Intramolecular imine cross-coupling in dibenzylidine sulfamides: Synthesis of unsymmetrical 1,2-diaryl ethanediamines

DOI: 10.1016/0040-4039(96)00406-6

Source and publish data:

Tetrahedron Letters p. 2859 - 2862 (1996)

Update date:2022-07-30

Topics:

Authors:

Pansare, Sunil V.

Malusare, Mahesh G.

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

Article abstract of DOI:10.1016/0040-4039(96)00406-6

Intramolecular reductive cross-coupling of unsymmetrical dibenzylidene sulfamides generates the corresponding cyclic sulfamides in good yield. These intermediates are readily converted to the free, unsymmetrical 1,2-diaryl ethanediamines.

Full text of DOI:10.1016/0040-4039(96)00406-6

Products guided by the article

Product name:C₁₆H₁₆N₂O₂S

Cas No:176858-01-8

R&D Labs maybe for 176858-01-8

Shanghai Balmxy Pharmaceutical Co., Ltd

Contact:0086-21-24206007

Address:Room 402, 15#, No. 909 wangyue Road, shanghai, P. R. China
Dongtai Xinyuan Chemical Co., Ltd.

Contact:+86-21-56733000

Address:404F, 99Nong No.117 Zhongtan Rd. Shanghai
Wuxi Pharma-Trading Import & Export Co.,Ltd.

Contact:+86-510-82304590 82716390

Address:Room 523,Youzu Alliance Building,No.88 Renmin Zhonglu,Wuxi,Jiangsu,China
BIOS CHEMICALS

Contact:+33-5-34012600

Address:28 ZA des Pignès
Anhui Xinyuan Technology Co.,Ltd

Contact:0086-559-3515800

Address:No.16 Zijin Rd, Circular Economic Zone, Huizhou District, Huangshan Anhui China

Relevant to this article

Magic acid free generation of antiaromatic dications at room temperature

Doi:10.1021/jo201512n
(2011)
Photocleavable protecting groups as nucleobase protections allowed the solid-phase synthesis of base-sensitive SATE-prooligonucleotides

Doi:10.1021/jo990479h
(1999)
Synthesis of 3-substituted 4-hydroxyquinolin-2-ones via C-acylation reactions of active methylene compounds with functionalized 3,1-benzoxazin-4- ones

Doi:10.3987/com-99-8508
(1999)
Site-selective labeling of a lysine residue in human serum albumin

Doi:10.1002/anie.201405924
(2014)
A practical method for synthesis of terminal 1,2-diols in high enantiomeric excess via oxazaborolidine-catalyzed asymmetric reduction

Doi:10.1016/S0957-4166(99)00184-6
(1999)
A convergent, stereocontrolled synthesis of C₂-symmetrical and pseudosymmetrical sulfur-tethered bis(amino alcohols)

Doi:10.1016/S0040-4039(99)00568-7
(1999)

Article Doi