ChemInform Abstract: Highly Stereoselective Synthesis of Trisubstituted Cyclohexanols Using a Guanidine-Catalyzed Tandem Henry-Michael Reaction.

Qipu Dai; Huicai Huang; John Cong-Gui Zhao

doi:10.1002/chin.201335087

ChemInform Abstract: Highly Stereoselective Synthesis of Trisubstituted Cyclohexanols Using a Guanidine-Catalyzed Tandem Henry-Michael Reaction.

ChemInform ◽

10.1002/chin.201335087 ◽

2013 ◽

Vol 44 (35) ◽

pp. no-no

Author(s):

Qipu Dai ◽

Huicai Huang ◽

John Cong-Gui Zhao

Keyword(s):

Stereoselective Synthesis ◽

Michael Reaction

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ChemInform Abstract: The Mukaiyama-Michael Reaction of N-Acyl-2,3-dihydro-4-pyridones: Regio- and Stereoselective Synthesis of cis-2,6-Disubstituted 1,2,5,6-Tetrahydropyridines.

ChemInform ◽

10.1002/chin.199952150 ◽

2010 ◽

Vol 30 (52) ◽

pp. no-no

Author(s):

Jeffrey T. Kuethe ◽

Daniel L. Comins

Keyword(s):

Stereoselective Synthesis ◽

Michael Reaction

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Stereoselective Synthesis of 4′‐Selenonucleosides via the Seleno‐Michael Reaction

Current Protocols in Nucleic Acid Chemistry ◽

10.1002/cpnc.27 ◽

2017 ◽

Vol 69 (1) ◽

Author(s):

Pramod K. Sahu ◽

Dnyandev B. Jarhad ◽

Gyudong Kim ◽

Lak Shin Jeong

Keyword(s):

Stereoselective Synthesis ◽

Michael Reaction

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ChemInform Abstract: Stereoselective Synthesis of Indanylglycine Derivatives by a Tandem Michael-Michael Reaction.

ChemInform ◽

10.1002/chin.201313076 ◽

2013 ◽

Vol 44 (13) ◽

pp. no-no

Author(s):

Angela Rincon ◽

Vanesa Carmona ◽

M. Rosario Torres ◽

Aurelio G. Csaky

Keyword(s):

Stereoselective Synthesis ◽

Michael Reaction

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Stereoselective Synthesis of 2,6-cis-Tetrahydropyrans through a Tandem Allylic Oxidation/Oxa-Michael Reaction Promoted by thegem-Disubstituent Effect: Synthesis of (+)-Neopeltolide Macrolactone

Angewandte Chemie ◽

10.1002/ange.200903690 ◽

2009 ◽

Vol 121 (41) ◽

pp. 7713-7717 ◽

Cited By ~ 18

Author(s):

Hyoungsu Kim ◽

Yongho Park ◽

Jiyong Hong

Keyword(s):

Stereoselective Synthesis ◽

Michael Reaction ◽

Allylic Oxidation

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ChemInform Abstract: Broensted Acid Catalyzed Condensation-Michael Reaction-Pictet-Spengler Cyclization - Highly Stereoselective Synthesis of Indoloquinolizidines.

ChemInform ◽

10.1002/chin.201151147 ◽

2011 ◽

Vol 42 (51) ◽

pp. no-no

Author(s):

Magnus Rueping ◽

Chandra M. R. Volla

Keyword(s):

Stereoselective Synthesis ◽

Michael Reaction ◽

Acid Catalyzed

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Brønsted-acid catalyzed condensation-Michael reaction-Pictet–Spengler cyclization—highly stereoselective synthesis of indoloquinolizidines

RSC Advances ◽

10.1039/c1ra00305d ◽

2011 ◽

Vol 1 (1) ◽

pp. 79 ◽

Cited By ~ 27

Author(s):

Magnus Rueping ◽

Chandra M. R. Volla

Keyword(s):

Stereoselective Synthesis ◽

Michael Reaction ◽

Bronsted Acid ◽

Brønsted Acid ◽

Brönsted Acid ◽

Acid Catalyzed

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ChemInform Abstract: Stereoselective Synthesis of Spirooxindole Derivatives Using an Organocatalyzed Tandem Michael-Michael Reaction.

ChemInform ◽

10.1002/chin.201624102 ◽

2016 ◽

Vol 47 (24) ◽

Author(s):

Huicai Huang ◽

Manisha Bihani ◽

John C.-G. Zhao

Keyword(s):

Stereoselective Synthesis ◽

Michael Reaction

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Stereoselective synthesis of trifluoromethyl-substituted 1,2-diamines by aza-Michael reaction with trans-3,3,3-trifluoro-1-nitropropene

Tetrahedron ◽

10.1016/j.tet.2006.06.013 ◽

2006 ◽

Vol 62 (34) ◽

pp. 8109-8114 ◽

Cited By ~ 12

Author(s):

Joël Turconi ◽

Luc Lebeau ◽

Jean-Marc Paris ◽

Charles Mioskowski

Keyword(s):

Stereoselective Synthesis ◽

Michael Reaction

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ChemInform Abstract: NEW STEREOSELECTIVE SYNTHESIS OF 9-METHYL-CIS-DECALIN DERIVATIVES BY DOUBLE MICHAEL REACTION OF 3,5-DIMETHYL-4-METHYLENECYCLOHEX-2-ENONE AND DIMETHYL 3-OXOGLUTARATE; X-RAY CRYSTAL AND MOLECULAR STRUCTURE OF TWO OF THE PRODUCTS

Chemischer Informationsdienst ◽

10.1002/chin.197851163 ◽

1978 ◽

Vol 9 (51) ◽

Author(s):

H. IRIE ◽

J. KATAKAWA ◽

Y. MIZUNO ◽

S. UDAKA ◽

T. TAGA ◽

...

Keyword(s):

Molecular Structure ◽

Stereoselective Synthesis ◽

Michael Reaction ◽

Crystal And Molecular Structure ◽

X Ray

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ChemInform Abstract: Stereoselective Synthesis of 2,6-cis-Tetrahydropyrans Through a Tandem Allylic Oxidation/Oxa-Michael Reaction Promoted by the gem-Disubstituent Effect: Synthesis of (+)-Neopeltolide Macrolactone.

ChemInform ◽

10.1002/chin.201005115 ◽

2010 ◽

Vol 41 (5) ◽

Author(s):

Hyoungsu Kim ◽

Yangho Park ◽

Jiyong Hong

Keyword(s):

Stereoselective Synthesis ◽

Michael Reaction ◽

Allylic Oxidation

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