Asymmetric Construction of Spiro[thiopyranoindole-benzoisothiazole] Scaffold via a Formal [3 + 3] Spiroannulation-Reference-Cited by-同舟云学术

Asymmetric Construction of Spiro[thiopyranoindole-benzoisothiazole] Scaffold via a Formal [3 + 3] Spiroannulation

Published:2015-08-19 Issue:17 Volume:17 Page:4188-4191
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Chen Xiang¹,Zhang Jun-Qi¹,Yin Shao-Jie¹,Li Hai-Yan¹,Zhou Wei-Qun¹,Wang Xing-Wang¹

Affiliation:

1. Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, People’s Republic of China

Funder

Priority Academic Program Development of Jiangsu Higher Education Institutions

National Natural Science Foundation of China

Program for New Century Excellent Talents in University

Scientific and Technologic Infrastructure of Suzhou

Natural Science Foundation of the Jiangsu Higher Education Institutions

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b01951

Reference44 articles.

1. The importance of new companies for drug discovery: origins of a decade of new drugs

2. Ytterbium triflate-catalyzed asymmetric hetero Diels-Alder cycloaddition of a 1-thiabuta-1,3-diene with a chiral N-acryloyloxazolidinone dienophile. Diastereoface control by solvents or achiral additives

3. Diels-Alder cycloaddittion reactions of enaminothions with nitroalkenes

4. Regioselective synthesis of substituted 3,4-dihydro-2H-thiines from α,β-unsaturated oxathiolanes and styrene derivatives

5. Efficient Synthesis of Functionalized 2 H-Thiopyrans via Hetero- Diels- Alder Reactions of an Enaminothione with Electrophilic Olefins

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