Regioselective deprotection of p-methoxybenzyl ethers of furanose derivatives

DOI: 10.1016/S0040-4039(99)00396-2

Source and publish data:

Tetrahedron Letters p. 2883 - 2886 (1999)

Update date:2022-09-26

Topics:

Authors:

Bouzide, Abderrahim

Sauve, Gilles

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

Article abstract of DOI:10.1016/S0040-4039(99)00396-2

Reaction of per-p-methoxybenzylated hexofuranoses and pentofuranoses with either a catalytic amount of tin chloride dihydrate (SnCl₂·2H₂O) or 0.5-10% solution of trifluoroaoetic acid in dichloromethane afforded regioselectively the corresponding monosaccharide derivatives having a single free hydroxyl group at C(5) in good yields.

Full text of DOI:10.1016/S0040-4039(99)00396-2

Products guided by the article

Product name:(3aR,5R,6S,6aR)-5-[(R)-2-Benzyloxy-1-(4-methoxy-benzyloxy)-ethyl]-6-(4-methoxy-benzyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole

Cas No:222845-24-1

R&D Labs maybe for 222845-24-1

BrightGene Bio-Medical Technology Co., Ltd.

website:https://en.bright-gene.com/

Contact:+86-512-62551801

Address:Building C25 - C31, No. 218 Xinghu Road, Suzhou Industrial Park, Suzhou, Jiangsu, China.
Hubei Xinghuo Chemical Co., Ltd.,

Contact:13925817279 13907299441

Address:Xinghuo Fine Chemistry Industrial Park, Xiaochang County, Hubei Province, China
Shanghai doly chemical Co.,Ltd

Contact:+86-21-34716221

Address:No.328,WuHe Roard,MinHang,ShangHai China
Jiaxing Trustworthy Import And Export Co.,Ltd

Contact:+86-573-82030555

Address:Room 1202, Unit B, Charming plaza,No.1558 East Zhongshan Road , Jiaxing City, Zhejiang Province, China.
Nanjing Chemical Material Corp.(NCMC)

website:http://www.njchemm.com

Contact:0086-25-83172879

Address:B12 Technology and Innovation Building, Nanjing Tech University, No.5 New Model Road

Relevant to this article

Stereochemical determination of the unique acrylate moiety at the 17-position in chlorophylls-c from a diatom Chaetoseros calcitrans and its effect upon electronic absorption properties

Doi:10.1039/b900802k
(2009)
Regioselective alkylation and arylation at the 6-position of pyrimidine: Synthesis of 5-alkyl-6-arylmethyl-2,4-pyrimidinediones

Doi:10.1080/00397919908086130
(1999)
Doi:10.1039/jr9650006141
(1965)
The first total synthesis of the core class II diasialylated hexasaccharide as a building block for glycopeptide synthesis

Doi:10.1016/S0040-4039(99)00605-X
(1999)
Synthesis of new thiophene-substituted 3,3-diphenyl-3H-naphtho[2,1-b]pyrans by cross-coupling reactions, precursors of photomodulated materials

Doi:10.1002/ejoc.200300033
(2003)
Doi:10.1021/jo00828a047
(1970)

Article Doi