1,6-Stannatropic Strategy: Effective Generation and Cyclization of 1,5-Dipoles from o-Stannylmethylated Thioanilides or Phenyl Isothiocyanates-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

1,6-Stannatropic Strategy: Effective Generation and Cyclization of 1,5-Dipoles from o-Stannylmethylated Thioanilides or Phenyl Isothiocyanates

Published:2006-07-21 Issue:17 Volume:8 Page:3693-3695
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Minakata Satoshi¹,Kasano Yukihiro¹,Ota Hirofumi¹,Oderaotoshi Yoji¹,Komatsu Mitsuo¹

Affiliation:

1. Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Yamadaoka 2-1, Suita, Osaka 565-0871, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0612758

Reference34 articles.

1. 1,5-Dipolar cyclizations

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. 2-(Hetero)Arylindoles;Privileged Structures in Drug Discovery;2018-03-09

2. Base-promoted domino reaction for the synthesis of 2,3-disubstituted indoles from 2-aminobenzaldehyde/2-amino aryl ketones, tosylhydrazine, and aromatic aldehydes;Tetrahedron;2016-08

3. Other Tin-Mediated Indole Syntheses;Indole Ring Synthesis;2016-06-17

4. Intramolecular addition of diarylmethanols to imines promoted by KOt-Bu/DMF: a new synthetic approach to indole derivatives;Organic & Biomolecular Chemistry;2016

5. Furan Ring-Opening/Indole Ring-Closure: Pictet-Spengler-Like Reaction of 2-(o-Aminophenyl)furans with Aldehydes;European Journal of Organic Chemistry;2010-02

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP