Scholarly article on (+/-)-cis-flavan-4-ol acetate 27439-11-8 from Journal of the American Chemical Society p. 700,705

DOI: 10.1021/ja01208a052

Source and publish data:

Journal of the American Chemical Society p. 700,705 (1946)

Update date:2022-08-05

Topics:

Authors:

Geissman

Clinton Clinton

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

Article abstract of DOI:10.1021/ja01208a052

Full text of DOI:10.1021/ja01208a052

Products guided by the article

Product name:(+/-)-cis-flavan-4-ol acetate

Cas No:27439-11-8

R&D Labs maybe for 27439-11-8

Merit Special New Material Co., Ltd.

website:http://www.ycmerit.com

Contact:13585104388

Address:No.15 Xiexin Road,Funing Economic Development Zone,JiangSu,P.R.China
MINS GROUP CO.,LIMITED

Contact:18669908765

Address:Zibo City, Shandong Province, P.R.China
QINGDAO TAOSIGN INTERNATIONAL TRADE CO.,LIMITED

Contact:+86-0532-82683616

Address:RM1402, Doublestar Seacoase 7#, No. 5 Guizhou Road, Qingdao, Shandong, China
Beijing Huikang Boyuan Chemical Tech Co.,LTD

Contact:+86-10-68862197

Address:No.7 Haiying Road,Science City,Fengtai District,Beijing,China
Shanghai Yuanding Chem. Sci. & Tech. Co., Ltd.

website:http://www.shydtec.com

Contact:86-21-57721279

Address:Science and Technology Park, Songjiang District, Shanghai, China

Relevant to this article

Enantioselective formal total synthesis of roseophilin.

Doi:10.1021/ol005750s
(2000)
Aerobic Co-/ N-Hydroxysuccinimide-Catalyzed Oxidation of p-Tolylsiloxanes to p-Carboxyphenylsiloxanes: Synthesis of Functionalized Siloxanes as Promising Building Blocks for Siloxane-Based Materials

Doi:10.1021/jacs.8b12600
(2019)
Reactions of [(μ-RS)(μ-S){Fe₂(CO)₆}₂(μ ₄-S)]^- with acid chlorides and diacid chlorides. Crystal structure of (μ-PhCH₂S)[μ-CH₂=C(Me)COS][Fe₂(CO) ₆]₂

Doi:10.1016/S0022-328X(00)00042-5
(2000)

Rh-Catalyzed, Regioselective, C-H Bond Functionalization: Access to Quinoline-Branched Amines and Dimers

Doi:10.1021/acs.orglett.6b02848
(2016)
Total synthesis of ( - )-cylindrocyclophanes A and F exploiting the reversible nature of the olefin cross metathesis reaction

Doi:10.1021/ja0106164
(2001)
Doi:10.1016/S0040-4039(01)97826-8
(1970)

Article Doi

DOI: 10.1021/ja01208a052

Source and publish data: