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

Nanjing Vincero International Trading Co.,Ltd

Contact:8618936897229

Address:NO.68, ZhuShan Road, JiangNing WanDa Plaza, Building E Room 1703
Liaoning Yufeng Chemical Co.,Ltd.

Contact:86-0419-3418888

Address:The metallurgical industrial zone,shoushan town, Liaoyang, Liaoning, China
MedicalChem(Yancheng)Manuf.Co.,Ltd.

Contact:+86-515-84383366

Address:Touzeng BinHai, YanCheng City, JiangSu Province, 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
Hangzhou Deli Chemical Co.,Ltd.

website:http://www.dlchemical.com

Contact:86 571 28006267

Address:Tangxi Industrial Area, Yuhang District, Hangzhou

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