Annulation of heterocyclic rings on aromatic templates: The quinone monoketal route

DOI: 10.1016/0040-4039(96)00424-8

Source and publish data:

Tetrahedron Letters p. 2881 - 2884 (1996)

Update date:2022-08-03

Topics:

Authors:

Ciufolini, Marco A.

Dong, Qing

Yates, Matthew H.

Schunk, Stefan

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

Article abstract of DOI:10.1016/0040-4039(96)00424-8

A double conjugate addition sequence anneals heterocyclic rings onto a 2-alkyl quinone monoketal intermediate. This operation, reminiscent of a Barco annulation, proceeds in excellent overall yield. The new chemistry offers interesting opportunities in al

Full text of DOI:10.1016/0040-4039(96)00424-8

Products guided by the article

Product name:2-tert-Butyl-5-((Z)-4-hydroxy-but-2-enylamino)-4,4-dimethoxy-cyclohex-2-enone

Cas No:177995-29-8

R&D Labs maybe for 177995-29-8

Xinchang Jiu Xin Pharmaceutical Co., Ltd

website:http://www.jiuxinpharm.com

Contact:86 137 5756 8585

Address:Poyang industry Park
Shanghai Yingrui Biopharma Co., Ltd

Contact:021-3358 8661*8003

Address:shanghai
JenKem Technology Co., Ltd.

Contact:86-10-62983737; +86-10-51287608

Address:4/F Building C, 2 Shangdi Xinxi Road
Shanghai Apeptide Co., Ltd.

website:http://www.apeptides.com/en/

Contact:+86-21-60871011

Address:No. 80 Chuanshan Shuyuan Steet,Pudong,Shanghai
Hisyntech Corporation Limited

Contact:0086-22-23410962

Address:17-201, Ningfuli, Shuishanggongyuandong road,Nankai district, Tianjin, China

Relevant to this article

Ruthenium(II) Charge-Transfer Sensitizers Containing 4,4′-Dicarboxy-2,2′-bipyridine. Synthesis, Properties, and Bonding Mode of Coordinated Thio- and Selenocyanates

Doi:10.1021/ic9515665
(1996)
α N-O turn induced by fluorinated α-aminoxy diamide: synthesis and conformational studies

Doi:10.1016/j.tet.2009.09.113
(2009)
Structure-activity relationships of benzimidazoles and related heterocycles as topoisomerase I poisons

Doi:10.1016/0968-0896(96)00047-8
(1996)
Novel carbon-carbon bond formation through Mizoroki-Heck type reaction of silanols and organotin compounds

Doi:10.1246/bcsj.73.1409
(2000)
Synthesis and structure-activity relationships of aroylpyrrole alkylamide bradykinin (B₂) antagonists

Doi:10.1016/S0960-894X(03)00104-5
(2003)
The preparation and structure of ammonia and alkylamine addition compounds of phosphine diborane, B₂H₆·PH₃·NR₃

Doi:10.1021/ic50056a001
(1967)

Article Doi