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1-(-甲氧基苯基)四唑基取代的 1,2,3,4-四氢异喹啉的合成及其涉及的炔烃的转化。

Synthesis of 1-(-methoxyphenyl)tetrazolyl-Substituted 1,2,3,4-Tetrahydroisoquinolines and Their Transformations Involving Activated Alkynes.

机构信息

Organic Chemistry Department, Peoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St., 117198 Moscow, Russia.

Institute of Chemistry of Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet, Cau Giay, Hanoi 100000, Vietnam.

出版信息

Molecules. 2018 Nov 17;23(11):3010. doi: 10.3390/molecules23113010.

DOI:10.3390/molecules23113010
PMID:30453635
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6278526/
Abstract

1-(-Methoxyphenyl)tetrazolyl-substituted 6,7-dimethoxy(6,7-methylenedioxy)-1,2,3,4-tetrahydroisoquinolines formed tetrazolyl-substituted azocines in high yields by using activated alkynes. Unsubstituted at 6,7,8-aromatic fragment 1-tetrazolylisoquinoline interacted in several pathways forming tetrazolyl-substituted azocines, 1-tetrazolyl-1-R-vinylisoquinolines and 3-azaspiro[5.5]undeca-1,7,9-triene.

摘要

1-(-甲氧基苯基)四唑基取代的 6,7-二甲氧基(6,7-亚甲基二氧基)-1,2,3,4-四氢异喹啉,通过使用活化的炔烃,以高产率形成四唑基取代的偶氮化合物。6,7,8-芳环片段未取代的 1-四唑基异喹啉通过多种途径相互作用,形成四唑基取代的偶氮化合物、1-四唑基-1-R-乙烯基异喹啉和 3-氮杂螺[5.5]十一-1,7,9-三烯。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b4/6278526/333fc0e9f451/molecules-23-03010-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b4/6278526/cca03df35b85/molecules-23-03010-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b4/6278526/0ecdf6fb709a/molecules-23-03010-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b4/6278526/b524e75d615f/molecules-23-03010-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b4/6278526/1ff97b617039/molecules-23-03010-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b4/6278526/f7ac7a621ad6/molecules-23-03010-sch005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b4/6278526/333fc0e9f451/molecules-23-03010-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b4/6278526/cca03df35b85/molecules-23-03010-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b4/6278526/0ecdf6fb709a/molecules-23-03010-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b4/6278526/b524e75d615f/molecules-23-03010-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b4/6278526/1ff97b617039/molecules-23-03010-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b4/6278526/f7ac7a621ad6/molecules-23-03010-sch005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b4/6278526/333fc0e9f451/molecules-23-03010-g001.jpg

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