Microwave-Sensitive Foamable Poly(ionic liquids) Bearing tert -Butyl Ester Groups: Influence of Counterions on the Ester Pyrolysis

2008 ◽  
Vol 30 (2) ◽  
pp. 94-98 ◽  
Author(s):  
Sadik Amajjahe ◽  
Helmut Ritter
Synlett ◽  
2020 ◽  
Vol 32 (01) ◽  
pp. 45-50
Author(s):  
Udo Nubbemeyer ◽  
Analuisa Nava ◽  
Lukas Trippe ◽  
Andrea Frank ◽  
Lars Andernach ◽  
...  

AbstractStarting from methyl cycloheptatrienyl-1-carboxylate, 6-acylation was successfully achieved employing glutaryl chloride in the presence of AlCl3 under controlled reaction conditions to furnish keto carboxylic acid product. After protection of this keto carboxylic acid as tert-butyl ester, reagent-controlled enantioselective reductions delivered configuration-defined methyl-6-hydroxylalkyl cycloheptatriene-1-carboxylates with up to 80% ee. Whereas simple NaBH4 reduction of the keto carboxylic acid and subsequent lactonization afforded a methyl-6-tetrahydropyranonyl cycloheptatriene-1-carboxylate. Resolution using chiral HPLC delivered the product enantiomers with up to >99% ee Finally, ECD analyses enabled structure elucidation. The products are used as key intermediates in enantioselective 6,11-methylene-lipoxin B4 syntheses.


1993 ◽  
Vol 34 (46) ◽  
pp. 7409-7412 ◽  
Author(s):  
Pierre Chevallet ◽  
Patrick Garrouste ◽  
Barbara Malawska ◽  
Jean Martinez

2014 ◽  
Vol 229 (2) ◽  
pp. 127-128 ◽  
Author(s):  
Chuanhong Zhang ◽  
Jianguo Lin ◽  
Gaochao Lv ◽  
Yang Cao ◽  
Shineng Luo

Abstract C22H23N3O4, triclinic, P1¯ (no. 2), a = 6.992(3) Å, b = 8.159(4) Å, c = 18.778(8) Å, α = 92.118(7)°, β = 93.463(7)°, γ = 101.623(7)°, V = 1045.9 Å3, Z = 2, Rgt(F) = 0.0576, wRref(F2) = 0.1778, T = 296 K.


ChemInform ◽  
2015 ◽  
Vol 46 (24) ◽  
pp. no-no
Author(s):  
Ierasia Triandafillidi ◽  
Aikaterini Bisticha ◽  
Errika Voutyritsa ◽  
Gerasimia Galiatsatou ◽  
Christoforos G. Kokotos

2019 ◽  
Vol 671 ◽  
pp. 127-133 ◽  
Author(s):  
Jun-Cheng Jiang ◽  
Li Li ◽  
Jia-Jia Jiang ◽  
Yan Wang ◽  
Siu-Ming Lo ◽  
...  

ChemInform ◽  
2001 ◽  
Vol 32 (3) ◽  
pp. no-no
Author(s):  
Takashi Ooi ◽  
Minoru Kameda ◽  
Hidenori Tannai ◽  
Keiji Maruoka

Sign in / Sign up

Export Citation Format

Share Document