Recent Advances in Direct Synthesis of Value‐Added Aromatic Chemicals from Syngas by Cascade Reactions over Bifunctional Catalysts

2019 ◽  
Vol 31 (34) ◽  
pp. 1803390 ◽  
Author(s):  
Saravanan Kasipandi ◽  
Jong Wook Bae
2021 ◽  
Vol 28 ◽  
pp. 100433
Author(s):  
Alexandra Del Castillo-Llamosas ◽  
Pablo G. del Río ◽  
Alba Pérez-Pérez ◽  
Remedios Yáñez ◽  
Gil Garrote ◽  
...  

Molecules ◽  
2020 ◽  
Vol 25 (22) ◽  
pp. 5270
Author(s):  
Zhenbo Yuan ◽  
Xuanzhong Liu ◽  
Changmei Liu ◽  
Yan Zhang ◽  
Yijian Rao

Non-proteinogenic amino acids have attracted tremendous interest for their essential applications in the realm of biology and chemistry. Recently, rising C–H functionalization has been considered an alternative powerful method for the direct synthesis of non-proteinogenic amino acids. Meanwhile, photochemistry has become popular for its predominant advantages of mild conditions and conservation of energy. Therefore, C–H functionalization and photochemistry have been merged to synthesize diverse non-proteinogenic amino acids in a mild and environmentally friendly way. In this review, the recent developments in the photo-mediated C–H functionalization of proteinogenic amino acids derivatives for the rapid synthesis of versatile non-proteinogenic amino acids are presented. Moreover, postulated mechanisms are also described wherever needed.


2009 ◽  
Vol 111 (8) ◽  
pp. 788-799 ◽  
Author(s):  
Mario Pagliaro ◽  
Rosaria Ciriminna ◽  
Hiroshi Kimura ◽  
Michele Rossi ◽  
Cristina Della Pina

Author(s):  
Yoo Seok Lee ◽  
Koun Lim ◽  
Shelley D. Minteer

Enzyme cascades are plentiful in nature, but they also have potential in artificial applications due to the possibility of using the target substrate in biofuel cells, electrosynthesis, and biosensors. Cascade reactions from enzymes or hybrid bioorganic catalyst systems exhibit extended substrate range, reaction depth, and increased overall performance. This review addresses the strategies of cascade biocatalysis and bioelectrocatalysis for ( a) CO2 fixation, ( b) high value-added product formation, ( c) sustainable energy sources via deep oxidation, and ( d) cascaded electrochemical enzymatic biosensors. These recent updates in the field provide fundamental concepts, designs of artificial electrocatalytic oxidation-reduction pathways (using a flexible setup involving organic catalysts and engineered enzymes), and advances in hybrid cascaded sensors for sensitive analyte detection. Expected final online publication date for the Annual Review of Physical Chemistry, Volume 72 is April 2021. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.


ChemCatChem ◽  
2018 ◽  
Vol 11 (1) ◽  
pp. 298-308 ◽  
Author(s):  
Richard J. Lewis ◽  
Graham J. Hutchings

2019 ◽  
Vol 58 (35) ◽  
pp. 15872-15901 ◽  
Author(s):  
Daniela Xulú Martínez-Vargas ◽  
Ladislao Sandoval-Rangel ◽  
Omar Campuzano-Calderon ◽  
Michel Romero-Flores ◽  
Francisco J. Lozano ◽  
...  

2020 ◽  
Vol 7 (20) ◽  
pp. 3266-3283
Author(s):  
Yu Wang ◽  
Da-Ming Du

In this review, we summarized recent advances in organocatalytic asymmetric oxa-Michael addition triggered cascade reactions.


2018 ◽  
Vol 243 ◽  
pp. 00002
Author(s):  
Olga Vodorezova ◽  
Pavel Musich ◽  
Natalia Karakchieva ◽  
Lothar Heinrich ◽  
Irina Kurzina

Dimethyl ether (DME) can be used as a replacement for diesel fuel in transportation. The catalytic effectiveness of bifunctional catalysts for DME one-stage synthesis from carbon monoxide and hydrogen was estimated in the paper. Bifunctional catalysts CuZnAl/HZSM-5, CuZnAlCr/HZSM-5, and CuZnAlZr/HZSM-5 were obtained by physical mixing of CuZnAl(Cr/Zr)– Ох and HZSM-5 components and were characterized by BET, X-ray diffraction, and temperatureprogrammed surface reaction methods. Based on the TPSR results, the mechanism of the interaction of methanol and DME with the surface of the bifunctional catalyst was studied. It was found that the temperature range of the greatest catalytic activity was 240–260 °С.


Sign in / Sign up

Export Citation Format

Share Document