Studies on the Synthesis of Olivin: Diastereoselective Synthesis of a Functionalized D-Fucose Derivative

DOI: 10.1016/S0040-4039(00)81890-0

Source and publish data:

Tetrahedron Letters p. 2227 - 2230 (1983)

Update date:2022-08-04

Topics:

Authors:

Roush, William R.

Harris, David J.

Lesur, Brigitte M.

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

Article abstract of DOI:10.1016/S0040-4039(00)81890-0

A short, highly diastereoselective synthesis of D-fucose derivative 4 by a route involving the addition of allylboronate reagent 7 to aldehyde 6 is described.

Full text of DOI:10.1016/S0040-4039(00)81890-0

Products guided by the article

Product name:(2S,3R)-2-((1S,2R)-1-Benzyloxy-3,3-bis-ethylsulfanyl-2-methoxy-propyl)-3-methyl-1,4-dioxa-spiro[4.5]decane

Cas No:120264-67-7

R&D Labs maybe for 120264-67-7

Chongqing maohuan Chemicals Co., Ltd

website:http://www.bschem.com

Contact:+86 13996103726

Address:Chongqing Nan'an District Tu Town
Shanghai Sunway Pharmaceutical Technology Co.,Ltd.

Contact:+86-21-5161 3915

Address:Shanghai YangPu
Shreeji pharma international

Contact:0091-265-2313036

Address:311, ATLANTIS HEIGHTS SARABHAI MAIN ROAD,VADIWADI ,VADODARA
SINO Industries Company Limited(expird)

Contact:86-29-85369724

Address:No.111, Jiefang Road, Xi’an, China
WENZHOU M&C FOREIGN TRADE CO.,LTD.

Contact:+86-577-88862917

Address:No.8 Liming West Road,Wenzhou,zhejiang,China

Relevant to this article

Doi:10.1039/jr9430000625
(1943)
Doi:10.1021/ja01215a030
(1946)
Doi:10.1021/ja00998a030
(1967)
Versatile reactivity of the bis(dihydrogen) complex RuH₂(H₂)₂(PCy₃)₂ toward functionalized olefins: Olefin coordination versus hydrogen transfer via the stepwise dehydrogenation of the phosphine ligand

Doi:10.1021/om950888d
(1996)
Study on surfactin, a cyclic depsipeptide. II. Synthesis of surfactin B₂ produced by Bacillus natto KMD 2311

Doi:10.1248/cpb.44.5
(1996)
A concise synthesis of the naphthoic acid component of neocarzinostatin chromophore featuring a new photocyclization reaction

Doi:10.1016/0040-4039(95)02268-6
(1996)

Article Doi