STEREOCHEMISTRY OF 2-SUBSTITUTED 5,6-BENZO-1,3,2-DIOXARSEPINES

DOI: 10.1007/BF00959193

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 1627 - 1632 (1984)

Update date:2022-08-16

Topics:

Authors:

Arbuzov, B. A.

Aganov, A. V.

Klochkov, V. V.

Anonimova, I. V.

Chadaeva, N. A.

Lyumbitseva, O. G.

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

Article abstract of DOI:10.1007/BF00959193

Full text of DOI:10.1007/BF00959193

Products guided by the article

Product name:2,4,3-Benzodioxarsepin, 1,5-dihydro-3-phenyl-

Cas No:88861-60-3

R&D Labs maybe for 88861-60-3

ShangHai Ruiyi Medical Technology Co.,Ltd.

Contact:+86-21-54718086

Address:No951 Jianchuan RD，Minhang District
Shanghai Standard Biotech Co., Ltd.

Contact:+86-18502101150

Address:Room 103, Building 2nd, NO.720, Cailun Road , Pudong District, Shanghai, China
Hangzhou Haiqiang Chemical Co.,Ltd.

Contact:+86-571-86960370

Address:Add: 5/F, Around Town North Road,No. 10, Hangzhou, Zhejiang,China
Shanghai Apeptide Co., Ltd.

website:http://www.apeptides.com/en/

Contact:+86-21-60871011

Address:No. 80 Chuanshan Shuyuan Steet,Pudong,Shanghai
Zhejiang Hoshine Silicon Industry Co., Ltd.

Contact:86-573-89179966

Address:Zhapu Town, Pinghu City, Zhejiang, China

Relevant to this article

Discovery of a potent class I selective ketone histone deacetylase inhibitor with antitumor activity in vivo and optimized pharmacokinetic properties

Doi:10.1021/jm9004303
(2009)
Synthesis of optically active natural carotenoids and structurally related compounds. X. Synthesis of (3R,3'S,5'R)-capsanthin, 3S,5R,3'S,5'R)-capsorubin, (3'S,5'R)-cryptocapsin, and some related compounds. A new approach to optically active, five-membered-ring carotenoid building units by hydroboration

Doi:10.1002/hlca.19830660706
(1983)
Construction of furo[3,4-c]pyran skeleton starting from the Baylis-Hillman adducts via the ring-closing metathesis (RCM) reaction of exo-methylene tetrahydrofuran

Doi:10.1016/j.tet.2006.02.038
(2006)
Evaluation of 2-(piperidine-1-yl)-ethyl (PIP) as a protecting group for phenols: Stability to ortho-lithiation conditions and boiling concentrated hydrobromic acid, orthogonality with most common protecting group classes, and deprotection via Cope elimination or by mild Lewis acids

Doi:10.1016/j.tet.2021.132108
(2021)
X-ray diffraction, solution structure, and computational studies on derivatives of (3-sec-butyl-2,3-dihydro-1H-isoquinolin-4-ylidene)acetic acid: Compounds with activity as calpain inhibitors

Doi:10.1021/jo902091u
(2010)
Total synthesis of the cyclic tetrapeptide, HC-toxin

Doi:10.1016/S0040-4039(00)87855-7
(1983)

Article Doi