A concise approach to enantiomerically pure carbocyclic ribose analogues. Synthesis of (4S,5R,6R,7R)-7-(hydroxymethyl)spiro[2.4]heptane-4,5,6-triol 7-O-(dihydrogen phosphate)

DOI: 10.1021/ja00167a039

Source and publish data:

Journal of the American Chemical Society p. 4374 - 4380 (1990)

Update date:2022-08-05

Topics:

Authors:

Gaudino Gaudino

Wilcox Wilcox

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

Article abstract of DOI:10.1021/ja00167a039

Full text of DOI:10.1021/ja00167a039

Products guided by the article

Product name:1,2-dideoxy-3-O-<(ethyloxy)carbonyl>-4,5-O-(1-methylethylidene)-6-O--7-O-(methoxymethyl)-D-allo-hept-1-ynitol

Cas No:127595-49-7

R&D Labs maybe for 127595-49-7

Xinxiang Junlong Biological Technology Co., Ltd.

website:https://junlongbio.lookchem.com/

Contact:86-13525059581

Address:Xinxiang City, Henan Province
SHENYANG COMEBOARD TECHNOLOGY CO., LTD

Contact:+86-24-25724626

Address:Room2210,Tianbao International Building,No.8-1 Weigong South Street,Tiexi District,Shenyang,China
Shanghai Potomer International Trade CO., LTD

Contact:+86-21-61397128

Address:Room 304,No.505 ,Caoyang Road.Shanghai,China
Synasia Inc

Contact:17316303296

Address:240 Amboy Ave
Shuanghe Bio-Technology Limited(expird)

Contact:+86-571-61710758,18968016640

Address:Jinqiao north road 916# Fuyang

Relevant to this article

KINETICS AND MECHANISM OF THE REACTION OF PHOTOINDUCED 9-ARYLOXY-1,10-ANTHRAQUINONES WITH ALCOHOLS

Doi:10.1007/BF00960658
(1990)
A Facile Synthesis of α-Trifluorodiazo Compounds

Doi:10.1016/S0022-1139(00)81567-5
(1990)
Optimization of the in vitro cardiac safety of hydroxamate-based histone deacetylase inhibitors

Doi:10.1021/jm200388e
(2011)
Chiral cationic [Cp′Mo(CO)₂(NCMe)]⁺ species-catalyst precursors for olefin epoxidation with H₂O ₂ and tert-butyl hydroperoxide

Doi:10.1002/ejic.201001065
(2011)
A FACILE SYNTHESIS OF CYANOGUANIDINES FROM THIOUREAS

Doi:10.1016/S0040-4039(00)70685-X
(1989)
Michael Reaction Inspired Atroposelective Construction of Axially Chiral Biaryls

Doi:10.1021/jacs.0c01963
(2020)

Article Doi