Synthesis of the C17-C27 fragment of bryostatin 3

DOI: 10.1016/S0040-4039(98)01577-9

Source and publish data:

Tetrahedron Letters p. 7349 - 7352 (1998)

Update date:2022-08-04

Topics:

Authors:

Obitsu, Tetsuo

Ohmori, Ken

Ogawa, Yasuyuki

Hosomi, Hiroyuki

Ohba, Shigeru

Nishiyama, Shigeru

Yamamura, Shosuke

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

Article abstract of DOI:10.1016/S0040-4039(98)01577-9

The key synthetic intermediate corresponding to the C17 - C27 positions of bryostatin 3, has successfully been synthesized. The newly constructed stereogenic centers were unambiguously confirmed by X-ray crystallographic analysis.

Full text of DOI:10.1016/S0040-4039(98)01577-9

Products guided by the article

Product name:(3S,5S,6R)-2-(2-Benzenesulfonyl-1,1-dimethyl-ethyl)-3,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-[2-(tert-butyl-diphenyl-silanyloxy)-eth-(E)-ylidene]-6-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-ylmethyl)-tetrahydro-pyran-2-ol

Cas No:214827-31-3

R&D Labs maybe for 214827-31-3

Shenyang Mole pharmaceutical Technology Development Co.,Ltd

Contact:+86-24-31204918/13889278616

Address:No.44, wanliutang road, shenhe District of Shenyang
Sinonine Industry Co.,Ltd

Contact:86+21-56421993

Address:3F,BUILDING 10,NO.2889 JINKE ROAD, SHANGHAI.
Wuhan Biet Co., Ltd

website:http://www.biet.com.cn/

Contact:+86-27-8369 8488

Address:No. 6, Building 21, China Merchants Fanwang, Sixin North Road, Hanyang District, Wuhan City, Hubei Province
Xiamen Kaijia Imp & Exp Co., Ltd.

Contact:86-592-5101177

Address:Room406 Luhui Building No. 65 Haitian Road Huli Xiamen,China.
Luyunjia Chemistry Xiamen Limited

Contact:86-592-5360779

Address: Huli District, Xiamen, China

Relevant to this article

Doi:10.1039/DT9790002015
()
Ring reversal of a spirocyclic patchouli odorant: Molecular modeling, synthesis, and odor of 6-hydroxy-1,1,6-trimethylspiro[4.5]decan-7-one

Doi:10.1002/ejoc.200600815
(2007)
New methods and reagents in organic synthesis. 17. Trimethylsilyldiazomethane (TMSCHN₂) as a stable and safe substitute for hazardous diazomethane. Its application to the Arndt-Eistert synthesis

Doi:10.1248/cpb.29.3249
(1981)
One-Pot Synthesis of Diazirines and ¹⁵N₂-Diazirines from Ketones, Aldehydes and Derivatives: Development and Mechanistic Insight

Doi:10.1002/adsc.202100679
(2021)
Highly enantioselective l-thiaproline catalyzed α-aminoxylation of aldehydes in aqueous media

Doi:10.1039/b817950f
(2009)
Synthesis and antibacterial activity of some aryloxy/thioaryloxy oxazolidinone derivatives

Doi:10.1016/j.bmcl.2004.06.096
(2004)

Article Doi