Journal of Organic Chemistry p. 2135 - 2139 (1991)
Update date:2022-08-04
Topics:
Casiraghi, Giovanni
Colombo, Lino
Rassu, Gloria
Spanu, Pietro
Enantiomerically pure undecose acetonide 9 was synthesized, through heptose intermediate 5, starting with D-glyceraldehyde acetonide (1).The key steps were two consecutive four-carbon homologations, each consisting of four reactions: (i) stereoselective elongation of the aldehyde precursor with 2-(trimethylsiloxy)furan, giving Cn+4 butenolide templates 2 and 6, (ii) anti-selective cis-dihydroxylation of the butenolide double bond, giving fully functionalized lactones 3 and 7, (iii) lactone ring opening and protection, giving open-chain methyl esters 4 and 8, and (iv) DIBAL reduction to aldoses 5 and 9.At the end of the eight-step sequence, undecose 9 was prepared in a 5.1percent overall yield, which corresponded to a 69.5percent average yield per step.
View MoreLianYunGang Chiral Chemical(CHINA) CO.,LTD
Contact:+86-518-83616958 +86-519-82884848
Address:LianYunGang Chemical Industry Park (JiangSu)
Sichuan WeiKeqi Biological Technology Co., Ltd.
Contact:86-028-81700200
Address:sichuan Chengdu Qingjiang Zhonglu 63号
Wuhan Soleado Technology Co.,Ltd.
Contact:86-2783341481 18971291927
Address:RM2405 Unit 1 Builing 1, Taiyin Tower, Changqing Road,Wuhan China
Contact:+86-570-4336358
Address:No.87 Building,Tianqian,Sidu Town
Contact:86-510-82853889
Address:Rm.3732, No.18-2,Yonghe Rd.,Wuxi,Jiangsu,214023,China
Doi:10.1016/j.bmcl.2011.04.076
(2011)Doi:10.1021/jo00006a015
(1991)Doi:10.1002/chem.201101048
(2011)Doi:10.1055/s-0030-1260776
(2011)Doi:10.1021/jo00005a008
(1991)Doi:10.1002/chem.201503621
(2015)