Enantioselective One-Pot Two-Step Synthesis of Hydrophobic Allylic Alcohols in Aqueous Medium through the Combination of a Wittig Reaction and an Enzymatic Ketone Reduction

2007 ◽  
Vol 2007 (31) ◽  
pp. 5175-5179 ◽  
Author(s):  
Marina Kraußer ◽  
Werner Hummel ◽  
Harald Gröger
Keyword(s):  
Aqueous Medium ◽  
Wittig Reaction ◽  
Allylic Alcohols ◽  
One Pot ◽  
Ketone Reduction

The One-Pot Palladium Catalyzed Wittig Reaction with Allylic Alcohols. Scope and Limitations

1986 ◽  
Vol 16 (9) ◽  
pp. 1003-1013 ◽  
Author(s):  
M. Moreno-Mañas ◽  
R. M. Ortuño ◽  
M. Prat ◽  
M. A. Galán
Keyword(s):  
Wittig Reaction ◽  
Allylic Alcohols ◽  
One Pot ◽  
Palladium Catalyzed ◽  
The One

Chemoenzymatic one-pot synthesis in an aqueous medium: combination of metal-catalysed allylic alcohol isomerisation–asymmetric bioamination

2015 ◽  
Vol 51 (54) ◽  
pp. 10937-10940 ◽  
Author(s):  
Nicolás Ríos-Lombardía ◽  
Cristian Vidal ◽  
María Cocina ◽  
Francisco Morís ◽  
Joaquín García-Álvarez ◽  
...  
Keyword(s):  
Aqueous Medium ◽  
Allylic Alcohol ◽  
Allylic Alcohols ◽  
One Pot ◽  
One Pot Synthesis ◽  
First Time

The ruthenium-catalysed isomerisation of allylic alcohols was coupled, for the first time, with asymmetric bioamination in a one-pot process in an aqueous medium.

A Facile One-Pot and Green Multi-Component Synthesis of 2-Amino-4Hpyrans Promoted by Pyridinium p-Toluenesulfonate in Aqueous Medium

2016 ◽  
Vol 13 (7) ◽  
pp. 482-490 ◽  
Author(s):  
Chaima Boureghda ◽  
Imène Amine Khodja ◽  
Bertrand Carboni ◽  
Raouf Boulcina ◽  
Oumeima Kermiche ◽  
...  
Keyword(s):  
Aqueous Medium ◽  
One Pot

Iodine Catalyzed Highly Efficient One Pot Three Component Synthesis of 4-arylidene-3-methylisoxazol-5 (4H) -one in Aqueous Medium

2018 ◽  
Vol 5 (2) ◽  
pp. 122-128 ◽  
Author(s):  
Srinivas L. Nakkalwar ◽  
Shivaji B. Patwari ◽  
Mohasim M. Patel ◽  
Vivekanand B. Jadhav
Keyword(s):  
Aqueous Medium ◽  
One Pot ◽  
Highly Efficient

ChemInform Abstract: Nanodomain Cubic Cuprous Oxide as Reusable Catalyst in One-Pot Synthesis of 3-Alkyl/Aryl-3- (pyrrole-2-yl/indole-3-yl)-2-phenyl-2,3-dihydro-isoindolinones in Aqueous Medium.

ChemInform ◽  
2014 ◽  
Vol 45 (41) ◽  
pp. no-no
Author(s):  
Swarbhanu Sarkar ◽  
Nivedita Chatterjee ◽  
Manas Roy ◽  
Rammyani Pal ◽  
Sabyasachi Sarkar ◽  
...  
Keyword(s):  
Aqueous Medium ◽  
Cuprous Oxide ◽  
Reusable Catalyst ◽  
One Pot ◽  
Alkyl Aryl ◽  
One Pot Synthesis

scholarly journals Tandem oxidation–Wittig reaction using nanocrystalline barium manganate (BaMnO4); an improved one-pot protocol

2016 ◽  
Vol 57 (33) ◽  
pp. 3773-3775 ◽  
Author(s):  
Mohammad Gholinejad ◽  
Habib Firouzabadi ◽  
Maedeh Bahrami ◽  
Carmen Nájera
Keyword(s):  
Wittig Reaction ◽  
One Pot

A Domino Heck Coupling–Cyclization–Dehydrogenative Strategy for the One-Pot Synthesis of Quinolines

Synthesis ◽  
2021 ◽  
Author(s):  
Santanu Ghora ◽  
Chinnabattigalla Sreenivasulu ◽  
Gedu Satyanarayana
Keyword(s):  
Functional Group ◽  
Exchange Process ◽  
Palladium Catalysis ◽  
Allylic Alcohols ◽  
Heck Coupling ◽  
One Pot ◽  
Synthetic Process ◽  
Intramolecular Condensation ◽  
The One

AbstractAn efficient, one-pot, domino synthesis of quinolines via the coupling of iodoanilines with allylic alcohols facilitated by palladium catalysis is described. The overall synthetic process involves an intermolecular Heck coupling between 2-iodoanilines and allylic alcohols, intramolecular condensation of in situ generated ketones with an internal amine functional group, and a dehydrogenation sequence. Notably, this protocol occurs in water as a green solvent. Significantly, the method exhibits broad substrate scope and is applied for the synthesis of deuterated quinolines through a deuterium-exchange process.

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