Stereocontrolled synthesis of all stereoisomers of the proposed flavolipin

DOI: 10.1016/0040-4039(96)00705-8

Source and publish data:

Tetrahedron Letters p. 3875 - 3876 (1996)

Update date:2022-08-03

Topics:

Authors:

Shiozaki, Masao

Deguchi, Noriko

Mochizuki, Takashi

Nishijima, Masahiro

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

Article abstract of DOI:10.1016/0040-4039(96)00705-8

All four stereoisomers of flavolipin were synthesized from D-glucose in a stereocontrolled manner. None of them was identical with the reported natural product.

Full text of DOI:10.1016/0040-4039(96)00705-8

Products guided by the article

Product name:(R)-3-Hydroxy-15-methyl-hexadecanoic acid benzhydryl ester

Cas No:179869-81-9

R&D Labs maybe for 179869-81-9

Changzhou Sunsheng Chem Co., Ltd

Contact:+1-(989)-854-0648

Address:No. 28 Yinshan Rd., Xixiashu Industrial Park
Shanghai Yingrui Biopharma Co., Ltd

Contact:021-3358 8661*8003

Address:shanghai
shanghai jiuling chemical co.,ltd.

Contact:+86-21-50387295

Address:Zaozhuang Road, Pudong, Shanghai City. China
Ring Specialty Chemicals Inc.

Contact:+1-416-493-6870

Address:Toronto, Canada
Guangzhou Trojan Pharmatech Ltd

website:https://www.trojanpharm.com

Contact:86-020-82350801

Address:Room 501, Building G11, South China Advanced Materials Innovation Park, 31 Kefeng Road, Science City, Guangzhou, China 510663

Relevant to this article

Synthesis of η-arene derivatives of chromium and molybdenum containing Lewis-acid boron substituents

Doi:10.1039/DT9960002467
(1996)
Nucleosides and nucleotides. 152. 1-(3-C-ethynyl-β-D-ribo-pentofuranosyl)uracil as a broad spectrum antitumor nucleoside

Doi:10.1016/0960-894X(96)00339-3
(1996)
Selective mono-dealkylation of tetra-p-tert-butyl-calix[4]arene at the upper rim

Doi:10.1080/00397919608004615
(1996)
Synthesis and structure-activity relationship studies in translocator protein ligands based on a pyrazolo[3,4-b]quinoline scaffold

Doi:10.1021/jm200770f
(2011)
An Improved Protocol for the Synthesis and Purification of Yariv Reagents

Doi:10.1021/acs.joc.0c01812
(2020)
Novel transient receptor potential vanilloid 1 receptor antagonists for the treatment of pain; Structure-activity relationships for ureas with quinoline, isoquinoline, quinazoline, phthalazine, quinoxaliue, and cinnoline moieties

Doi:10.1021/jm0492958
(2005)

Article Doi