Journal of the Chemical Society. Chemical communications p. 1164 - 1166 (1983)
Update date:2022-08-03
Topics:
Horton, Derek
Machinami, Tomoya
Takagi, Yasushi
Bergmann, Carl W.
Christoph, Gary C.
Acyclic unsaturated sugars obtained by Wittig extension of aldehydo arabinose precursors undergo stereoselective Diels-Alder addition of cyclopentadiene, permitting isolation of a single, crystalline, optically pure norbornene adduct whose stereochemistry may be controlled by the enantiomeric form of the sugar used and the conditions of the cycloaddition reaction.
View MoreShanghai Haoyuan Chemexpress Co., Ltd.
website:https://www.chemexpress.com/
Contact:86-21-58950125
Address:No.3 Building, No.1999, Zhangheng Road, ZhangjiangHighTech Park, Shanghai, P.R.China,201203
ShangHai Soyoung Biotechnology Inc
website:http://www.soyoungbio.com
Contact:+86-21-69893009
Address:shanghai
Tianjin Tongde Biological Technology Co., Ltd.
Contact:86-22-23309138
Address:Room 402, bulidingE3 Detection certification park, XiQingDistrict, Tianjin City
Shanghai Rich Chemicals Co., Ltd
website:http://www.richchemical.com
Contact:+86-21-20255798
Address:Pudong Shanghai,China
Nanjing distinctions Medical Technology Co., Ltd.(expird)
Contact:+86-15996203785 13914714059
Address:nanjing,jiangsu , China
Doi:10.1016/0040-4020(89)80034-1
(1989)Doi:10.1002/hlca.19360190154
(1936)Doi:10.1080/07391102.2020.1804459
(2021)Doi:10.1021/jm020210h
(2002)Doi:10.1021/ja01162a543
(1950)Doi:10.1016/S0968-0896(02)00108-6
(2002)
