Milbemycin synthesis: Synthesis of 6β-hydroxy-3,4-dihydromilbemycin E

DOI: 10.1016/S0040-4039(00)79699-7

Source and publish data:

Tetrahedron Letters p. 2269 - 2272 (1991)

Update date:2022-07-29

Topics:

Authors:

Karim, Sufia

Parmee, Emma R.

Thomas, Eric J.

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

Article abstract of DOI:10.1016/S0040-4039(00)79699-7

The hydroxycyclohexanone (7) is readily available via a Robinson annelation, and is converted into the hydroxybutenolide (15) which is incorporated into a synthesis of 6β-hydroxy-3,4-dihydromilbemycin E (28).

Full text of DOI:10.1016/S0040-4039(00)79699-7

Products guided by the article

Product name:6β-Hydroxy-3,4-dihydromilbemycin E

Cas No:135415-62-2

R&D Labs maybe for 135415-62-2

Henan Surface Industry Co Ltd

Contact:86-371-86169316

Address:No.1,Shakou Road,Zhengzhou,China
Shandong LuZhou Amino Acid Co., Ltd

Contact:86-539-2218025

Address:yishui economic and technical development zone zhenxing south road
Shanghai Dianyang Industry Co.,ltd

Contact:+86 21 6492 4669

Address:Chejing RD, Songjiang District, Shanghai, China
Kaymossy BioChem Tech Co., Ltd

website:http://www.kaimosi.com

Contact:0571-87191913/0571-87199097

Address:Room 215, Building 3rd, No.288 Ningxia Road, Qingdao city, China
Hunan Haili Chemical Industry Co.,Ltd.

Contact:+86-731-85521860

Address:No.251, 2nd Section, Furong Road, Changsha,Hunan,China

Relevant to this article

Clickosomes - Using triazole-linked phospholipid connectors to fuse vesicles

Doi:10.1039/c2cc16827h
(2012)
Synthesis and antifungal evaluation of pyrido[1,2-a]indole-1,4-diones and benzo[f]pyrido[1,2-a]indole-6,11-diones

Doi:10.1016/j.bmcl.2011.10.092
(2012)
Using oppositely charged ions to operate a three-station [2]rotaxane in two different switching modes

Doi:10.1021/ol203401d
(2012)
New tetraphenylethene-based efficient blue luminophors: Aggregation induced emission and partially controllable emitting color

Doi:10.1039/c1jm14054j
(2012)
Copper-catalyzed [5 + 1] annulation of 2-ethynylanilines with an N, O -acetal leading to construction of quinoline derivatives

Doi:10.1021/ol203360g
(2012)
Syntheses and 1H NMR Conformational Analyses of Diastereomeric 4,4'-(4,5-Dihydroxy-1,2-cyclohexanediyl)bis(2,6-piperazinedione)s and a Synthetically Related Tricyclic Octahydro-2,2-dimethyl-6-oxo-1,3-dioxolo<4,5-g>quinoxaline-5,8-diacetic Acid Ester

Doi:10.1021/jo00018a039
(1991)

Article Doi