CAUSTIC PRETREATMENT STUDY FOR ENZYMATIC HYDROLYSIS OF WHEAT STRAW**Presented at the symposium of Feed, Fuels and Chemicals from Wood and Agricultural Residues, 184th National ACS Meeting, Kansas City, MO., Sept. 12-17, 1982.

Author(s):  
M.M. Gharpuray ◽  
L.T. Fan ◽  
Yong-Hyun Lee
2012 ◽  
Vol 87 (2) ◽  
pp. 1280-1285 ◽  
Author(s):  
Greta Radeva ◽  
Ivo Valchev ◽  
Stoiko Petrin ◽  
Eva Valcheva ◽  
Petya Tsekova

2010 ◽  
Vol 85 (9) ◽  
pp. 1291-1297 ◽  
Author(s):  
Pablo Alvira ◽  
María José Negro ◽  
Felicia Sáez ◽  
Mercedes Ballesteros

2018 ◽  
Vol 102 (22) ◽  
pp. 9831-9842 ◽  
Author(s):  
Mengjie Wu ◽  
Hongyu Liu ◽  
Junyuan Guo ◽  
Chunping Yang

Author(s):  
Douglass Taber

Alkenes are usually reduced by catalytic hydrogenation. Diimide reduction is a mild and neutral alternative. Keith R. Buszek, now at the University of Missouri, Kansas City, has shown (J. Org. Chem. 2007, 72, 3125) that the reduction can conveniently be carried out on resin-bound alkenes, using 2-NBSH (o-nitrobenzenesulfonylhydrazide) with Et3 N for convenient room temperature diimide generation. Ozone can be difficult to dispense accurately on small scale. Masahito Ochiai of the University of Tokushima has uncovered (J. Am. Chem. Soc. 2007, 129, 2772) an alternative, using acid-promoted Ph-I=O. Isolated alkenes also work well. MCPBA is the reagent most commonly used for alkene epoxidation. Payne oxidation (H2O2 /CH3CN) is a convenient and inexpensive alternative. In the course of a study of the enantioselective enzymatic hydrolysis of 6, Takeshi Sugai of Keio University has described (Tetrahedron Lett. 2007, 48, 979) a practical procedure for multigram Payne epoxidation of 5. Several procedures have been put forward for functionalizing terminal alkenes, exemplified by 7. Stefan Grimme and Armido Studer of the Universität Münster have developed (J. Am. Chem. Soc. 2007, 129, 4498) a free radical alkene amination, represented by the conversion of 7 to 9. Tehshik P. Yoon of the University of Wisconsin has found (J. Am. Chem. Soc. 2007, 129, 1866) that Cu catalyzes the addition of oxaziridines such as 10 to alkenes, to make 11. Shinji Nakamura of the University of Tokyo and Masanobu Uchiyama of the University of Tokyo and RIKEN have established (J. Am. Chem. Soc. 2007, 129, 28) that the anion from Cu promoted addition of the silyl zinc reagent to alkenes is long-lived enough to be trapped by electrophiles, including H+ to give 12. Hideki Yorimitsu and Koichiro Oshima of Kyoto University have developed (J. Am. Chem. Soc. 2007, 129, 6094) a complementary transformation, Ni-catalyzed addition of 13 to give 14. The conversion of 7 to 15 reported (Organic Lett. 2007, 9, 53) by Li-Biao Han of the National Institute of Advanced Industrial Science and Technology, Tsukuba, is likely also a free-radical process.


2015 ◽  
Vol 175 ◽  
pp. 75-81 ◽  
Author(s):  
Jinping Zhang ◽  
Wei Liu ◽  
Qingxi Hou ◽  
Junwei Chen ◽  
Ningpan Xu ◽  
...  

RSC Advances ◽  
2014 ◽  
Vol 4 (69) ◽  
pp. 36591-36596 ◽  
Author(s):  
M. H. Sipponen ◽  
V. Pihlajaniemi ◽  
O. Pastinen ◽  
S. Laakso

24 h enzymatic hydrolysis (15 FPU g−1) of solid residues from wheat straw autohydrolysis. Cellulose conversion as a function of lignin content (left) or lignin surface area (right) in solid residues.


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