SYNTHESIS OF CARBOCYCLIC LIGNAN VARIANTS RELATED TO PODOPHYLLOTOXIN

DOI: 10.1246/cl.1988.1235

Source and publish data:

Chemistry Letters p. 1235 - 1238 (1988)

Update date:2022-08-04

Topics:

Authors:

Saito, Hitoshi

Nishimura, Yoshio

Kondo, Shinichi

Takeuchi, Tomio

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

Article abstract of DOI:10.1246/cl.1988.1235

Carbocyclic lignan variants related to podophyllotoxin were synthesized by a stereoselective BF₃-catalyzed coupling of podophyllotoxin derivative with chiral aminocyclitols.

Full text of DOI:10.1246/cl.1988.1235

Products guided by the article

Product name:1L-(1,2,4,5/3)-2,3,4-tri-O-benzyl-1-O-p-toluenesulfonyl-1,2,3,4,5-cyclohexanepentol

Cas No:118190-45-7

R&D Labs maybe for 118190-45-7

TLS PHARMACEUTICAL CO.,LTD

Contact:0833-5590788/5590338/5590055

Address:Victory in the town of Red Star Village,Mount Emei City,industrial concentration area storage processing logistics parkpark
Hefei TNJ chemical industry co.,ltd

website:https://www.tnjchem.com

Contact:+86-551-65418695

Address:B911 Xincheng Business Center, Qianshan Road, Hefei Anhui China
ANHUI CHEM-BRIGHT BIOENGINEERING CO.,LTD

Contact:86-561-4080321

Address:No.8 Lieshan Industrial Zone of Huaibei
Xi'an Kaixiang Photoelectric Technology Co., Ltd

website:http://www.kxmaterials.com/

Contact:86-29-15991651477

Address:Building 6, Biopharmaceutical Industry R&D Cluster Base, No. 16, Caotang 4th Road, Caotang Science and Technology Industrial Base, High-tech Zone, Xi'an City, Shaanxi Province, China
Nanjing Chemical Material Corp.(NCMC)

website:http://www.njchemm.com

Contact:0086-25-83172879

Address:B12 Technology and Innovation Building, Nanjing Tech University, No.5 New Model Road

Relevant to this article

Expedient total synthesis of small to medium-sized membrane proteins via fmoc chemistry

Doi:10.1021/ja500222u
(2014)
Copper-Catalyzed Three-Component Coupling Reaction of Azoles, Se Powder, and Aryl Iodides

Doi:10.1021/acs.joc.6b02388
(2017)
Stereoselective, Multicomponent Approach to Quaternary Substituted Hydroindole Scaffolds

Doi:10.1021/acs.orglett.0c01650
(2020)
A versatile access to enantiomerically pure 5-substituted 4-hydroxycyclohex-2-enones: An advanced hemisecalonic acid a model

Doi:10.1055/s-2007-983761
(2007)
Synthesis and anti-coronavirus activity of a series of 1-thia-4-azaspiro[4.5]decan-3-one derivatives

Doi:10.1002/ardp.201800330
(2019)
Fluorous enzymatic synthesis of phosphatidylinositides

Doi:10.1039/c4cc00022f
(2014)

Article Doi