ChemInform Abstract: Lewis Acid-Catalyzed Reactions of N-Allylanilines with Diazo Compounds Involving Aza-Claisen Rearrangement.

10.1002/chin.201619066 ◽

2016 ◽

Vol 47 (19) ◽

Author(s):

Alexander G. Badamshin ◽

Leonid V. Spirikhin ◽

Rinat F. Salikov ◽

Vladimir A. Dokichev ◽

Yury V. Tomilov

Keyword(s):

Claisen Rearrangement ◽

Diazo Compounds ◽

Acid Catalyzed ◽

Catalyzed Reactions

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Lewis acid-catalyzed reactions of N-allylanilines with diazo compounds involving aza-Claisen rearrangement

Mendeleev Communications ◽

10.1016/j.mencom.2015.11.013 ◽

2015 ◽

Vol 25 (6) ◽

pp. 438-439 ◽

Author(s):

Alexander G. Badamshin ◽

Leonid V. Spirikhin ◽

Rinat F. Salikov ◽

Vladimir A. Dokichev ◽

Yury V. Tomilov

Keyword(s):

Claisen Rearrangement ◽

Diazo Compounds ◽

Acid Catalyzed ◽

Catalyzed Reactions

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Synthesis of Novel Silicon-Containing Compounds via Lewis Acid Catalyzed Reactions

10.1002/chin.200617263 ◽

2006 ◽

Vol 37 (17) ◽

Author(s):

Il Nam Jung ◽

Bok Ryul Yoo

Keyword(s):

Acid Catalyzed ◽

Catalyzed Reactions

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Lewis Acid Catalyzed Site-Selective Cycloadditions of 2,6-Diazasemibullvalenes with Isocyanides, Azides, and Diazo Compounds for the Synthesis of Diaza- and Triazabrexadiene Derivatives

Angewandte Chemie International Edition ◽

10.1002/anie.201210126 ◽

2013 ◽

Vol 52 (12) ◽

pp. 3485-3489 ◽

Author(s):

Shaoguang Zhang ◽

Wen-Xiong Zhang ◽

Zhenfeng Xi

Keyword(s):

Diazo Compounds ◽

Acid Catalyzed ◽

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ChemInform Abstract: The Preparation of Optically Active δ2-Isoxazolines. A Model for Asymmetric Induction in the Non Lewis Acid Catalyzed Reactions of Oppolzer′s Chiral Sultam.

10.1002/chin.198852160 ◽

1988 ◽

Vol 19 (52) ◽

Author(s):

D. P. CURRAN ◽

B. H. KIM ◽

J. DAUGHERTY ◽

T. A. HEFFNER

Keyword(s):

Optically Active ◽

Asymmetric Induction ◽

Acid Catalyzed ◽

Catalyzed Reactions

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Lewis acid-catalyzed reactions of mono-aryl group substituted methylenecyclopropanes with diethyl ketomalonate

Tetrahedron ◽

10.1016/j.tet.2007.03.040 ◽

2007 ◽

Vol 63 (21) ◽

pp. 4535-4542 ◽

Author(s):

Le-Ping Liu ◽

Min Shi

Keyword(s):

Acid Catalyzed ◽

Catalyzed Reactions

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ChemInform Abstract: Lewis Acid Catalyzed Reactions in Aqueous Solution.

10.1002/chin.199546061 ◽

2010 ◽

Vol 26 (46) ◽

pp. no-no

Author(s):

S. KOBAYASHI ◽

I. HACHIYA

Keyword(s):

Aqueous Solution ◽

Acid Catalyzed ◽

Catalyzed Reactions

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Combination of enzyme- and Lewis acid-catalyzed reactions: a new method for the synthesis of 6,7-dihydrobenzofuran-4(5H)-ones starting from 2,5-dimethylfuran and 1,3-cyclohexanediones

Organic & Biomolecular Chemistry ◽

10.1039/c3ob40926k ◽

2013 ◽

Vol 11 (34) ◽

pp. 5692 ◽

Author(s):

Chimène Asta ◽

Dietmar Schmidt ◽

Jürgen Conrad ◽

Wolfgang Frey ◽

Uwe Beifuss

Keyword(s):

Acid Catalyzed ◽

Catalyzed Reactions

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ChemInform Abstract: Synthesis of Pyrrolo[1,2-a]quinoxaline and Its 4-(1-Hydroxyalkyl) Derivatives by Lewis Acid-Catalyzed Reactions of 1-(2-Isocyanophenyl)pyrrole.

10.1002/chin.199844157 ◽

2010 ◽

Vol 29 (44) ◽

pp. no-no

Author(s):

K. KOBAYASHI ◽

S. MATOBA ◽

S. IRISAWA ◽

T. MATSUMOTO ◽

O. MORIKAWA ◽

...

Keyword(s):

Acid Catalyzed ◽

Catalyzed Reactions

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Lewis acid catalyzed reactions of donor–acceptor cyclopropanes with 1- and 2-pyrazolines: formation of substituted 2-pyrazolines and 1,2-diazabicyclo[3.3.0]octanes

Tetrahedron ◽

10.1016/j.tet.2010.09.092 ◽

2010 ◽

Vol 66 (47) ◽

pp. 9151-9158 ◽

Author(s):

Yury V. Tomilov ◽

Roman A. Novikov ◽

Oleg M. Nefedov

Keyword(s):

Donor Acceptor ◽

Acid Catalyzed ◽

Catalyzed Reactions

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Structural reconstruction: a milestone in the hydrothermal synthesis of highly active Sn-Beta zeolites

Chemical Communications ◽

10.1039/c7cc06778j ◽

2017 ◽

Vol 53 (93) ◽

pp. 12516-12519 ◽

Author(s):

Zhiguo Zhu ◽

Hao Xu ◽

Jingang Jiang ◽

Haihong Wu ◽

Peng Wu

Keyword(s):

Hydrothermal Synthesis ◽

State Of The Art ◽

Highly Active ◽

Beta Zeolites ◽

Acid Catalyzed ◽

Catalyzed Reactions ◽

Catalytic Performances

Hydrophobic Sn-Beta zeolites, hydrothermally synthesized via structural reconstruction, exhibit unparalleled catalytic performances for Lewis acid-catalyzed reactions, far outperforming post-synthesized Sn-Beta and state-of-the-art Sn-Beta-F materials.

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