This work discusses the model that explains the aspects of photopolymerization of methyl methacrylate initiated by dye/amine systems. This model is based on a simulation that uses differential equations. A similar model following the hypothesis presented here was used with success in a preliminary work, by Magini and Rodrigues (2005), to describe the cationic photopolymerization of THF in the presence of sensitizers/sulfonium salt systems. Using the same structure was possible to generate a straight correlation between experimental and theoretical results for this system, free radically initiated, opening an important theoretical understanding about the photopolymerization systems and their chemical relations during the reaction.

Marcio Magini

Máira R. Rodrigues

Dynamical Model to Describe the Interactions between the Chemical Components in Environment of Photopolymerization of MMA by Dye/Amine Systems

A novel and efficient three-component one-pot synthesis of benzo[<svg style="vertical-align:-0.13794pt;width:7.4749999px;" id="M2" height="10.7375" version="1.1" viewBox="0 0 7.4749999 10.7375" width="7.4749999"  xmlns="http://www.w3.org/2000/svg">
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			<text transform="matrix(1,0,0,-1,-71.95,63.6)">
				<tspan style="font-size: 12.50px; " x="0" y="0">𝑏</tspan>
			</text>

		</g>
	</g>
</svg>]1,8-naphthyridines by 2-amino-4-methylquinoline, aromatic aldehydes, and malononitrile was done. The reaction was catalyzed by an acidic Bismuth(III) chloride, functionalized Bismuth(III) chloride, at room temperature to give various benzo[<svg style="vertical-align:-0.13794pt;width:7.4749999px;" id="M3" height="10.7375" version="1.1" viewBox="0 0 7.4749999 10.7375" width="7.4749999"  xmlns="http://www.w3.org/2000/svg">
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			<text transform="matrix(1,0,0,-1,-71.95,63.6)">
				<tspan style="font-size: 12.50px; " x="0" y="0">𝑏</tspan>
			</text>

		</g>
	</g>
</svg>]1,8-naphthyridines in high yields. The Bismuth(III) chloride is an environmentally friendly catalyst.

Tangali R. Ravikumar Naik

Halehatty S. Bhojya Naik

Halehatty R. Prakasha Naik

P. J. Bindu

Three-Component One-Pot Synthesis of Novel Benzo[<svg style="vertical-align:-0.1638pt" height="12.4375" version="1.1" viewBox="0 0 8.1000004 12.4375" width="8.1000004" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns="http://www.w3.org/2000/svg"><g transform="matrix(.017,-0,0,-.017,.062,12.162)"><path id="x1D44F" d="M452 333q0 -82 -46 -164t-116 -128q-81 -53 -158 -53q-26 0 -51 13t-37 32q-26 41 -6 134l91 431q7 40 2.5 47t-34.5 7h-33l2 25q36 4 72.5 13t58.5 15.5t28 6.5q10 0 4 -29l-91 -391h2q65 77 130 116.5t105 39.5q36 0 56.5 -32t20.5 -83zM365 316q0 76 -35 76&#xA;q-31 0 -93.5 -49t-107.5 -110q-12 -37 -17 -70q-9 -65 12 -96.5t59 -31.5q31 0 56 14q53 29 89.5 105t36.5 162z" /></g></svg>]1,8-naphthyridines Catalyzed by Bismuth(III) Chloride

Novel carbon-rich photochromic dihydroindolizine (DHI) derivatives substituted in the fluorene part (region A) in addition to the new spirocyclopropene 6 have been synthesized. The synthesis of dimethyl <svg style="vertical-align:-0.0pt;width:12.2875px;" id="M1" height="12.7625" version="1.1" viewBox="0 0 12.2875 12.7625" width="12.2875"  xmlns="http://www.w3.org/2000/svg">
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			</text>

		</g>
	</g>
</svg>,<svg style="vertical-align:-0.10033pt;width:12.2875px;" id="M2" height="12.6875" version="1.1" viewBox="0 0 12.2875 12.6875" width="12.2875"  xmlns="http://www.w3.org/2000/svg">
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			<text transform="matrix(1,0,0,-1,-71.95,62)">
				<tspan style="font-size: 12.50px; " x="0" y="0">7</tspan>
			</text>

			<text transform="matrix(1,0,0,-1,-65.7,67.01)">
				<tspan style="font-size: 8.75px; " x="0" y="0"></tspan>
			</text>

		</g>
	</g>
</svg>-diethynylspiro[cycloprop[2]ene-1,<svg style="vertical-align:-0.27588pt;width:12.2875px;" id="M3" height="13.1125" version="1.1" viewBox="0 0 12.2875 13.1125" width="12.2875"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,13.1125)">
		<g transform="translate(72,-61.51)">
			<text transform="matrix(1,0,0,-1,-71.95,61.84)">
				<tspan style="font-size: 12.50px; " x="0" y="0">9</tspan>
			</text>

			<text transform="matrix(1,0,0,-1,-65.7,67.01)">
				<tspan style="font-size: 8.75px; " x="0" y="0"></tspan>
			</text>

		</g>
	</g>
</svg>-fluorene]-2,3-dicarboxylate precursor <b  >6</b> was accomplished in five steps, starting with the literature known conversion of fluorene to 2,7-dibromo-9H-fluoren-9-one in 56&#x25; yield over three steps. The chemical structures of the new synthesized materials have been elucidated by both analytical and spectroscopic tools. Three alterative synthetic pathways for the synthesis of DHI 
<b  >9</b> have been established.

Saleh Abdel-Mgeed Ahmed

Photochromism of Dihydroindolizines Part XI: Synthesis of Novel Carbon-Rich Photochromic Dihydroindolizines-Based Potential Electronic Devices

Aza-conjugate addition of phthalimide to <svg style="vertical-align:-2.29482pt;width:24.174999px;" id="M2" height="13.425" version="1.1" viewBox="0 0 24.174999 13.425" width="24.174999"  xmlns="http://www.w3.org/2000/svg">
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				<tspan style="font-size: 12.50px; " x="7.0391889" y="0">,</tspan>
				<tspan style="font-size: 12.50px; " x="12.25294" y="0">𝛽</tspan>
			</text>

		</g>
	</g>
</svg>-unsaturated esters efficiently achieves in the presence of catalytic amount of <svg style="vertical-align:-3.25793pt;width:50.400002px;" id="M3" height="14.75" version="1.1" viewBox="0 0 50.400002 14.75" width="50.400002"  xmlns="http://www.w3.org/2000/svg">
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			<text transform="matrix(1,0,0,-1,-71.95,63.5)">
				<tspan style="font-size: 12.50px; " x="0" y="0">C</tspan>
				<tspan style="font-size: 12.50px; " x="8.3395014" y="0">s</tspan>
			</text>

			<text transform="matrix(1,0,0,-1,-58.75,60.37)">
				<tspan style="font-size: 8.75px; " x="0" y="0">2</tspan>
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				<tspan style="font-size: 12.50px; " x="0" y="0">C</tspan>
				<tspan style="font-size: 12.50px; " x="8.2394772" y="0">O</tspan>
			</text>

			<text transform="matrix(1,0,0,-1,-36.61,60.37)">
				<tspan style="font-size: 8.75px; " x="0" y="0">3</tspan>
			</text>

		</g>
	</g>
</svg> and ionic liquid 1-butyl-3-methylimidazolium bromide ([bmim]Br) under mild reaction conditions (<svg style="vertical-align:-0.17555pt;width:30.625px;" id="M4" height="11.0375" version="1.1" viewBox="0 0 30.625 11.0375" width="30.625"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,11.0375)">
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				<tspan style="font-size: 12.50px; " x="0" y="0">7</tspan>
				<tspan style="font-size: 12.50px; " x="6.2515001" y="0">0</tspan>
			</text>

			<text transform="matrix(1,0,0,-1,-59.45,68.56)">
				<tspan style="font-size: 8.75px; " x="0" y="0">∘</tspan>
			</text>

			<text transform="matrix(1,0,0,-1,-55.89,63.39)">
				<tspan style="font-size: 12.50px; " x="0" y="0">C</tspan>
			</text>

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	</g>
</svg>) to afford N-alkyl phthalimides in high yields and relatively short reaction times.

Alireza Hasaninejad

Abdolkarim Zare

Ahmad Reza Moosavi-Zare

Fatemeh Khedri

Rahimeh Rahimi

Ali Khalafi-Nezhad

<svg style="vertical-align:-3.39069pt" height="15.65" version="1.1" viewBox="0 0 54.462502 15.65" width="54.462502" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns="http://www.w3.org/2000/svg"><g transform="matrix(.017,-0,0,-.017,.062,11.362)"><path id="x43" d="M614 175l29 -10q-33 -109 -57 -154q-121 -26 -184 -26q-90 0 -160.5 29t-112.5 77t-63.5 105.5t-21.5 119.5q0 157 108 253t277 96q36 0 71.5 -5t69 -13.5t36.5 -8.5q15 -102 20 -150l-29 -8q-20 79 -66.5 114t-128.5 35q-119 0 -187.5 -86t-68.5 -207&#xA;q0 -140 73.5 -227.5t188.5 -87.5q73 0 119.5 37.5t86.5 116.5z" /></g><g transform="matrix(.017,-0,0,-.017,11.367,11.362)"><path id="x73" d="M319 325l-25 -7q-33 99 -103 99q-29 0 -47 -19.5t-18 -49.5t22 -49.5t62 -36.5q63 -26 95 -57t32 -79q0 -64 -50 -101t-115 -37q-35 0 -67.5 10.5t-46.5 23.5q-5 11 -11 51t-6 67l27 5q14 -53 46.5 -88.5t75.5 -35.5q29 0 50 19.5t21 50.5t-19.5 51.5t-59.5 39.5&#xA;q-28 12 -46 22.5t-38.5 27t-30.5 38.5t-10 49q0 54 42.5 92t109.5 38q48 0 88 -18q6 -15 13 -50.5t9 -55.5z" /></g><g transform="matrix(.012,-0,0,-.012,17.6,15.45)"><path id="x32" d="M412 140l28 -9q0 -2 -35 -131h-373v23q112 112 161 170q59 70 92 127t33 115q0 63 -31 98t-86 35q-75 0 -137 -93l-22 20l57 81q55 59 135 59q69 0 118.5 -46.5t49.5 -122.5q0 -62 -29.5 -114t-102.5 -130l-141 -149h186q42 0 58.5 10.5t38.5 56.5z" /></g><g transform="matrix(.017,-0,0,-.017,23.938,11.362)"><use xlink:href="#x43"/></g><g transform="matrix(.017,-0,0,-.017,35.361,11.362)"><path id="x4F" d="M381 665q131 0 226.5 -93t95.5 -239q0 -158 -96 -253t-238 -95q-137 0 -231 95t-94 238q0 142 92.5 244.5t244.5 102.5zM359 629q-89 0 -151 -74.5t-62 -208.5q0 -141 69 -233t175 -92q90 0 150.5 74t60.5 211q0 152 -69 237.5t-173 85.5z" /></g><g transform="matrix(.012,-0,0,-.012,48.062,15.45)"><path id="x33" d="M285 378v-2q65 -13 102 -54.5t37 -97.5q0 -57 -30.5 -104.5t-74 -75t-85.5 -42t-72 -14.5q-31 0 -59.5 11t-40.5 23q-19 18 -16 36q1 16 23 33q13 10 24 0q58 -51 124 -51q55 0 88 40t33 112q0 64 -39 96.5t-88 32.5q-29 0 -64 -11l-6 29q77 25 118 57.5t41 84.5&#xA;q0 45 -26.5 69.5t-68.5 24.5q-67 0 -120 -79l-20 20l43 63q51 56 127 56h1q66 0 107 -37t41 -95q0 -42 -31 -71q-22 -23 -68 -54z" /></g></svg>/[bmim]Br as an Efficient, Green, and Reusable Catalytic System for the Synthesis of N-Alkyl Derivatives of Phthalimide under Mild Conditions

Three series of novel formononetin derivatives were synthesized, in which formononetin and
heterocyclic moieties were separated by 2-carbon, 3-carbon, and 4-carbon spacers. The chemical
structures of these compounds were confirmed. All the derivatives were screened for antiproliferative
activities against Jurkat cell line and HepG-2 cell line. In this paper, compounds prepared were also
screened for their antibacterial activity of six bacterial strains. Compound 
<b  >3b</b> exihibited promising
antibacterial activity against <i  >B. subtilis</i> with minimal inhibitory concentration (MIC) value of 0.78&#x2009;<svg style="vertical-align:-2.29482pt;width:9.6374998px;" id="M1" height="9.6750002" version="1.1" viewBox="0 0 9.6374998 9.6750002" width="9.6374998"  xmlns="http://www.w3.org/2000/svg">
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			<text transform="matrix(1,0,0,-1,-71.95,66.6)">
				<tspan style="font-size: 12.50px; " x="0" y="0">𝜇</tspan>
			</text>

		</g>
	</g>
</svg>g/mL, and compound <b  >5e</b> showed significant antiproliferative activities against Jurkat cell growth
with <svg style="vertical-align:-3.25793pt;width:27.3125px;" id="M2" height="14.75" version="1.1" viewBox="0 0 27.3125 14.75" width="27.3125"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,14.75)">
		<g transform="translate(72,-60.2)">
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			</text>

			<text transform="matrix(1,0,0,-1,-59.45,60.37)">
				<tspan style="font-size: 8.75px; " x="0" y="0">5</tspan>
				<tspan style="font-size: 8.75px; " x="4.3759999" y="0">0</tspan>
			</text>

		</g>
	</g>
</svg> of <svg style="vertical-align:-0.3135pt;width:73.637497px;" id="M3" height="14.375" version="1.1" viewBox="0 0 73.637497 14.375" width="73.637497"  xmlns="http://www.w3.org/2000/svg">
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				<tspan style="font-size: 12.50px; " x="0" y="0">1</tspan>
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				<tspan style="font-size: 12.50px; " x="24.655916" y="0">×</tspan>
				<tspan style="font-size: 12.50px; " x="35.433502" y="0">1</tspan>
				<tspan style="font-size: 12.50px; " x="41.685001" y="0">0</tspan>
			</text>

			<text transform="matrix(1,0,0,-1,-24.01,66.03)">
				<tspan style="font-size: 8.75px; " x="0" y="0">−</tspan>
				<tspan style="font-size: 8.75px; " x="5.99512" y="0">4</tspan>
			</text>

		</g>
	</g>
</svg>&#x2009;<svg style="vertical-align:-2.29482pt;width:9.6374998px;" id="M4" height="9.6750002" version="1.1" viewBox="0 0 9.6374998 9.6750002" width="9.6374998"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,9.675)">
		<g transform="translate(72,-64.26)">
			<text transform="matrix(1,0,0,-1,-71.95,66.6)">
				<tspan style="font-size: 12.50px; " x="0" y="0">𝜇</tspan>
			</text>

		</g>
	</g>
</svg>g/mL. The preliminary investigation of structure-activity relationships (SARs)
was also discussed based on the obtained experimental data.

Ying Yang

Wen-Jun Mao

Huan-Qiu Li

Tao-Tao Zhu

Lei Shi

Peng-Cheng Lv

Hai-Liang Zhu

Synthesis and Biological Evaluation of 7-O-Modified Formononetin Derivatives

We have developed a novel and one-pot synthesis of 6-arylpyrimidine-4-ol by reacting commercially available alkyl 3-oxo-3-arylpropanoate with formamide in the presence of stoichiometric amount of ammonium acetate.

Jitendra M. Gajera

Shital N. Tondlekar

Laxmikant A. Gharat

A Novel and One-Pot Synthesis of 6-arylpyrimidin-4-ol

Decomposition of the complex <b  >4</b>, formed between the  <svg style="vertical-align:-0.1254pt;width:8.9375px;" id="M2" height="7.1750002" version="1.1" viewBox="0 0 8.9375 7.1750002" width="8.9375"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,7.175)">
		<g transform="translate(72,-66.26)">
			<text transform="matrix(1,0,0,-1,-71.95,66.44)">
				<tspan style="font-size: 12.50px; " x="0" y="0">𝛼</tspan>
			</text>

		</g>
	</g>
</svg>-tocopherol <i  >ortho</i>-quinone methide (<b  >2</b>) and NMMO, by fast heating from <svg style="vertical-align:-0.17555pt;width:41.337502px;" id="M3" height="11.0375" version="1.1" viewBox="0 0 41.337502 11.0375" width="41.337502"  xmlns="http://www.w3.org/2000/svg">
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				<tspan style="font-size: 12.50px; " x="0" y="0">−</tspan>
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				<tspan style="font-size: 12.50px; " x="14.816055" y="0">8</tspan>
			</text>

			<text transform="matrix(1,0,0,-1,-50.88,68.56)">
				<tspan style="font-size: 8.75px; " x="0" y="0">∘</tspan>
			</text>

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				<tspan style="font-size: 12.50px; " x="0" y="0">C</tspan>
			</text>

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	</g>
</svg> to <svg style="vertical-align:-0.17555pt;width:30.625px;" id="M4" height="11.0375" version="1.1" viewBox="0 0 30.625 11.0375" width="30.625"  xmlns="http://www.w3.org/2000/svg">
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				<tspan style="font-size: 12.50px; " x="0" y="0">7</tspan>
				<tspan style="font-size: 12.50px; " x="6.2515001" y="0">0</tspan>
			</text>

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				<tspan style="font-size: 8.75px; " x="0" y="0">∘</tspan>
			</text>

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				<tspan style="font-size: 12.50px; " x="0" y="0">C</tspan>
			</text>

		</g>
	</g>
</svg> in inert solvents produces a novel <svg style="vertical-align:-0.1254pt;width:8.9375px;" id="M5" height="7.1750002" version="1.1" viewBox="0 0 8.9375 7.1750002" width="8.9375"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,7.175)">
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				<tspan style="font-size: 12.50px; " x="0" y="0">𝛼</tspan>
			</text>

		</g>
	</g>
</svg>-tocopherol dimer with <svg style="vertical-align:-0.17555pt;width:22.987499px;" id="M6" height="11.0375" version="1.1" viewBox="0 0 22.987499 11.0375" width="22.987499"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,11.0375)">
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				<tspan style="font-size: 12.50px; " x="0" y="0">6</tspan>
				<tspan style="font-size: 12.50px; " x="6.2515001" y="0">𝐻</tspan>
			</text>

		</g>
	</g>
</svg>,<svg style="vertical-align:-0.0pt;width:30.799999px;" id="M7" height="10.6875" version="1.1" viewBox="0 0 30.799999 10.6875" width="30.799999"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,10.6875)">
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				<tspan style="font-size: 12.50px; " x="0" y="0">1</tspan>
				<tspan style="font-size: 12.50px; " x="6.2515001" y="0">2</tspan>
				<tspan style="font-size: 12.50px; " x="12.503" y="0">𝐻</tspan>
			</text>

		</g>
	</g>
</svg>-dibenzo[b,f][1,5]dioxocine structure (<b  >5</b>) which&#x2014;in contrast to the well-known spiro-dimer of <svg style="vertical-align:-0.1254pt;width:8.9375px;" id="M8" height="7.1750002" version="1.1" viewBox="0 0 8.9375 7.1750002" width="8.9375"  xmlns="http://www.w3.org/2000/svg">
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		<g transform="translate(72,-66.26)">
			<text transform="matrix(1,0,0,-1,-71.95,66.44)">
				<tspan style="font-size: 12.50px; " x="0" y="0">𝛼</tspan>
			</text>

		</g>
	</g>
</svg>-tocopherol (<b  >3</b>)&#x2014;is symmetrical. This is the first example of a direct reaction of the highly transient zwitterionic, aromatic precursor <b  >2a</b> in the formation of the <i  >ortho</i>-quinone 
methide <b  >2</b>.

Anjan Patel

Francesco Mazzini

Thomas Netscher

Thomas Rosenau

A Novel Dimer of <svg style="vertical-align:-0.1638pt" height="7.9499998" version="1.1" viewBox="0 0 9.7749996 7.9499998" width="9.7749996" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns="http://www.w3.org/2000/svg"><g transform="matrix(.017,-0,0,-.017,.062,7.675)"><path id="x1D6FC" d="M545 106q-67 -118 -134 -118q-24 0 -40 37.5t-30 129.5h-2q-47 -72 -103 -119.5t-108 -47.5q-47 0 -76 45.5t-29 119.5q0 113 85 204t174 91q47 0 70 -33.5t43 -119.5h3q32 47 80 140l55 13l10 -9q-47 -80 -138 -201q17 -99 27.5 -136t22.5 -37q23 0 69 61zM333 204&#xA;q-14 98 -31 149.5t-50 51.5q-49 0 -94 -70t-45 -164q0 -55 15.5 -86t40.5 -31q70 0 164 150z" /></g></svg>-Tocopherol

The direct conversion of solid-supported carboxylic acid allyl esters to carboxamides through the use of phenylsilane and catalytic Pd<svg style="vertical-align:-3.69682pt;width:47.950001px;" id="M1" height="15.4125" version="1.1" viewBox="0 0 47.950001 15.4125" width="47.950001"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,15.4125)">
		<g transform="translate(72,-59.67)">
			<text transform="matrix(1,0,0,-1,-71.95,63.41)">
				<tspan style="font-size: 12.50px; " x="0" y="0">(</tspan>
				<tspan style="font-size: 12.50px; " x="4.1634989" y="0">P</tspan>
				<tspan style="font-size: 12.50px; " x="11.12767" y="0">P</tspan>
				<tspan style="font-size: 12.50px; " x="18.091841" y="0">h</tspan>
			</text>

			<text transform="matrix(1,0,0,-1,-47.61,60.28)">
				<tspan style="font-size: 8.75px; " x="0" y="0">3</tspan>
			</text>

			<text transform="matrix(1,0,0,-1,-42.73,63.41)">
				<tspan style="font-size: 12.50px; " x="0" y="0">)</tspan>
			</text>

			<text transform="matrix(1,0,0,-1,-38.57,59.72)">
				<tspan style="font-size: 8.75px; " x="0" y="0">4</tspan>
			</text>

		</g>
	</g>
</svg> under mild reaction conditions is reported.  The use of this methodology for the generation of a 48 compound solid-phase array is described herein.

Zheming Ruan

Katy Van Kirk

Christopher B. Cooper

R. Michael Lawrence

A Novel, One-Step Palladium and Phenylsilane Activated Amidation from Allyl Ester on Solid Support

Per-<svg style="vertical-align:-0.13794pt;width:11.875px;" id="M1" height="10.75" version="1.1" viewBox="0 0 11.875 10.75" width="11.875"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,10.75)">
		<g transform="translate(72,-63.4)">
			<text transform="matrix(1,0,0,-1,-71.95,63.59)">
				<tspan style="font-size: 12.50px; " x="0" y="0">𝑂</tspan>
			</text>

		</g>
	</g>
</svg>-acetyl-5-thio-DL-mannose was synthesized from 
                  petrochemicals in six steps and 9&#x25; overall yield. It was then derivatized into glycosyl 
                  trichloroacetimidate and subjected to glycosidation reaction with a mannosyl acceptor to 
                  give a separatable mixture of disaccharides with 5-thio-D- and L-mannosides. This is the 
                  first synthesis of an enantiomerically pure 5-thiosugar derivative from racemic chemicals. 
                  The D-glycoside was derivatized into methyl 
                  (5-thio-<svg style="vertical-align:-0.1254pt;width:8.9375px;" id="M2" height="7.1750002" version="1.1" viewBox="0 0 8.9375 7.1750002" width="8.9375"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,7.175)">
		<g transform="translate(72,-66.26)">
			<text transform="matrix(1,0,0,-1,-71.95,66.44)">
				<tspan style="font-size: 12.50px; " x="0" y="0">𝛼</tspan>
			</text>

		</g>
	</g>
</svg>-D-mannopyranosyl)-2-<svg style="vertical-align:-0.13794pt;width:11.875px;" id="M3" height="10.75" version="1.1" viewBox="0 0 11.875 10.75" width="11.875"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,10.75)">
		<g transform="translate(72,-63.4)">
			<text transform="matrix(1,0,0,-1,-71.95,63.59)">
				<tspan style="font-size: 12.50px; " x="0" y="0">𝑂</tspan>
			</text>

		</g>
	</g>
</svg>-<svg style="vertical-align:-0.1254pt;width:8.9375px;" id="M4" height="7.1750002" version="1.1" viewBox="0 0 8.9375 7.1750002" width="8.9375"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,7.175)">
		<g transform="translate(72,-66.26)">
			<text transform="matrix(1,0,0,-1,-71.95,66.44)">
				<tspan style="font-size: 12.50px; " x="0" y="0">𝛼</tspan>
			</text>

		</g>
	</g>
</svg>-D-mannopyranoside 6-phosphate as a potential inhibitor 
                  of a golgi <svg style="vertical-align:-0.1254pt;width:8.9375px;" id="M5" height="7.1750002" version="1.1" viewBox="0 0 8.9375 7.1750002" width="8.9375"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,7.175)">
		<g transform="translate(72,-66.26)">
			<text transform="matrix(1,0,0,-1,-71.95,66.44)">
				<tspan style="font-size: 12.50px; " x="0" y="0">𝛼</tspan>
			</text>

		</g>
	</g>
</svg>-1,2-mannosidase.

Hideya Yuasa

Masatake Jouyabu

Nobuyuki Mitsuhashi

Hironobu Hashimoto

Syntheses of 5-Thio-D-Mannose from Petrochemicals and a Disaccharide Analog Containing It

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Organic Chemistry International