Catalytic Asymmetric 1,3-Dipolar Cycloaddition of α,β-Unsaturated Amide and Azomethine Imine

α,β-Unsaturated Amides as Dipolarophiles: Catalytic Asymmetric exo -Selective 1,3-Dipolar Cycloaddition with Nitrones

10.1002/chem.201703250 ◽

2017 ◽

Vol 23 (51) ◽

pp. 12424-12424 ◽

Cited By ~ 1

Author(s):

Ming Zhang ◽

Naoya Kumagai ◽

Masakatsu Shibasaki

Keyword(s):

Dipolar Cycloaddition ◽

ChemInform Abstract: Catalytic Asymmetric 1,3-Dipolar Cycloaddition of α-Iminonitriles.

ChemInform ◽

10.1002/chin.201038116 ◽

2010 ◽

Vol 41 (38) ◽

pp. no-no

Author(s):

Rocio Robles-Machin ◽

Ines Alonso ◽

Javier Adrio ◽

Juan C. Carretero

Keyword(s):

Dipolar Cycloaddition ◽

Microwave-assisted facile synthesis of [a]-annelated pyrazolopyrroloindoles via intramolecular azomethine imine 1,3-dipolar cycloaddition

Tetrahedron Letters ◽

10.1016/j.tetlet.2014.03.134 ◽

2014 ◽

Vol 55 (19) ◽

pp. 3064-3069 ◽

Cited By ~ 25

Author(s):

Anand H. Shinde ◽

Shinde Vidyacharan ◽

Duddu S. Sharada

Keyword(s):

Dipolar Cycloaddition ◽

Facile Synthesis ◽

Azomethine Imine ◽

Microwave Assisted

α,β‐Unsaturated Amides as Dipolarophiles: Catalytic Asymmetric exo ‐Selective 1,3‐Dipolar Cycloaddition with Nitrones

10.1002/chem.201702330 ◽

2017 ◽

Vol 23 (51) ◽

pp. 12450-12455 ◽

Cited By ~ 8

Author(s):

Ming Zhang ◽

Naoya Kumagai ◽

Masakatsu Shibasaki

Keyword(s):

Dipolar Cycloaddition ◽

Synthesis of Highly Functionalized Tricyclic Chromenopyrazole Frameworks via Intramolecular Azomethine Imine 1,3-Dipolar Cycloaddition (IAIDC)

ChemistrySelect ◽

10.1002/slct.201801269 ◽

2018 ◽

Vol 3 (24) ◽

pp. 6960-6964 ◽

Cited By ~ 9

Author(s):

Manickam Bakthadoss ◽

Vishal Agarwal

Keyword(s):

Dipolar Cycloaddition ◽

Azomethine Imine

Catalytic Asymmetric 1,3-Dipolar Cycloaddition of α-Iminonitriles

10.1002/chem.200903443 ◽

2010 ◽

Vol 16 (18) ◽

pp. 5286-5291 ◽

Cited By ~ 44

Author(s):

Rocío Robles-Machín ◽

Inés Alonso ◽

Javier Adrio ◽

Juan C. Carretero

Keyword(s):

Dipolar Cycloaddition ◽

The catalytic asymmetric synthesis of CF3-containing spiro-oxindole–pyrrolidine–pyrazolone compounds through squaramide-catalyzed 1,3-dipolar cycloaddition

Organic & Biomolecular Chemistry ◽

10.1039/c9ob00720b ◽

2019 ◽

Vol 17 (22) ◽

pp. 5514-5519 ◽

Cited By ~ 12

Author(s):

Cui Wang ◽

Dongwa Wen ◽

Hui Chen ◽

Yabo Deng ◽

Xueting Liu ◽

...

Keyword(s):

Asymmetric Synthesis ◽

Cycloaddition Reaction ◽

Dipolar Cycloaddition ◽

Catalytic Asymmetric Synthesis ◽

Pharmaceutically important compounds were synthesized through the organocatalytic 1,3-dipolar cycloaddition reaction.

Front Picture: α,β-Unsaturated Amides as Dipolarophiles: Catalytic Asymmetric exo -Selective 1,3-Dipolar Cycloaddition with Nitrones (Chem. Eur. J. 51/2017)

10.1002/chem.201703251 ◽

2017 ◽

Vol 23 (51) ◽

pp. 12420-12420

Author(s):

Ming Zhang ◽

Naoya Kumagai ◽

Masakatsu Shibasaki

Keyword(s):

Dipolar Cycloaddition ◽

Catalytic Asymmetric ◽

J 51

Crystal Structure of a Chiral Titanium Catalyst-Alkene Complex. The Intermediate in Catalytic Asymmetric Diels-Alder and 1,3-Dipolar Cycloaddition Reactions

Journal of the American Chemical Society ◽

10.1021/ja00120a041 ◽

1995 ◽

Vol 117 (15) ◽

pp. 4435-4436 ◽

Cited By ~ 65

Author(s):

Kurt V. Gothelf ◽

Rita G. Hazell ◽

Karl Anker Jorgensen

Keyword(s):

Crystal Structure ◽

Diels Alder ◽

Dipolar Cycloaddition ◽

Cycloaddition Reactions ◽

Titanium Catalyst ◽

Catalytic Asymmetric 1,3-Dipolar Cycloaddition Reactions Based on Ylide Formation Reactions

Journal of Synthetic Organic Chemistry Japan ◽

10.5059/yukigoseikyokaishi.77.1014 ◽

2019 ◽

Vol 77 (10) ◽

pp. 1014-1022

Author(s):

Hiroyuki Suga ◽

Yasunori Toda

Keyword(s):

Dipolar Cycloaddition ◽

Cycloaddition Reactions ◽