Studies on transfer ribonucleic acids and related compounds. XXXIV. Stepwise diester or partial triester synthesis of penta- to octanucleotides corresponding to residues 41--46, 47--54, 61--65 and 66--71 of tRNAfMet of E. coli.

DOI: 10.1248/cpb.28.2450

Source and publish data:

Chemical and pharmaceutical bulletin p. 2450 - 2459 (1980)

Update date:2022-08-05

Topics: Synthesis coli Residues

Authors:

Ohtsuka Ohtsuka

Miyake Miyake

Markham Markham

Nakagawa

Ikehara Ikehara

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

Article abstract of DOI:10.1248/cpb.28.2450

Full text of DOI:10.1248/cpb.28.2450

NII-Electronic Library Service

Products guided by the article

Product name:bzC(Bz)p(CE)ibG(Bz)pibG(Bz)2

Cas No:65798-67-6

R&D Labs maybe for 65798-67-6

Tai zhou world Pharm & Chem Co., Ltd

Contact:+86-576-85301198

Address:Rome 1001,wangjiang plaza,unti 2,jinshan east Road linhai,zhejiang,china
guide(suzhou) fine materials co. ltd

Contact:0512-80972173

Address:21st Building, No.369 Lushan Rd, New District Suzhou China 215129
SHENZHEN PENGCHENG REDSTAR INDUSTRY CO.,LTD

Contact:+86-755-82412922

Address:Room 8066, East Block, Square City, Jiabin Road, Luohu District
Hubei anhuang chemical Co.Ltd

Contact:

Address:308# dongwu avenue dongxihu district wuhan city
Chongqing maohuan Chemicals Co., Ltd

website:http://www.bschem.com

Contact:+86 13996103726

Address:Chongqing Nan'an District Tu Town

Relevant to this article

Doi:10.1002/apmc.1978.050660108
(1978)
Novel broad spectrum virucidal molecules against enveloped viruses

Doi:10.1371/journal.pone.0208333
(2018)
Synthesis and local anesthetic activity of benzo[b]furan derivatives.

Doi:10.1002/jps.2600670136
(1978)
Alkyl and aryl complexes of platinum(II) and palladium(II) containing the tri(1-cyclohepta-2,4,6-trienyl)phosphane ligand. Intramolecular dynamics and signs of coupling constants

Doi:10.1016/S0020-1693(03)00129-4
(2003)
Synthesis of cimetidine

Doi:10.1002/ardp.19833160807
(1983)
Conjugation of poor inhibitors with surface binding groups: A strategy to improve inhibition

Doi:10.1039/b305179j
(2003)

Article Doi