Hydroxylamines and Sulfinamide as Amine Components in the Petasis Boronic Acid—Mannich Reaction: Synthesis of N-Hydroxy or Alkoxy-α-aminocarboxylicacids and N-(tert-Butyl sulfinyl)-α-amino Carboxylicacids.

ChemInform ◽  
2004 ◽  
Vol 35 (10) ◽  
Author(s):  
Dinabandhu Naskar ◽  
Amrita Roy ◽  
William L. Seibel ◽  
David E. Portlock
2020 ◽  
Vol 17 ◽  
Author(s):  
Duc Dau Xuan

: The synthesis of the A-B bicyclic ring structure 3 of the natural product Stemocurtisine is described. The synthesis was accomplished in seven synthetic steps from commercially available L-glutamic acid. The key step involved a borono-Mannich reaction between the hemiaminal 6 and trans-β-styryl boronic acid and trans-β-styrylpotassiumtrifluoroborate to prepare the cis diene 4. Attempts to prepare the A-B-C ring compound 2 via intramolecular epoxide ring opening followed by rearangement under different basic conditions were unsuccessful. Only unreactive starting material was recovered.


RSC Advances ◽  
2017 ◽  
Vol 7 (80) ◽  
pp. 50955-50960 ◽  
Author(s):  
A. V. Smolobochkin ◽  
A. S. Gazizov ◽  
A. S. Melyashova ◽  
J. K. Voronina ◽  
A. G. Strelnik ◽  
...  

A novel tandem reaction, which transforms N-(4,4-diethoxybutyl)imines to 3-arylidene-1-pyrrolines via intramolecular Mannich reaction/[1,3]-sigmatropic rearrangement of the aryl fragment is described.


2019 ◽  
Vol 25 (1) ◽  
pp. 47-51 ◽  
Author(s):  
Song Bai ◽  
Yunying Zhu ◽  
Qin Wu

AbstractA series of novel chiral 5-(substituted aryl)-1,3,4-thiadiazole derivatives was synthesized in an enantioselective three-component Mannich reaction using cinchona alkaloid squaramide catalyst with excellent enantioselectivities (up to >99% enantiomeric excess (ee)). The bioassay results showed that these derivatives possessed good to excellent activities against tobacco mosaic virus (TMV).


Tetrahedron ◽  
2017 ◽  
Vol 73 (11) ◽  
pp. 1503-1510 ◽  
Author(s):  
Viktor Ilkei ◽  
András Spaits ◽  
Anita Prechl ◽  
Judit Müller ◽  
Árpád Könczöl ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 41 (19) ◽  
Author(s):  
Michael V. Shevchuk ◽  
Alexander E. Sorochinsky ◽  
Volodymyr P. Khilya ◽  
Vadim D. Romanenko ◽  
Valery P. Kukhar

ChemInform ◽  
2013 ◽  
Vol 44 (43) ◽  
pp. no-no
Author(s):  
Stephen G. Pyne ◽  
Andrew S. Davis ◽  
Thunwadee Ritthiwigrom ◽  
Christopher W. G. Au ◽  
Kongdech Savaspun ◽  
...  

2018 ◽  
Vol 3 (29) ◽  
pp. 8501-8504 ◽  
Author(s):  
Chengliang Feng ◽  
Bin Yan ◽  
Wenjin Yao ◽  
Junqing Chen ◽  
Min Ji

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