Highly stereocontrolled sequential asymmetric Michael addition reactions with cinnamate esters - generation of three and four contiguous stereogenic centers on seven-carbon acyclic motifs

Stereogenic Centers

ChemInform Abstract: Highly Stereocontrolled Sequential Asymmetric Michael Addition Reactions with Cinnamate Esters - Generation of Three and Four Contiguous Stereogenic Centers on Seven-Carbon Acyclic Motifs.

ChemInform ◽

10.1002/chin.199511067 ◽

2010 ◽

Vol 26 (11) ◽

pp. no-no

Author(s):

S. HANESSIAN ◽

A. GOMTSYAN

Keyword(s):

Michael Addition ◽

Addition Reactions ◽

Stereogenic Centers

The carbamate esters as organocatalysts in asymmetric Michael addition reactions in aqueous media: when pyrrolidine backbone surpasses 1,2-diaminocyclohexane

ARKIVOC ◽

10.24820/ark.5550190.p010.692 ◽

2018 ◽

Vol 2018 (7) ◽

pp. 320-331 ◽

Cited By ~ 3

Author(s):

Anirban Mondal ◽

Kartick C. Bhowmick

Keyword(s):

Michael Addition ◽

Aqueous Media ◽

Addition Reactions ◽

Asymmetric Michael Addition Reactions with Chiral αβ-Unsaturated N-Acyloxazolidinones

19th International Congress on Heterocyclic Chemistry ◽

10.1016/b978-0-08-044304-1.50280-x ◽

2003 ◽

pp. 288

Author(s):

Lydia Pérez ◽

Leticia Quintero ◽

Cecilia Anaya Parrodi ◽

Eusebio Juaristi

Keyword(s):

Michael Addition ◽

Addition Reactions ◽

ChemInform Abstract: Asymmetric Michael Addition Reactions Between 3-Substituted Benzofuran-2(3H)-ones and 1,1-Bis(phenylsulfonyl)ethylene Catalyzed by Bifunctional Catalysts Containing Tertiary Amine and Thiourea Groups.

ChemInform ◽

10.1002/chin.201233112 ◽

2012 ◽

Vol 43 (33) ◽

pp. no-no

Author(s):

Xin Li ◽

Yue-Yan Zhang ◽

Xiao-Song Xue ◽

Jia-Lu Jin ◽

Bo-Xuan Tan ◽

...

Keyword(s):

Tertiary Amine ◽

Michael Addition ◽

Addition Reactions ◽

Bifunctional Catalysts ◽

ChemInform Abstract: The Asymmetric Michael Addition Reactions Using Chiral Imines: Application to the Synthesis of Compounds of Biological Interest

ChemInform ◽

10.1002/chin.199641281 ◽

2010 ◽

Vol 27 (41) ◽

pp. no-no

Author(s):

J. D'ANGELO ◽

C. CAVE ◽

D. DESMAELE ◽

F. DUMAS

Keyword(s):

Michael Addition ◽

Addition Reactions ◽

Biological Interest ◽

Chiral Imines

Biomimetic asymmetric Michael addition reactions in water catalyzed by amino-containing β-cyclodextrin derivatives

Chinese Journal of Catalysis ◽

10.1016/s1872-2067(15)61122-6 ◽

2016 ◽

Vol 37 (8) ◽

pp. 1227-1234 ◽

Cited By ~ 5

Author(s):

Qingying Zhu ◽

Haimin Shen ◽

Zhujin Yang ◽

Hongbing Ji

Keyword(s):

Michael Addition ◽

Addition Reactions ◽

Cyclodextrin Derivatives ◽

Asymmetric Michael addition reactions using ethyl (S)-4,4-dimethylpyroglutamate as a chiral auxiliary

Tetrahedron Letters ◽

10.1016/s0040-4039(98)02648-3 ◽

1999 ◽

Vol 40 (8) ◽

pp. 1575-1578 ◽

Cited By ~ 13

Author(s):

Jesús Ezquerra ◽

Lourdes Prieto ◽

Carmen Avendaño ◽

José Luis Martos ◽

Elena de la Cuesta

Keyword(s):

Michael Addition ◽

Chiral Auxiliary ◽

Addition Reactions ◽

One-Step Stereocontrol of Three Contiguous Stereogenic Centers in Acyclic Systems: The Tuning Effect of an Additive in a Tandem Asymmetric Michael Addition and Meerwein–Ponndorf–Verley Reduction

Angewandte Chemie International Edition ◽

10.1002/anie.200351915 ◽

2003 ◽

Vol 42 (37) ◽

pp. 4515-4517 ◽

Cited By ~ 25

Author(s):

Kiyoharu Nishide ◽

Minoru Ozeki ◽

Hideaki Kunishige ◽

Yukihiro Shigeta ◽

Pranab K. Patra ◽

...

Keyword(s):

Michael Addition ◽

Stereogenic Centers ◽

One Step

ChemInform Abstract: Asymmetric Michael Addition Reactions of Fluoro Carbons

ChemInform ◽

10.1002/chin.200018207 ◽

2010 ◽

Vol 31 (18) ◽

pp. no-no

Author(s):

Takashi Yamazaki

Keyword(s):

Michael Addition ◽

Addition Reactions ◽

Pyrrolidine-based chiral pyridinium ionic liquids (ILs) as recyclable and highly efficient organocatalysts for the asymmetric Michael addition reactions

Tetrahedron Letters ◽

10.1016/j.tetlet.2007.12.024 ◽

2008 ◽

Vol 49 (7) ◽

pp. 1249-1252 ◽

Cited By ~ 103

Author(s):

Bukuo Ni ◽

Qianying Zhang ◽

Allan D. Headley

Keyword(s):

Ionic Liquids ◽

Michael Addition ◽

Addition Reactions ◽

Highly Efficient ◽