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Copper-Catalyzed Oxidative Dimerization of 2-Oxindoles under Base-Free Conditions

Synlett ◽

10.1055/s-0037-1609757 ◽

2018 ◽

Vol 29 (11) ◽

pp. 1485-1490 ◽

Cited By ~ 2

Author(s):

Wen-Ting Wei ◽

Yi-Ling Huang ◽

Wen-Hui Bao ◽

Wei-Wei Ying ◽

Wei-Ting Chen ◽

...

Keyword(s):

Bond Formation ◽

Radical Mechanism ◽

Oxidative Dimerization ◽

Radical Initiator ◽

Tert Butyl ◽

Simple Strategy ◽

Efficient Route ◽

Butyl Peroxide

A practical copper-catalyzed oxidative dimerization of 2-oxindoles using di-tert-butyl peroxide as the radical initiator under base-free conditions was achieved, which not only provided an efficient route to prepare various 3,3′-bioxindoles, but also represented a simple strategy for C(sp3)–H functionalization/C–C bond formation. A radical mechanism was proposed based on the reaction results and controlling experiments.

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ChemInform Abstract: REACTION OF SEVEN- AND EIGHT-MEMBERED CYCLIC PHOSPHOROCHLORIDITES WITH 3,5-DI-TERT-BUTYL-4-HYDROXYBENZYL ALCOHOL: FACILE PHOSPHORUS-CARBON BOND FORMATION

Chemischer Informationsdienst ◽

10.1002/chin.198543296 ◽

1985 ◽

Vol 16 (43) ◽

Author(s):

P. A. ODORISIO ◽

S. D. PASTOR ◽

J. D. SPIVACK

Keyword(s):

Bond Formation ◽

Carbon Bond ◽

Tert Butyl ◽

Hydroxybenzyl Alcohol

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Novel C-S Bond Formation Through α’,β-Elimination of tert-Butyl Sulfoxonium Ylides: A Facile Approach to Chiral Sulfoxides

Synlett ◽

10.1055/s-0029-1217572 ◽

2009 ◽

Vol 2009 (13) ◽

pp. 2183-2187 ◽

Cited By ~ 1

Author(s):

Liao Jian ◽

Wen-Hao Hu ◽

Xiao-Yu Guan ◽

Zhang-Qin Liu ◽

Hao-Xi Huang ◽

...

Keyword(s):

Bond Formation ◽

Tert Butyl ◽

Chiral Sulfoxides

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Reversible Bond Formation and Cleavage of the Oxo Bridge of [Ru2(μ-O)(dioxolene)2(btpyxa)]3+ [btpyxa = 2,7-Di-tert-butyl-9,9-dimethyl-4,5-bis(2,2′:6′,2′′-terpyrid-4′-yl)xanthene] Driven by a Three-Electron Redox Reaction

European Journal of Inorganic Chemistry ◽

10.1002/ejic.200500141 ◽

2005 ◽

Vol 2005 (19) ◽

pp. 3832-3839 ◽

Cited By ~ 13

Author(s):

Tohru Wada ◽

Koji Tanaka

Keyword(s):

Redox Reaction ◽

Bond Formation ◽

Tert Butyl ◽

Oxo Bridge

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Synthesis of O-tert-Butyl-N,N-disubstituted Hydroxylamines by N–O Bond Formation

ChemInform Abstract: Facile Amide Bond Formation from Esters of Amino Acids and Peptides, e. g. (S)-(I), Catalyzed by Alkaline Protease in Anhydrous tert-Butyl Alcohol Using Ammonium Chloride/Triethylamine as a Source of Nucleophilic Ammonia.

ChemInform Abstract: Novel CâS Bond Formation Through Î±â²,Î²-Elimination of tert-Butyl Sulfoxonium Ylides: A Facile Approach to Chiral Sulfoxides.

Selective C O bond formation: highly efficient radical dioxygenation of alkenes initiated by catalytic amount of tert-butyl hydroperoxide

Difference in Photochemical Behavior in 3,6- and 2,5-Di-tert-butyl-3H-azepine: The First Photochemical Bond Formation Between 2- and 6-Position of 3H-Azepine Ring.

Difference in photochemical behavior in 3,6- and 2,5-di-tert-butyl-3H-azepine: The first photochemical bond formation between 2- and 6-position of 3H-azepine ring

REACTION OF SEVEN- AND EIGHT-MEMBERED CYCLIC PHOSPHOROCHLORIDITES WITH 3,5-DI-tert-BUTYL-4-HYDROXYBENZYL ALCOHOL: FACILE P[sbnd]C BOND FORMATION

Copper-Catalyzed Oxidative Dimerization of 2-Oxindoles under Base-Free Conditions

ChemInform Abstract: REACTION OF SEVEN- AND EIGHT-MEMBERED CYCLIC PHOSPHOROCHLORIDITES WITH 3,5-DI-TERT-BUTYL-4-HYDROXYBENZYL ALCOHOL: FACILE PHOSPHORUS-CARBON BOND FORMATION

Novel C-S Bond Formation Through α’,β-Elimination of tert-Butyl Sulfoxonium Ylides: A Facile Approach to Chiral Sulfoxides

Reversible Bond Formation and Cleavage of the Oxo Bridge of [Ru2(μ-O)(dioxolene)2(btpyxa)]3+ [btpyxa = 2,7-Di-tert-butyl-9,9-dimethyl-4,5-bis(2,2′:6′,2′′-terpyrid-4′-yl)xanthene] Driven by a Three-Electron Redox Reaction

ChemInform Abstract: Novel CâS Bond Formation Through Î±â²,Î²-Elimination of tert-Butyl Sulfoxonium Ylides: A Facile Approach to Chiral Sulfoxides.