The 2-(2-Chloroacetoxyethyl)benzoyl Group - Stable to Hydrogenolysis and Cleavable beside other Acyl Groups

DOI: 10.1016/0040-4039(95)01171-D

Source and publish data:

Tetrahedron Letters p. 5727 - 5730 (1995)

Update date:2022-09-26

Topics:

Authors:

Ziegler, Thomas

Pantkowski, Guido

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

Article abstract of DOI:10.1016/0040-4039(95)01171-D

The 2-(2-chloroacetoxyethyl)benzoyl (CAEB) group is prepared from isochromane in 4 steps and used as a temporary protecting group for carbohydrates.The CAEB group functions as a neighboring active, 1,2-trans-directing blocking group for glycosyl donors.It

Full text of DOI:10.1016/0040-4039(95)01171-D

Products guided by the article

Product name:Chloro-acetic acid 2-(2-chlorocarbonyl-phenyl)-ethyl ester

Cas No:171079-94-0

R&D Labs maybe for 171079-94-0

Chengdu Biopurify Phytochemicals Ltd.

website:http://www.phytopurify.com

Contact:+86-28-82633397

Address:2F,No.11 Building,No.388 Rongtaidadao CNSTP,Wenjiang Zone,Chengdu,Sichuan, China
Hubei Vanz Pharm Co.,Ltd

website:http://www.vanzpharm.com/en/index.html

Contact:86-27-84492310

Address:FANHU INDUSTRY PARK
Changzhou Welton Chemical Co., Ltd,

Contact:0086-519-85910828,85920537,85912897

Address:No.8 Jinlong Road, Binjiang Park, Changzhou, Jiangsu, China.
LIANYUNGANG YC FINE CHEMICAL CO., LTD

Contact:+86-518-858 99188

Address:Shangdong Modern Bldg, South Greenpark Road, Lianyungang, Jiangsu Pro. China
Anhui Biochem United Pharmaceutical Co., Ltd.

Contact:0086 551 5167062 / 5228268

Address:No. 30 Hongfeng Road, Hi-Tech Development Zone, Hefei (230088), China

Relevant to this article

Doi:10.1039/jr9640000130
(1964)
Vinylaluminum addition to sulfinimines (N-sulfinyl imines). Asymmetric synthesis of anti-α-alkyl β-amino esters

Doi:10.1021/jo9001504
(2009)
Chiral Synthesis via Organoboranes. 42. Selective Reductions. 57. Efficient Kinetic Resolution of Representative α-Tertiary Ketones with B-Chlorodiisopinocampheylborane

Doi:10.1021/jo951206z
(1996)
Synthesis and biological evaluation of N-[4-(2-trans-[([2,6-diamino-4(3H)-oxopyrimidin-5-yl]methyl)thio]cyclo butyl)benzoyl]-L-glutamic acid a novel 5-thiepyrimidinone inhibitor of dihydrofolate reductase

Doi:10.1002/jhet.5570320514
(1995)
Role of conformation and electronic structure in the chemistry of ground and excited state o-pyrazolylphenylnitrenes

Doi:10.1021/ja043988w
(2005)
Diastereoselective reduction of hemiacetals derived from 2,3-o-isopropylidene derivatives of carbohydrate lactones

Doi:10.1246/cl.1996.67
(1996)

Article Doi

The 2-(2-Chloroacetoxyethyl)benzoyl Group - Stable to Hydrogenolysis and Cleavable beside other Acyl Groups

DOI: 10.1016/0040-4039(95)01171-D

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0040-4039(95)01171-D

Full text of DOI:10.1016/0040-4039(95)01171-D

Products guided by the article

R&D Labs maybe for 171079-94-0

Relevant to this article

Vinylaluminum addition to sulfinimines (N-sulfinyl imines). Asymmetric synthesis of anti-α-alkyl β-amino esters

Chiral Synthesis via Organoboranes. 42. Selective Reductions. 57. Efficient Kinetic Resolution of Representative α-Tertiary Ketones with B-Chlorodiisopinocampheylborane

Synthesis and biological evaluation of N-[4-(2-trans-[([2,6-diamino-4(3H)-oxopyrimidin-5-yl]methyl)thio]cyclo butyl)benzoyl]-L-glutamic acid a novel 5-thiepyrimidinone inhibitor of dihydrofolate reductase

Role of conformation and electronic structure in the chemistry of ground and excited state o-pyrazolylphenylnitrenes

Diastereoselective reduction of hemiacetals derived from 2,3-o-isopropylidene derivatives of carbohydrate lactones