
Journal of Organometallic Chemistry p. 257 - 270 (1983)
Update date:2022-07-30
Topics:
Heinicke, J.
Petrasch, A.
Tzschach, A.
In contrast to arsabenzenes the ?-excess aromatic 1H-1,3-benzazarsoles can be alkylated at the arsenic atom as well as lithiated in positions 1 or 2 without addition of LiN(i-Pr)2 and t-BuLi to the As=C (4p-2p)? bond.Alkylations and acylations of the ambident 1-lithio derivatives and substitution reactions of the 2-lithiobenzazarsole are described and the 1H and 13C NMR data of the compounds obtained are given.
View MoreSHENZHEN PENGCHENG REDSTAR INDUSTRY CO.,LTD
Contact:+86-755-82412922
Address:Room 8066, East Block, Square City, Jiabin Road, Luohu District
Shanghai Massive Chemical Technology Co., Ltd.
website:http://www.massivechem.com/
Contact:+86 21 34943721
Address:Room 435, 4th floor, Building 9, No. 2568 Gudai Road,Minhang District, Shanghai,
Contact:+ 86 512 52491118
Address:1 Fuyu Road, Haiyu TownChangshu, Jiangsu, China
Xi'an HO-SHINE Bio-Technology Co., Ltd
Contact:+86 (29) 8248-5435/18292020086
Address:No.6 Shiyuan Road Xian City Shaanxi Province, 710048 China
Xinchang Jiu Xin Pharmaceutical Co., Ltd
website:http://www.jiuxinpharm.com
Contact:86 137 5756 8585
Address:Poyang industry Park
Doi:10.1002/omr.1270211004
(1983)Doi:10.1248/cpb.31.4417
(1983)Doi:10.1002/ejic.201001165
(2011)Doi:10.1007/bf03246225
(2011)Doi:10.1246/bcsj.79.612
(2006)Doi:10.1021/ja00323a041
(1984)