Tetrahedron Letters p. 6689 - 6692 (1999)
Update date:2022-09-26
Topics:
Coxon, Geoffrey D.
Knobl, Stefan
Roberts, Evan
Baird, Mark S.
Al Dulayymi, Juma R.
Besra, Gurdyal S.
Brennan, Patrick J.
Minnikin, David E.
(11R, 12S)-Lactobacillic acid (1) has been prepared either from D- mannitol by asymmetric cyclopropanation or from cis-cyclopropane-1, 2- dimethanol by enzymatic desymmetrisation. The syntheses of (l1S 12R)- lactobacillic acid (2) and (1R, 2S) 1- (3'-methoxycarbonylpropyl)-2- octadecylcyclopropane (26) and related analogues (27 and 28) have also been achieved.
View Morewebsite:http://www.orchid-chem.com
Contact:+86-571-85395792
Address:607, North Zhongshan Road, Hangzhou 310000 China
ShangHai Original Economy-Trade Develop Co.,Ltd.,
Contact:86-21-68552131
Address:shanghai
Xinjiang Fufeng Biotechnologies Co., Ltd.
Contact:+86-539-7287111
Address:GANQUANPU INDUSTRIAL PARK, ECONOMIC AND TECHNOLOGICAL DEVELOPMENT AREA (TOUTUNHE DISTRICT) OF URUMQI
Shanghai Mio Chemical Co., Ltd
Contact:0086 21- 64401188-622
Address:16 Floor NO.2 Jiefang Building, No. 4855 Dushi Road, 201100 Shanghai, P.R.China
Yangzhou Siyu Chemical Co.,Ltd.
Contact:+86-514-87325867 13358126196
Address:Room 620 Exposition Pavilion，No. 98 Huaihai Road,Guangling District，Yangzhou City, Jiangsu Province
Doi:10.1016/j.ejmech.2021.113316
(2021)Doi:10.1016/j.bmcl.2008.10.011
(2008)Doi:10.1016/j.bmc.2004.11.045
(2005)Doi:10.1016/0047-2670(79)85019-4
(1979)Doi:10.1055/s-1979-28770
(1979)Doi:10.1021/ma0497106
(2004)
