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

Shanghai Massive Chemical Technology Co., Ltd.

website:http://www.massivechem.com/

Contact:+86 21 34943721

Address:Room 435, 4th floor, Building 9, No. 2568 Gudai Road,Minhang District, Shanghai,
Synchemie Co., Ltd.

website:http://www.synchemie.com/

Contact:+86-574-87642758

Address:Room 901, Yinyi Bund Building， 132 Renmin Road
Hunan Warrant Chiral Pharmaceutical Co., Ltd.

website:http://www.hwcpharm.com

Contact:+86-0731-85910593

Address:LuTian Road No.28
Wuhan Jing Chu Chen Pharmaceutical Chemical Co., Ltd.

Contact:027-88877050

Address:Wuhan
Changzhou Yongxu Chemical Co.,Ltd

Contact:86-0519-85286591

Address:Room 1812,Wanda Plaza B,Xinbei District,Changzhou,Jiangsu,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