ChemInform Abstract: Domino-Reaction of Oxal(imidoyl)chlorides with 3-Aminoisoxazoles: Regio- and Stereoselective Synthesis of 1,4-Dihydro-imidazo[4,5-b]quinoxalines.

ChemInform ◽  
2010 ◽  
Vol 30 (31) ◽  
pp. no-no
Author(s):  
Joerg Wuckelt ◽  
Manfred Doering ◽  
Peter Langer ◽  
Rainer Beckert
Keyword(s):  
Stereoselective Synthesis ◽  
Domino Reaction ◽  
Imidoyl Chlorides

Domino-Reaction of Oxal(imidoyl)chlorides with 3-Aminoisoxazoles: Regio- and Stereoselective Synthesis of 1,4-Dihydro-imidazo[4,5-b]quinoxalines

Synlett ◽  
1999 ◽  
Vol 1999 (4) ◽  
pp. 468-470 ◽  
Author(s):  
Jörg Wuckelt ◽  
Manfred Döring ◽  
Peter Langer ◽  
Rainer Beckert
Keyword(s):  
Stereoselective Synthesis ◽  
Domino Reaction ◽  
Imidoyl Chlorides

scholarly journals An Enamide‐Based Domino Reaction for a Highly Stereoselective Synthesis of Tetrahydropyrans

2019 ◽  
Vol 58 (37) ◽  
pp. 13056-13059 ◽  
Author(s):  
Philipp Kramer ◽  
Jennifer Grimmer ◽  
Michael Bolte ◽  
Georg Manolikakes
Keyword(s):  
Stereoselective Synthesis ◽  
Domino Reaction

Intercepting the Nazarov Oxyallyl Intermediate with α-Formyl­vinyl Anion Equivalents to Access Formal Morita–Baylis–Hillman Alkylation Products

Synlett ◽  
2017 ◽  
Vol 28 (12) ◽  
pp. 1486-1490 ◽  
Author(s):  
F. West ◽  
Yen-Ku Wu ◽  
Rongrong Lin
Keyword(s):  
Lewis Acid ◽  
Stereoselective Synthesis ◽  
Domino Reaction ◽  
Alkylation Process ◽  
Acid Catalyzed

A Lewis acid catalyzed cationic domino reaction involving sequential electrocyclization and polar addition of allenol ethers onto the resulting oxyallyl species is described. The overall sequence allows a highly stereoselective synthesis of densely substituted cyclopentanoid compounds containing α-formylvinyl functionality which is formally equivalent to products of a Morita–Baylis–Hillman alkylation process.

ChemInform Abstract: Regio- and Stereoselective Synthesis of Benzothiazolo-Pyrimidinones via an NHC-Catalyzed Mannich/Lactamization Domino Reaction.

ChemInform ◽  
2015 ◽  
Vol 46 (24) ◽  
pp. no-no
Author(s):  
Qijian Ni ◽  
Xiaoxiao Song ◽  
Jiawen Xiong ◽  
Gerhard Raabe ◽  
Dieter Enders
Keyword(s):  
Stereoselective Synthesis ◽  
Domino Reaction

Palladium-Catalyzed Domino Reaction for Stereoselective Synthesis of Multisubstituted Olefins: Construction of Blue Luminogens

2018 ◽  
Vol 83 (8) ◽  
pp. 4441-4454 ◽  
Author(s):  
Tao-Tao Hao ◽  
Hao-Ran Liang ◽  
Ying-Han Ou-Yang ◽  
Chang-Zhen Yin ◽  
Xue-Li Zheng ◽  
...  
Keyword(s):  
Stereoselective Synthesis ◽  
Domino Reaction ◽  
Palladium Catalyzed

Unique Michael Addition-Initiated Domino Reaction for the Stereoselective Synthesis of Functionalized Macrolactones from α-Nitroketones in Water†

2005 ◽  
Vol 7 (11) ◽  
pp. 2197-2200 ◽  
Author(s):  
Giorgio Giorgi ◽  
Sonia Miranda ◽  
Pilar López-Alvarado ◽  
Carmen Avendaño ◽  
Jean Rodriguez ◽  
...  
Keyword(s):  
Michael Addition ◽  
Stereoselective Synthesis ◽  
Domino Reaction

scholarly journals Stereoselective synthesis of chromane derivatives via a domino reaction catalyzed by modularly designed organocatalysts

2019 ◽  
Vol 17 (1) ◽  
pp. 151-155 ◽  
Author(s):  
Satish Jakkampudi ◽  
Ramarao Parella ◽  
John C.-G. Zhao
Keyword(s):  
Stereoselective Synthesis ◽  
Domino Reaction ◽  
Diastereoselective Synthesis

A highly enantio- and diastereoselective synthesis of functionalized chroman-2-ones and chromanes was achieved.

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