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Ferreira, Franck; Denichoux, Aurélien; Chemla, Fabrice; Bejjani, Joseph (2004). "Highly
Diastereoselective Syntheses of Propargylic Acid and Homopropargylic Systems".
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a saturated position on a molecular framework next to a propargylic group and thus two bonds from an
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34:Chemical structure of the propargyl group.
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98:) on a molecular framework next to an
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102:group. The name comes from mix of
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121:designates in the same manner
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144:, or substituted homologue.
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27:Chemical group (–CH₂C≡CH)
132:a 3-butynyl fragment,
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223:10.1055/s-2004-832816
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248:Propargyl compounds
69:group derived from
177:Propargyl chloride
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253:Functional groups
217:(12): 2051–2065.
187:Propargyl bromide
182:Propargyl alcohol
40:organic chemistry
16:(Redirected from
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48:functional group
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119:homopropargylic
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44:propargyl group
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243:Alkynyl groups
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192:Propiolic acid
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87:refers to a
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165:Vinyl group
96:-hybridized
85:propargylic
65:. It is an
18:Propargylic
237:Categories
198:References
91:position (
117:The term
89:saturated
83:The term
56:structure
54:with the
149:See also
108:argentum
52:propynyl
214:Synlett
172:Ethynyl
134:HC≡C−CH
129:moiety.
104:propene
100:alkynyl
75:HC≡C−CH
71:propyne
59:CH≡C−CH
127:alkyne
42:, the
160:Allyl
67:alkyl
50:of 2-
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38:In
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