Reaction modeling of urethane polyols using fraction primary secondary and hindered-secondary hydroxyl content

2014 ◽  
Vol 131 (12) ◽  
pp. n/a-n/a ◽  
Author(s):  
Rima Ghoreishi ◽  
Yusheng Zhao ◽  
Galen J. Suppes
ACS Omega ◽  
2019 ◽  
Vol 4 (1) ◽  
pp. 932-939 ◽  
Author(s):  
Joseph C. Tilly ◽  
Amulya K. Pervaje ◽  
David L. Inglefield ◽  
Erik E. Santiso ◽  
Richard J. Spontak ◽  
...  

2021 ◽  
Vol 566 ◽  
pp. 120906
Author(s):  
Changfu Xu ◽  
Cheng Zheng ◽  
Jiaxin Li ◽  
Ying Liu ◽  
Lizhong Sun

Grana ◽  
1970 ◽  
Vol 10 (3) ◽  
pp. 246-247 ◽  
Author(s):  
P. Fawcett ◽  
D. Green ◽  
R. Holleyhead ◽  
G. Shaw
Keyword(s):  

1985 ◽  
Vol 63 (4) ◽  
pp. 993-995 ◽  
Author(s):  
Kazimierz Antczak ◽  
John F. Kingston ◽  
Alex G. Fallis

Stereoselective total synthesis of (±)-sinularene and (±)-5-epi-sinularene are described. The sequence employs a "blocked" cyclopentadiene in which the cyclopropane unit also serves as a latent methyl group. Thus intramolecular [4 + 2] cycloaddition of the substituted methyl spiro[2.4]hepta-4,6-dien-1-yl)-2-pentenoate 11 affords 5-benzyloxy-6-isopropyl-8-carbomethoxytetracyclo[5.4.01,7.02,4.02,9]undec-10-ene (12) which after selective hydrogenolysis generates the tricyclo[4.4.01,6.02,8]decane (sinularene) ring system. Removal of the secondary hydroxyl function (Ph3P/CCl4/CH3CN; H2/Pd/C), reduction of the methyl ester (LiAlH4), and introduction of the exocyclic double bond (acetate pyrolysis, 550 °C) completes the synthesis of (±)-sinularene in 14 steps from cyclopentadiene. A parallel series of reactions employing the isopropyl epimer of 12 affords (±)-5-epi-sinularene.


2012 ◽  
Vol 48 (18) ◽  
pp. 2448 ◽  
Author(s):  
Amol M. Vibhute ◽  
Adiyala Vidyasagar ◽  
Saritha Sarala ◽  
Kana M. Sureshan

2013 ◽  
Vol 734-737 ◽  
pp. 2089-2093
Author(s):  
Fan Liu ◽  
Yu Liu ◽  
Jia Chuan Chen ◽  
Zhen Wang

In this Paper the Two-Stage Method of Enzyme-Mild Acidic Hydrolysis was Adopted to Separate Lignin from the APMP and the Modified Pulp Samples.And then Analyze the Lignin Structure Changes of the Modified APMP Lignin by Laccase and LMS(laccase/mediator System). it was Found that no Oxidation Took Place on Carbohydrates in the LMS, and Lignin Cα Hydroxyl Oxidization Produce α Carbonyl and H2O2 Bleaching can also Oxidation of Lignin, make the Conjugate C = α Increase;the Syringyl Structure Hydroxyl Content Increase, the Lignin Structure Macromolecular Side Chain Fracturing; Laccase and LMS Oxidative Degradation Chromophoric Group Unsaturated C = O, which can Improve the Brightness of Pulp and Create Better Conditions for Unbleached Pulp.


2013 ◽  
Vol 96 (9) ◽  
pp. 2987-2993 ◽  
Author(s):  
Jens Adam ◽  
Gabi Klein ◽  
Tobias Lehnert

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