ChemInform Abstract: A Catalytic Approach for the Synthesis of Allylic Azides from Aryl Vinyl Carbinols.

G. Srinu; P. Srihari

doi:10.1002/chin.201332065

ChemInform Abstract: A Catalytic Approach for the Synthesis of Allylic Azides from Aryl Vinyl Carbinols.

ChemInform ◽

10.1002/chin.201332065 ◽

2013 ◽

Vol 44 (32) ◽

pp. no-no

Author(s):

G. Srinu ◽

P. Srihari

Keyword(s):

Allylic Azides

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Steric constraints against [3,3]-sigmatropic rearrangement of allylic azides. A convenient approach to β-l-4-aminopent-2-enoglyceropyranosides

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(01)00450-5 ◽

2001 ◽

Vol 12 (19) ◽

pp. 2731-2741 ◽

Cited By ~ 15

Author(s):

Cristiana Fava ◽

Roberta Galeazzi ◽

Giovanna Mobbili ◽

Mario Orena

Keyword(s):

Sigmatropic Rearrangement ◽

Convenient Approach ◽

Allylic Azides ◽

Steric Constraints

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Organic Azides. 3. Ultrasound Synthesis of Propargyl Azide, Azidoacetonitrile and Primary Allylic Azides.

Acta Chemica Scandinavica ◽

10.3891/acta.chem.scand.38b-0895 ◽

1984 ◽

Vol 38b ◽

pp. 895-898 ◽

Cited By ~ 25

Author(s):

Hanno Priebe ◽

Gunner Borch ◽

Synnøve Liaaen-Jensen ◽

Anders Måhlén ◽

Lars Mörch

Keyword(s):

Organic Azides ◽

Allylic Azides

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Practical regio- and stereoselective azidation and amination of terminal alkenes

Organic & Biomolecular Chemistry ◽

10.1039/c8ob02734j ◽

2018 ◽

Vol 16 (48) ◽

pp. 9354-9358 ◽

Cited By ~ 5

Author(s):

Olatunji S. Ojo ◽

Octavio Miranda ◽

Kyle C. Baumgardner ◽

Alejandro Bugarin

Keyword(s):

Allylic Amines ◽

Reaction Conditions ◽

Metal Free ◽

Terminal Alkenes ◽

Allylic Azides

A metal-free synthesis of allylic azides and allylic amines was achieved under mild reaction conditions, which represents a milder alternative for azidation and amination reactions.

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Perfluoroalkyl-Induced Dimerization of Allylic Azides

Synthesis ◽

10.1055/s-1978-24869 ◽

1978 ◽

Vol 1978 (09) ◽

pp. 705-706 ◽

Cited By ~ 7

Author(s):

Elfriede MANHART ◽

Konrad von WERNER

Keyword(s):

Allylic Azides

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A catalytic approach for the synthesis of allylic azides from aryl vinyl carbinols

Tetrahedron Letters ◽

10.1016/j.tetlet.2013.02.094 ◽

2013 ◽

Vol 54 (19) ◽

pp. 2382-2385 ◽

Cited By ~ 12

Author(s):

G. Srinu ◽

P. Srihari

Keyword(s):

Allylic Azides

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Claisen rearrangements of equilibrating allylic azides

Organic & Biomolecular Chemistry ◽

10.1039/c1ob05972f ◽

2011 ◽

Vol 9 (20) ◽

pp. 7057 ◽

Cited By ~ 21

Author(s):

Donald Craig ◽

John W. Harvey ◽

Alexander G. O'Brien ◽

Andrew J. P. White

Keyword(s):

Claisen Rearrangements ◽

Allylic Azides

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ChemInform Abstract: On the Flexibility of Allylic Azides as Synthetic Intermediates.

ChemInform ◽

10.1002/chin.199612241 ◽

2010 ◽

Vol 27 (12) ◽

pp. no-no

Author(s):

B. M. TROST ◽

S. R. PULLEY

Keyword(s):

Synthetic Intermediates ◽

Allylic Azides

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ChemInform Abstract: REACTION OF HYDRAZOIC ACID/BORON TRIFLUORIDE ETHERATE ON STEROIDAL ALLYLIC ALCOHOLS. STEREOCONTROLLED SYNTHESIS OF ALLYLIC AZIDES AND AMINES

Chemischer Informationsdienst ◽

10.1002/chin.197901311 ◽

1979 ◽

Vol 10 (1) ◽

Author(s):

I. Z. KABORE ◽

KHUONG-HUU-QUI KHUONG-HUU-QUI ◽

A. PANCRAZI

Keyword(s):

Boron Trifluoride ◽

Boron Trifluoride Etherate ◽

Allylic Alcohols ◽

Hydrazoic Acid ◽

Stereocontrolled Synthesis ◽

Allylic Azides

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ChemInform Abstract: Efficient Synthesis of Allylic Azides and One-Pot Regioselective Synthesis of 1,4-Disubstituted 1,2,3-Triazoles from Homoallyl Alcohols.

ChemInform ◽

10.1002/chin.201047126 ◽

2010 ◽

Vol 41 (47) ◽

pp. no-no

Author(s):

P. Surendra Reddy ◽

V. Ravi ◽

B. Sreedhar

Keyword(s):

Regioselective Synthesis ◽

Efficient Synthesis ◽

One Pot ◽

Allylic Azides

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Highly selective hydrosilylation of equilibrating allylic azides

Chemical Communications ◽

10.1039/d0cc01316a ◽

2020 ◽

Vol 56 (37) ◽

pp. 5038-5041

Author(s):

Ruzhang Liu ◽

Zhen Wei ◽

Juan Wang ◽

Yongmei Liu ◽

Huaiguo Xue

Keyword(s):

Functional Group ◽

Allylic Azides ◽

Pt Catalyzed

Pt-catalyzed hydrosilylation of equilibrating allylic azides provides 3-azidopropansilanes with high chemoselectivity, regioselectivity, and excellent functional group tolerance.

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