Preparation of N-alkyl Pyrrolidinones via Photocyclization of γ-Keto-α,β-Unsaturated Amides

DOI: 10.1016/0040-4039(95)00779-C

Source and publish data:

Tetrahedron Letters p. 4197 - 4200 (1995)

Update date:2022-08-03

Topics:

Authors:

Dittami, James P.

Xu, Feng

Qi, Hua Qi, Hua

Martin, Matthew W.

Bordner, Jon

et al. et al.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/0040-4039(95)00779-C

Photolysis of γ-keto-α,β-unsaturated amides provides N-alkyl pyrrolidinones in high yield (77-100percent).The procedure is applicable to a variety of amides derived from the corresponding γ-keto acid.

Full text of DOI:10.1016/0040-4039(95)00779-C

Products guided by the article

Product name:(E)-N-benzyl-4-oxopent-2-enamide

Cas No:169170-51-8

R&D Labs maybe for 169170-51-8

SYN Pharma Co., Ltd

Contact:86-21 60347964

Address:No.1304, West Meilong Road, Minhang District, Shanghai, China
hangzhou verychem science and technology co.ltd

website:http://www.verypharm.com

Contact:+86-571-88162785; 88162786

Address:F1502, 753 Shenhua road, Hangzhou, China
Taizhou Chenyi chemical co. LTD,

Contact:13736652831

Address:NO.273 SHANGHAI SOUTH STREET,LUQIAO DISTRICT,ZHEJIANG PROVINCE,CHINA.
Wuhan Chemchemical Co., Ltd.(expird)

Contact:15973022782

Address:7-5-6218,Incubation Centre,Guandong Industry Park, East Lake High-Tech Development Zone,Wuhan City.
Fujian Huitian Biological Pharmacy Co., Ltd.

Contact:0086-598-8300831; 8339920

Address:No.46,Taijiang Road,Sanming City,Fujian,China

Relevant to this article

Novel cytotoxic 3'-(tert-butyl) 3'-dephenyl analogs of paclitaxel and docetaxel

Doi:10.1021/jm00019a012
(1995)
2-[(substituted)phenyl]-5-[1-(2-phenylazacycloheptyl) methyl]-1H-pyrroles with high affinity and selectivity for the dopamine D₃ receptor

Doi:10.1016/S0960-894X(97)00045-0
(1997)
The synthesis, structure and reactivity of aldehyde substituted η³-allylic complexes of molybdenum

Doi:10.1016/S0022-328X(97)00542-1
(1998)
Kinetic and Thermodynamic Studies of Iron(III) and Iron(IV)σ -Bonded Porphyrins. Formation and Reactivity of [(OEP)Fe(R)]ⁿ⁺, Where OEP Is the Dianion of Octaethylporphyrin (n = 0, 1, 2, 3) and R = C₆H₅, 3,4,5-C₆F₃H₂, 2,4,6-C₆F₃₂, C₆F₄H, or C₆F₅

Doi:10.1021/ic9714706
(1998)
Enantioselective inclusion of pyrene-1-sulfonate salts of α-amino acids with crystals of α-cyclodextrin

Doi:10.1016/j.tet.2020.131100
(2020)
Analogues of azepinomycin as inhibitors of guanase

Doi:10.1080/07328319808004227
(1998)

Article Doi