Asymmetric synthesis of orsellinic acid type macrolides: The example of lasiodiplodin

DOI: 10.1016/0957-4166(90)90013-Z

Source and publish data:

Tetrahedron Asymmetry p. 187 - 198 (1990)

Update date:2022-08-04

Topics: Asymmetric synthesis Experimental terms Macrolides Lasiodiplodin

Authors:

Solladie

Rubio Rubio

Carreno Carreno

Ruano Ruano

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

Article abstract of DOI:10.1016/0957-4166(90)90013-Z

The asymmetric synthesis of both enantiomers of methyl lasiodiplodin is described. The chiral centers were created in the very last steps of the synthesis by asymmetric induction of a chiral sulfoxide group.

Full text of DOI:10.1016/0957-4166(90)90013-Z

Products guided by the article

Product name:(R)-Lasiodiplodin

Cas No:85551-56-0

R&D Labs maybe for 85551-56-0

UNION PHARMPRO CO.,LTD

Contact:18710867521(wechat)

Address:Rm10516,Galaxy Tech Building #2,No.25 Tangyan Rd,Hi-Tech Zone,Xi'an, China
Lonwin Chemical Group Limited

website:http://www.lonwinchem.com

Contact:Tel: 86-21-59858395

Address:No#966,Huaxu Road,Shanghai 201702,P.R.China
TIANJIN DONGRUXIANG MINERALS MARKETING CO.,LTD(expird)

Contact:22-58516360

Address:tianjin
RongCheng K&S Chemical Co.,Ltd

Contact:0631-7336369

Address:rongcheng ,shandong province china
Henan Techway Chemical Co.,Ltd.

website:http://www.techwaychem.com

Contact:+86-371-66380080

Address:No.27 Shunhe Road,

Relevant to this article

Recognition and catalysis in allylic alkylations.

Doi:10.1021/ol0258637
(2002)
Doi:10.1039/jr9470000914
(1947)
Doi:10.1021/ja01141a028
(1952)
Doi:10.1002/hlca.19290120112
(1929)
Doi:10.1021/ja01329a045
(1933)
Design and synthesis of alkyl 7,7-dihalo-3-methyl-5-(nitrophenyl)-2- azabicyclo[4.1.0]hept-3-ene-4-carboxylates with calcium channel antagonist activity

Doi:10.1016/j.bmc.2005.03.047
(2005)

Article Doi