Et3B-Induced Radical Addition of R3SnH to Acetylenes and Its Application to Cyclization Reaction

DOI: 10.1021/ja00242a068

Source and publish data:

Journal of the American Chemical Society p. 2547 - 2549 (1987)

Update date:2022-08-04

Topics:

Authors:

Nozaki, Kyoko

Oshima, Koichiro

Utimoto, Kiitiro

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

Article abstract of DOI:10.1021/ja00242a068

Full text of DOI:10.1021/ja00242a068

Products guided by the article

Product name:Stannane, (1-pentyl-1-heptenyl)triphenyl-, (E)-

Cas No:114566-78-8

R&D Labs maybe for 114566-78-8

ABA Chemicals (Shanghai) Limited

Contact:021- 5115 9199-232

Address:Suite 18D, #201 Ningxia Road,
ChengduChroma-BiotechCo.,Ltd.

Contact:86-28-61993785

Address:No.70-13-21, North Section, Erhuan
FUJIAN SHANSHUI CHEMICAL CORP.LTD.

Contact:+86-151-59920036

Address:Jinqiao Gareden, jo@fj-xinyi.com
Huzhou City Linghu Xinwang Chemical Co.,Ltd.

Contact:86-572-3948695/3945236

Address:huzhou
Shanghai Standard Biotech Co., Ltd.

Contact:+86-18502101150

Address:Room 103, Building 2nd, NO.720, Cailun Road , Pudong District, Shanghai, China

Relevant to this article

Studies of benzothiophene template as potent factor IXa (FIXa) inhibitors in thrombosis

Doi:10.1021/jm901475e
(2010)
Synthesis of mesogenic phthalocyanine-C₆₀ donor-acceptor dyads designed for molecular heterojunction photovoltaic devices

Doi:10.3762/bjoc.5.49
(2009)
Microwave assisted synthesis of some 2, 4 dihydroxy 1, 8-naphthyridines and their derivatives devoid of solvent and catalyst

Doi:10.1515/HC.2009.15.1.35
(2009)
A direct and convenient synthesis of periodoarenes using molecular iodine

Doi:10.1055/s-0029-1217072
(2010)
A practical protocol for asymmetric synthesis of wieland-miescher and hajos-parrish ketones catalyzed by a simple chiral primary amine

Doi:10.1055/s-0033-1338891
(2013)
PdCl₂(HNMe₂)₂-catalyzed highly selective cross [2 + 2 + 2] cyclization of alkynoates and alkenes under molecular oxygen

Doi:10.1021/jo902636g
(2010)

Article Doi