Diastereoselective Synthesis of Bicyclo[2.2.2]octan-2-one Derivatives through an Unexpected Organocatalytic Tandem Michael-Michael Reaction

Synthesis ◽

10.1055/s-0030-1260052 ◽

2011 ◽

Vol 2011 (12) ◽

pp. 1984-1987 ◽

Author(s):

Jinxing Ye ◽

Juanjuan Yang ◽

Huicai Huang ◽

Zhichao Jin ◽

Wenbin Wu

Keyword(s):

Michael Reaction ◽

Diastereoselective Synthesis

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Diastereoselective synthesis of (−)-1-methyl-(3S,4R)-3,4-bis((2S)-N-(tert-butyloxycarbonyl)pyrrolidin-2-yl)-2-pyrrolidinone by an asymmetric Michael reaction

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(98)00241-9 ◽

1998 ◽

Vol 9 (13) ◽

pp. 2369-2376 ◽

Author(s):

Siavosh Mahboobi ◽

Alfred Popp ◽

Thomas Burgemeister ◽

Dieter Schollmeyer

Keyword(s):

Michael Reaction ◽

Diastereoselective Synthesis ◽

Asymmetric Michael Reaction

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Enantio- and Diastereoselective Synthesis of Piperidines by Coupling of Four Components in a “One-Pot” Sequence Involving Diphenylprolinol Silyl Ether Mediated Michael Reaction

Organic Letters ◽

10.1021/ol1018932 ◽

2010 ◽

Vol 12 (20) ◽

pp. 4588-4591 ◽

Author(s):

Tatsuya Urushima ◽

Daisuke Sakamoto ◽

Hayato Ishikawa ◽

Yujiro Hayashi

Keyword(s):

Michael Reaction ◽

Silyl Ether ◽

Diastereoselective Synthesis ◽

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The Diastereoselective Synthesis of Ester-Functionalized Alkenes through the Stereocontrolled Conjugate Addition (Michael Reaction) of Prochiral Enolates to Chiral .alpha.-Methylene .beta.-Lactones and Thermal Decarboxylation of the Resulting .alpha.-Substituted .beta.-Lactones

The Journal of Organic Chemistry ◽

10.1021/jo00117a045 ◽

1995 ◽

Vol 60 (12) ◽

pp. 3879-3886 ◽

Author(s):

Victor Oswaldo Nava-Salgado ◽

Eva-Maria Peters ◽

Karl Peters ◽

Hans Georg von Schnering ◽

Waldemar Adam

Keyword(s):

Michael Reaction ◽

Conjugate Addition ◽

Diastereoselective Synthesis ◽

Thermal Decarboxylation

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Tandem imino-pinacol coupling-aza-Michael reaction promoted by Zn/InCl3: a novel multicomponent strategy for diastereoselective synthesis of monocyclic 1,4-diazepine in water

New Journal of Chemistry ◽

10.1039/c2nj40469a ◽

2012 ◽

Vol 36 (11) ◽

pp. 2209 ◽

Author(s):

I. R. Siddiqui ◽

Shayna Shamim ◽

Devesh Kumar ◽

Shireen ◽

Malik A. Waseem

Keyword(s):

Michael Reaction ◽

Diastereoselective Synthesis ◽

Pinacol Coupling

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Iodotrimethylsilane Induced Diastereoselective Synthesis of Tetrahydropyranones by a Tandem Knoevenagel—Michael Reaction.

10.1002/chin.200352138 ◽

2003 ◽

Vol 34 (52) ◽

Author(s):

Gowravaram Sabitha ◽

G. S. Kiran Kumar Reddy ◽

M. Rajkumar ◽

J. S. Yadav ◽

K. V. S. Ramakrishna ◽

...

Keyword(s):

Michael Reaction ◽

Diastereoselective Synthesis

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Intramolecular Michael Reaction in Diastereoselective Synthesis of dl-Griseofulvin.

Chemical and Pharmaceutical Bulletin ◽

10.1248/cpb.39.3048 ◽

1991 ◽

Vol 39 (11) ◽

pp. 3048-3050 ◽

Author(s):

Yasuo TAKEUCHI ◽

Ikuo WATANABE ◽

Hideo TOMOZANE ◽

Kuniko HASHIGAKI ◽

Masatoshi YAMATO

Keyword(s):

Michael Reaction ◽

Diastereoselective Synthesis

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ChemInform Abstract: Michael Reaction of Nitroalkanes with β-Nitroacrylates under a Solid Promoter: Advanced Regio- and Diastereoselective Synthesis of Nitro-Functionalized α,β-Unsaturated Esters and 1,3-Butadiene-2-carboxylates.

10.1002/chin.201045041 ◽

2010 ◽

Vol 41 (45) ◽

pp. no-no

Author(s):

Alessandro Palmieri ◽

Serena Gabrielli ◽

Roberto Ballini

Keyword(s):

Michael Reaction ◽

Diastereoselective Synthesis ◽

Unsaturated Esters

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Diastereoselective Synthesis of Multisubstituted Chroman Derivatives via Iminium Formation/Morita-Baylis-Hillman Reaction/Oxa-Michael Reaction Sequence

Chemistry Letters ◽

10.1246/cl.180988 ◽

2019 ◽

Vol 48 (4) ◽

pp. 337-340

Author(s):

Natsuki Ido ◽

Keiji Mori

Keyword(s):

Michael Reaction ◽

Diastereoselective Synthesis ◽

Reaction Sequence

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The Oxidative Michael Reaction. A Highly Diastereoselective Synthesis of 5-Oxocarboxylic Acid Derivatives

Chemistry Letters ◽

10.1246/cl.1986.1623 ◽

1986 ◽

Vol 15 (9) ◽

pp. 1623-1626 ◽

Author(s):

Yukihiko Hashimoto ◽

Teruaki Mukaiyama

Keyword(s):

Michael Reaction ◽

Diastereoselective Synthesis

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Diastereoselective synthesis of trifluoromethylated 1,3-dioxanes by intramolecular oxa-Michael reaction

Organic & Biomolecular Chemistry ◽

10.1039/c6ob02333a ◽

2017 ◽

Vol 15 (2) ◽

pp. 301-305 ◽

Author(s):

Liliana Becerra-Figueroa ◽

Elodie Brun ◽

Michael Mathieson ◽

Louis J. Farrugia ◽

Claire Wilson ◽

...

Keyword(s):

Michael Reaction ◽

Diastereoselective Synthesis ◽

Simple Method ◽

Reaction Proceeds

A rapid and simple method to access trifluoromethylated 1,3-dioxanes by a sequence of addition/oxa-Michael reaction has been developed; the reaction proceeds smoothly with excellent stereoselectivity.

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