Total synthesis of (+)-duocarmycin SA

DOI: 10.1021/ja00051a045

Source and publish data:

Journal of the American Chemical Society p. 10056 - 10058 (1992)

Update date:2022-08-04

Topics:

Authors:

Boger Boger

Machiya Machiya

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

Article abstract of DOI:10.1021/ja00051a045

Full text of DOI:10.1021/ja00051a045

Products guided by the article

Product name:duocarmycin

Cas No:144667-38-9

R&D Labs maybe for 144667-38-9

zhenjiang runjing high purity chemical co ltd

Contact:+86-511-83361155

Address:No.8.haixi road,international chemical park
Jiangsu Jiuri Chemical Co.,Ltd.

Contact:+86-519-82118868

Address:Tianwang Town, Jurong City, Jiangsu Province, China
Hisyntech Corporation Limited

Contact:0086-22-23410962

Address:17-201, Ningfuli, Shuishanggongyuandong road,Nankai district, Tianjin, China
Shanghai Kangxin Chemical Co., Ltd

Contact:+86 21 60717227

Address:118,Ganbai Village,Waigang Town,Jiading District,Shanghai
Shuanghe Bio-Technology Limited(expird)

Contact:+86-571-61710758,18968016640

Address:Jinqiao north road 916# Fuyang

Relevant to this article

Reaction of ethyl 3,3-diaminoacrylate with pyrimidine series o-chloro ketones. Synthesis of pyrido[4,3-d]pyrimidines and 6H-1,3,6,7-tetra- azaphenalenes

Doi:10.1007/s10593-013-1269-2
()
A new zinc(II) coordination polymer based on 5-methylisophthalic acid and 4,4′-dipyridylsulfide: Synthesis, structure, and photoluminescent properties

Doi:10.1080/15533174.2012.740752
(2013)
Activated dopamine derivatives as primers for adhesive-patch fixation of bone fractures

Doi:10.1039/c5ra23142f
(2016)
Direct Conversion of N-Alkylamines to N-Propargylamines through C-H Activation Promoted by Lewis Acid/Organocopper Catalysis: Application to Late-Stage Functionalization of Bioactive Molecules

Doi:10.1021/jacs.0c08599
(2020)
Scandium triflate-catalyzed D-fructofuranosylation reactions using disaccharide units

Doi:10.3987/COM-12-S(N)66
(2012)
Synthesis of multivalent carbohydrate-centered glycoclusters as nanomolar ligands of the bacterial lectin LecA from pseudomonas aeruginosa

Doi:10.1002/chem.201300135
(2013)

Article Doi