Formamidinesulfinic acid reduction of dihydrocodeinone derivatives

DOI: 10.1021/jo00402a016

Source and publish data:

Journal of Organic Chemistry p. 1555 - 1557 (1978)

Update date:2022-08-05

Topics: Reagents Work-Up Stir and Heat (if necessary) Analysis and Characterization

Authors:

Brine Brine

Boldt Boldt

Coleman Coleman

et al. et al.

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

Article abstract of DOI:10.1021/jo00402a016

Treatment of dihydrocodeinone (1f) with formamidinesulfinic acid afforded mixtures of dihydrothebainone (3a) dihydroisothebainol dihydroisothenainol (4a) under both homogeneous and heterogeneous conditions. Similar treatment of 14-hydroxydihydrocodeinone

Full text of DOI:10.1021/jo00402a016

Products guided by the article

Product name:7,8-Dihydrothebainon

Cas No:88196-19-4

R&D Labs maybe for 88196-19-4

Winchem Industrial Co. Ltd.(expird)

Contact:86-574-83851061 86-574-87083208

Address:Room 905, No.3 Building,East Business Center, 456 Xingning Road, Ningbo City,China
Hefei EnliPharma Tecnology Co.,Ltd

Contact:0086-551-66399836

Address:Qing Cheng ShuiXiang Building 805, Mengcheng North Road , ShuangFeng Economic Development Zone Anhui HeFei
ZCIC INTERNATIONAL LTD

Contact:+86-512-56795332

Address:No227 Shuanglong Rd, Fenghuang, Zhangjiagang
Santow Laboratory Limited

Contact:+86-371-55981030

Address:Room 1571, Macalline Soho, No.1, Shangdu Road, Zhengzhou, Henan
Tosta Enterprise Co., Ltd.

Contact:+86-134-5286-9121

Address:Add: Wing Tuck Commercial Centre, 177-183 Wing Lok Street, Hong Kong,

Relevant to this article

Comparative Structure-Activity Relationships of Antifolate Triazines Inhibiting Murine Tumor Cells Sensitive and Resistant to Methotrexate

Doi:10.1021/jm00369a019
(1984)
Cyclisation of α-(2-mercaptobenzoyl)- and α-(2-aminobenzoyl)lactames; Synthesis of benzothiopyranopyrrolinones and pyrrolinoquinolinones

Doi:10.1002/ardp.19833161102
(1983)
Design, synthesis, and biological evaluation of pyrimidine-2-carboxamide analogs: Investigation for novel RAGE inhibitors with reduced hydrophobicity and toxicity

Doi:10.1007/s12272-015-0596-5
(2015)
Preparative resolution of a key intermediate for the synthesis of optically active m-phenylene PGI₂ derivatives

Doi:10.1016/S0957-4166(99)00442-5
(1999)
Kinetic and thermodynamic aspects of the regioselective addition of bifunctional hydroxylaminooxime-type HO-nucleophiles to Pt-complexed nitriles

Doi:10.1021/ic051909r
(2006)
2-Benzazepines. 7. Synthesis of pyrimido[5,4-d][2]benzazepines [1]

Doi:10.1002/jhet.5570200512
(1983)

Article Doi